United States, et al. v. CVS Health Corporation and Aetna Inc.; Response to Public Comments, 5466-5477 [2019-02846]
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5466
Federal Register / Vol. 84, No. 35 / Thursday, February 21, 2019 / Notices
hours by 50 and 12.5 (13) hours
respectively, since the previous renewal
in 2016.
If additional information is required
contact: Melody Braswell, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, 3E.405A,
Washington, DC 20530.
Dated: February 15, 2019.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2019–02936 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–FY–P
DEPARTMENT OF JUSTICE
Bureau of Alcohol, Tobacco, Firearms
and Explosives
[OMB Number 1140–0066]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Revision of a
Currently Approved Collection;
Manufacturers of Ammunition,
Records and Supporting Data of
Ammunition Manufactured and
Disposed of
Bureau of Alcohol, Tobacco,
Firearms and Explosives, Department of
Justice
ACTION: 60-Day notice.
AGENCY:
The Department of Justice
(DOJ), Bureau of Alcohol, Tobacco,
Firearms and Explosives (ATF), will
submit the following information
collection request to the Office of
Management and Budget (OMB) for
review and approval in accordance with
the Paperwork Reduction Act of 1995.
The proposed collection OMB 1140–
0066 (Manufacturers of Ammunition,
Records and Supporting Data of
Ammunition Manufactured and
Disposed of) is being revised due to a
change in burden, since there is an
increase in the number of responses to
this information collection, which has
also caused an increase in the total
collection burden hours.
DATES: Comments are encouraged and
will be accepted for 60 days until April
22, 2019.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments,
regarding the estimated public burden
or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions, or
additional information, please contact:
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SUMMARY:
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Jason Gluck, ATF Firearms Industry
Programs Branch, either by mail at 99
New York Ave. NE, Washington, DC
20226, by email at Fipbinformationcollection@atf.gov, or by
telephone at 202–648–7190.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Evaluate whether and if so how the
quality, utility, and clarity of the
information to be collected can be
enhanced; and
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
respondents may utilize this
information collection to provide a total
188 responses, and it will take each
respondent 2 minutes to provide their
response.
6. An estimate of the total public
burden (in hours) associated with the
collection: The estimated annual public
burden associated with this collection is
6.2 (6) hours, which is equal to 376
(total # of respondents) * .5 (total # of
responses per respondents) * .033 (2
minutes).
7. An Explanation of the Change in
Estimates: The changes in burden are
due to an increase in the number of
responses to this collection from 159
during the last renewal in 2016, to 188
currently. Consequently, the burden
hours for this information collection has
also increased slightly from 5 to 6.2 (6)
hours respectively.
If additional information is required
contact: Melody Braswell, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, 3E.405A,
Washington, DC 20530.
Dated: February 15, 2019.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2019–02935 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–FY–P
Overview of This Information
Collection
DEPARTMENT OF JUSTICE
1. Type of Information Collection:
Revision of a currently approved
collection.
2. The Title of the Form/Collection:
Manufacturers of Ammunition, Records
and Supporting Data of Ammunition
Manufactured and Disposed of.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
Form number (if applicable): None.
Component: Bureau of Alcohol,
Tobacco, Firearms and Explosives, U.S.
Department of Justice.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Primary: Business or other for-profit.
Other (if applicable): None.
Abstract: The manufacturer’s records
are used by ATF in criminal
investigations and compliance
inspections, to fulfill the Bureau’s
mission to enforce the Gun Control Law.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: About half of an estimated 376
Antitrust Division
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United States, et al. v. CVS Health
Corporation and Aetna Inc.; Response
to Public Comments
Pursuant to the Antitrust Procedures
and Penalties Act, 15 U.S.C. 16(b)–(h),
the United States hereby publishes
below the Response to Public Comments
on the Proposed Final Judgment in
United States, et al. v. CVS Health
Corporation and Aetna Inc., Civil
Action No. 1:18–cv–02340, which was
filed in the United States District Court
for the District of Columbia on February
13, 2019, together with copies of the 173
comments received by the United
States.
Pursuant to the Court’s February 9,
2019 order, comments were published
electronically and are available to be
viewed and downloaded at the Antitrust
Division’s Web site, at: https://
www.justice.gov/atr/us-v-cvs-healthcorp-and-aetna-inc-index-comments. A
copy of the United States’ response to
the comments is also available at the
same location. Copies of the comments
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and the United States’ response are
available for inspection at the Office of
the Clerk of the United States District
Court for the District of Columbia.
Copies of these materials may also be
obtained from the Antitrust Division
upon request and payment of the
copying fee set by Department of Justice
regulations.
Patricia A. Brink,
Director of Civil Enforcement.
5467
Case No. 1:18–cv–02340–RJL
RESPONSE OF PLAINTIFF UNITED
STATES TO PUBLIC COMMENTS ON
THE PROPOSED FINAL JUDGMENT
United States District Court for the
District of Columbia
United States of America et al., Plaintiffs,
v. CVS Health Corporation and AETNA Inc.,
Defendants.
TABLE OF CONTENTS
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I. Introduction .........................................................................................................................................................................................
II. Procedural History .............................................................................................................................................................................
III. Standard of Judicial Review .............................................................................................................................................................
IV. The Investigation, the Harm Alleged in the Complaint, and the Proposed Final Judgment .......................................................
V. Summary of Public Comments and the United States’ Response ..................................................................................................
A. Comments Regarding WellCare’s Suitability as a Divestiture Buyer and Ability to Compete Effectively ...........................
1. WellCare is an experienced and effective competitor .......................................................................................................
2. WellCare is an independent competitor to CVS ................................................................................................................
3. Prior health insurance merger remedies do not cast doubt on the divestiture ...............................................................
4. The remedy does not create new structural concerns in the markets for individual PDPs ...........................................
5. The licensing provisions related to the Aetna brand protect WellCare’s ability to compete using the divested assets
6. The sales price does not cast doubt on WellCare’s intention to compete .......................................................................
B. Comments Related to the Vertical Aspects of CVS’s Acquisition of Aetna ............................................................................
1. Input foreclosure is unlikely to occur and is beyond the scope of the Complaint .........................................................
2. Customer foreclosure is unlikely to occur and is beyond the scope of the Complaint ..................................................
3. Vertical concerns are not addressable under the Tunney Act’s standard of review .......................................................
C. Other Miscellaneous Comments ................................................................................................................................................
D. Comments in Support of the Merger .........................................................................................................................................
VI. Conclusion ........................................................................................................................................................................................
I. Introduction
As required by the Antitrust
Procedures and Penalties Act (the
‘‘APPA’’ or ‘‘Tunney Act’’), 15 U.S.C. §§
16(b)–(h), the United States hereby
responds to the public comments
received about the proposed Final
Judgment in this case. After careful
consideration of the comments, the
United States continues to believe that
the proposed remedy will address the
harm alleged in the Complaint and is
therefore in the public interest.
The remedy preserves competition for
the approximately 21 million
beneficiaries who purchase individual
prescription drug plans (‘‘individual
PDPs’’) in the United States. The
remedy fully addresses the competitive
threat posed by the merger by requiring
CVS to divest Aetna’s nationwide
individual PDP business to WellCare
Health Plans, Inc., an experienced
health insurer focused on governmentsponsored health plans, including
individual PDPs. By requiring a
nationwide divestiture, the remedy
provides WellCare with the assets and
scale necessary to maintain competition
in the 16 regions identified in the
Complaint. The remedy also provides
WellCare with access to all of the
records, employees, and other rights
necessary to ensure that WellCare can
step into Aetna’s shoes. The remedy
thus preserves the competition that
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otherwise would be lost through the
merger and ensures that WellCare will
effectively replace Aetna as an
independent and vigorous competitor.
The United States received 173
comments about the proposed remedy
reflecting a wide range of views. Some
comments supported the merger. Other
comments acknowledged the significant
scope of the divestiture, but expressed
concerns about the divestiture buyer.
Many comments raised issues that are
outside the scope of the Tunney Act
review. After careful consideration of
these comments, the United States
maintains that the remedy in the
proposed Final Judgment provides
comprehensive relief that satisfies the
Tunney Act’s public-interest standard.
The United States will publish the
comments and this response on the
Antitrust Division’s website and is
submitting to the Federal Register this
response and the website address at
which the comments may be viewed
and downloaded, as authorized by the
Court’s order dated February 9, 2019.
Following Federal Register publication,
the United States will move the Court to
enter the proposed Final Judgment.
II. Procedural History
On December 3, 2017, CVS entered
into an agreement to acquire Aetna in a
merger valued at approximately $69
billion. On October 10, 2018, the United
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2
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States filed a civil antitrust Complaint
seeking to enjoin CVS from acquiring
Aetna because the proposed acquisition
would substantially lessen competition
for the sale of individual PDPs in 16
regions in the United States in violation
of Section 7 of the Clayton Act, 15
U.S.C. § 18.
Simultaneously with the filing of the
Complaint, the United States filed a
proposed Final Judgment, a Stipulation
signed by the parties that consents to
entry of the proposed Final Judgment
after compliance with the requirements
of the Tunney Act, and a Competitive
Impact Statement describing the
transaction and the proposed Final
Judgment. The United States caused the
Complaint, the proposed Final
Judgment, and Competitive Impact
Statement to be published in the Federal
Register on October 17, 2018, see 83
Fed. Reg. 52558 (October 17, 2018), and
caused notice regarding the same,
together with directions for the
submission of written comments
relating to the proposed Final Judgment,
to be published in The Washington Post
on October 12–18, 2018. The 60-day
period for public comment ended on
December 17, 2018.
III. Standard of Judicial Review
The Clayton Act, as amended by the
APPA, requires that proposed consent
judgments in antitrust cases brought by
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the United States be subject to a 60-day
comment period, after which the court
shall determine whether entry of the
proposed Final Judgment ‘‘is in the
public interest.’’ 15 U.S.C. § 16(e)(1). In
making that determination, the court, in
accordance with the statute as amended
in 2004, is required to consider:
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(A) the competitive impact of such
judgment, including termination of alleged
violations, provisions for enforcement and
modification, duration of relief sought,
anticipated effects of alternative remedies
actually considered, whether its terms are
ambiguous, and any other competitive
considerations bearing upon the adequacy of
such judgment that the court deems
necessary to a determination of whether the
consent judgment is in the public interest;
and
(B) the impact of entry of such judgment
upon competition in the relevant market or
markets, upon the public generally and
individuals alleging specific injury from the
violations set forth in the complaint
including consideration of the public benefit,
if any, to be derived from a determination of
the issues at trial.
15 U.S.C. § 16(e)(1)(A) & (B). In
considering these statutory factors, the
court’s inquiry is necessarily a limited
one as the government is entitled to
‘‘broad discretion to settle with the
defendant within the reaches of the
public interest.’’ United States v.
Microsoft Corp., 56 F.3d 1448, 1461
(D.C. Cir. 1995); see generally United
States v. SBC Commc’ns, Inc., 489 F.
Supp. 2d 1 (D.D.C. 2007) (assessing
public-interest standard under the
Tunney Act); United States v. U.S.
Airways Group, Inc., 38 F. Supp. 3d 69,
75 (D.D.C. 2014) (explaining that the
‘‘court’s inquiry is limited’’ in Tunney
Act settlements); United States v. InBev
N.V./S.A., No. 08-1965 (JR), 2009 U.S.
Dist. LEXIS 84787, at *3 (D.D.C. Aug.
11, 2009) (noting that the court’s review
of a consent judgment is limited and
only inquires ‘‘into whether the
government’s determination that the
proposed remedies will cure the
antitrust violations alleged in the
complaint was reasonable, and whether
the mechanism to enforce the final
judgment are clear and manageable’’).
As the U.S. Court of Appeals for the
District of Columbia Circuit has held,
under the APPA a court considers,
among other things, the relationship
between the remedy secured and the
specific allegations in the government’s
complaint, whether the decree is
sufficiently clear, whether its
enforcement mechanisms are sufficient,
and whether the decree may positively
harm third parties. See Microsoft, 56
F.3d at 1458–62. With respect to the
adequacy of the relief secured by the
decree, a court may not ‘‘engage in an
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unrestricted evaluation of what relief
would best serve the public.’’ United
States v. BNS, Inc., 858 F.2d 456, 462
(9th Cir. 1988) (quoting United States v.
Bechtel Corp., 648 F.2d 660, 666 (9th
Cir. 1981)); see also Microsoft, 56 F.3d
at 1460–62; United States v. Alcoa, Inc.,
152 F. Supp. 2d 37, 40 (D.D.C. 2001);
InBev, 2009 U.S. Dist. LEXIS 84787, at
*3. Instead:
[t]he balancing of competing social and
political interests affected by a proposed
antitrust consent decree must be left, in the
first instance, to the discretion of the
Attorney General. The court’s role in
protecting the public interest is one of
insuring that the government has not
breached its duty to the public in consenting
to the decree. The court is required to
determine not whether a particular decree is
the one that will best serve society, but
whether the settlement is ‘‘within the reaches
of the public interest.’’ More elaborate
requirements might undermine the
effectiveness of antitrust enforcement by
consent decree.
Bechtel, 648 F.2d at 666 (emphasis
added) (citations omitted).1
In determining whether a proposed
settlement is in the public interest, a
district court ‘‘must accord deference to
the government’s predictions about the
efficacy of its remedies, and may not
require that the remedies perfectly
match the alleged violations.’’ SBC
Commc’ns, 489 F. Supp. 2d at 17; see
also U.S. Airways, 38 F. Supp. 3d at 74–
75 (noting that a court should not reject
the proposed remedies because it
believes others are preferable and that
room must be made for the government
to grant concessions in the negotiation
process for settlements); Microsoft, 56
F.3d at 1461 (noting the need for courts
to be ‘‘deferential to the government’s
predictions as to the effect of the
proposed remedies’’); United States v.
Archer-Daniels-Midland Co., 272 F.
Supp. 2d 1, 6 (D.D.C. 2003) (noting that
the court should grant ‘‘due respect to
the government’s prediction as to the
effect of proposed remedies, its
perception of the market structure, and
its views of the nature of the case’’). The
ultimate question is whether ‘‘the
remedies [obtained in the decree are] so
inconsonant with the allegations
charged as to fall outside of the ‘reaches
of the public interest.’ ’’ Microsoft, 56
F.3d at 1461 (quoting United States v.
Western Elec. Co., 900 F.2d 283, 309
(D.C. Cir. 1990)). To meet this standard,
1 See also BNS, 858 F.2d at 464 (holding that the
court’s ‘‘ultimate authority under the [APPA] is
limited to approving or disapproving the consent
decree’’); United States v. Gillette Co., 406 F. Supp.
713, 716 (D. Mass. 1975) (noting that, in this way,
the court is constrained to ‘‘look at the overall
picture not hypercritically, nor with a microscope,
but with an artist’s reducing glass’’).
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the United States ‘‘need only provide a
factual basis for concluding that the
settlements are reasonably adequate
remedies for the alleged harms.’’ SBC
Commc’ns, 489 F. Supp. 2d at 17.
Moreover, under Microsoft, the court’s
role under the APPA is limited to
reviewing the remedy in relationship to
the violations that the United States has
alleged in its complaint, and does not
authorize the court to ‘‘construct [its]
own hypothetical case and then
evaluate the decree against that case.’’
Microsoft, 56 F.3d at 1459; see also U.S.
Airways, 38 F. Supp. 3d at 75 (noting
that the court must simply determine
whether there is a factual foundation for
the government’s decisions such that its
conclusions regarding the proposed
settlements are reasonable); InBev, 2009
U.S. Dist. LEXIS 84787, at *20 (‘‘the
‘public interest’ is not to be measured by
comparing the violations alleged in the
complaint against those the court
believes could have, or even should
have, been alleged’’). Because the
‘‘court’s authority to review the decree
depends entirely on the government’s
exercising its prosecutorial discretion by
bringing a case in the first place,’’ it
follows that ‘‘the court is only
authorized to review the decree itself,’’
and not to ‘‘effectively redraft the
complaint’’ to inquire into other matters
that the United States did not pursue.
Microsoft, 56 F.3d at 1459–60. To
inquire about claims that are not in a
complaint would violate the separation
of powers and aggravate the
‘‘constitutional difficulties that inhere
in this statute.’’ See United States’
December 14, 2018 Response to Order to
Show Cause, Dkt. #32 at 3–7 (discussing
the constitutional difficulties with the
Tunney Act); see also Microsoft 56 F.3d
at 1459; United States v. Fokker Servs.,
818 F.3d 733, 738 (D.C. Cir. 2016)
(recognizing the ‘‘long-settled
understandings about the independence
of the Executive with regard to charging
decisions’’); Heckler v. Chaney, 470 U.S.
821, 832 (1985) (quoting U.S. Const. art.
II, § 3) (recognizing that the decision
about which claims to bring ‘‘has long
been regarded as the special province of
the Executive Branch.’’).
An amicus brief filed by the AIDS
Healthcare Foundation erroneously
argues that the 2004 amendments to the
Tunney Act overrule Microsoft,
allowing courts to consider allegations
that are not in the complaint.2 In fact,
however, the amendments addressed a
separate issue. In the Microsoft opinion,
after the court held that the Tunney Act
does not allow courts to look beyond the
2 Amicus Brief from the AIDS Healthcare
Foundation, Dkt. #50-1.
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scope of the complaint, the opinion says
that a district judge is not obliged to
accept a consent decree that ‘‘appears to
make a mockery of judicial power.’’ 56
F.3d at 1462. According to legislative
history of the 2004 amendments,
Congress was concerned that
subsequent courts had taken this latter
language too far, limiting their review
solely to the question of whether
‘‘antitrust consent judgments’’ would
make ‘‘a mockery of the judicial
function.’’ 3 As a result, Congress
changed the language of § 16(e) from
saying that the court ‘‘may’’ consider the
public-interest factors to the court
‘‘shall’’ consider those factors, making
them mandatory.4 Congress also
modified the list of factors, for example,
adding a new factor (whether the terms
of the judgment are ambiguous 5), which
the Microsoft court had already made
clear was appropriate to consider, 56
F.3d at 1461–62. Thus, as Senator Hatch
observed, ‘‘this amendment essentially
codifies existing case law.’’ 6 See also
SBC Commc’ns, 489 F. Supp. 2d at 11
(concluding that the 2004 amendments
‘‘effected minimal changes’’ to the
Tunney Act review).
Indeed, rather than overruling
Microsoft, the 2004 amendments
reaffirm that courts should focus solely
on how the judgment impacts the harms
alleged in the complaint by (1) keeping
the language in § 16(e) that directs
courts to limit their analysis to the
competitive impact of the ‘‘consent
judgment,’’ 7 (2) adding language that
directs courts to consider competition
‘‘in the relevant market or markets,’’ 8
and (3) making those considerations
mandatory rather than permissive. As
Senator Kohl’s floor statement
explained, ‘‘A mandate to review the
impact of entry of the consent judgment
upon ‘competition in the relevant
market or markets’ . . . will ensure that
the Tunney Act review is properly
focused on the likely competitive
impact of the judgment, rather than
extraneous factors irrelevant to the
purposes of antitrust enforcement.’’ 9
3 Antitrust Criminal Penalty Enhancement and
Reform Act of 2004, Pub. L. No. 108-237, tit. II, §
221(a), 118 Stat. 661, 668 (2004) (finding that ‘‘it
would misconstrue the meaning and Congressional
intent in enacting the Tunney Act to limit the
discretion of district courts to review antitrust
consent judgments solely to determining whether
entry of those consent judgments would make a
‘mockery of the judicial function.’ ’’).
4 Compare 15 U.S.C. § 16(e) (2004), with 15 U.S.C.
§ 16(e)(1) (2006).
5 15 U.S.C. § 16 (e)(1)(A).
6 150 Cong. Rec. S3610, at S3613 (daily ed. Apr.
2, 2004).
7 15 U.S.C. § 16(e)(1).
8 Compare 15 U.S.C. § 16(e) (2004), with 15 U.S.C.
§ 16(e)(1)(B) (2006).
9 150 Cong. Rec. S3618 (statement of Sen. Kohl).
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Finally, in the 2004 amendments,
Congress addressed the Tunney Act
review process, adding the
unambiguous instruction that ‘‘[n]othing
in this section shall be construed to
require the court to conduct an
evidentiary hearing or to require the
court to permit anyone to intervene.’’ 15
U.S.C. § 16(e)(2); see also U.S. Airways,
38 F. Supp. 3d at 76 (indicating that a
court is not required to hold an
evidentiary hearing or to permit
intervenors as part of its review under
the Tunney Act). This language
explicitly wrote into the statute what
Congress intended when it first enacted
the Tunney Act in 1974. As Senator
Tunney explained: ‘‘[t]he court is
nowhere compelled to go to trial or to
engage in extended proceedings which
might have the effect of vitiating the
benefits of prompt and less costly
settlement through the consent decree
process.’’ 119 Cong. Rec. 24,598 (1973)
(statement of Sen. Tunney). Rather, the
procedure for the public-interest
determination is left to the discretion of
the court, with the recognition that the
court’s ‘‘scope of review remains
sharply proscribed by precedent and the
nature of Tunney Act proceedings.’’
SBC Commc’ns, 489 F. Supp. 2d at 11.
A court can make its public-interest
determination based on the competitive
impact statement and response to public
comments alone. U.S. Airways, 38 F.
Supp. 3d at 76; see also United States
v. Enova Corp., 107 F. Supp. 2d 10, 17
(D.D.C. 2000) (noting that the ‘‘Tunney
Act expressly allows the court to make
its public interest determination on the
basis of the competitive impact
statement and response to comments
alone’’); S. Rep. No. 93-298 93d Cong.,
1st Sess., at 6 (1973) (‘‘Where the public
interest can be meaningfully evaluated
simply on the basis of briefs and oral
arguments, that is the approach that
should be utilized.’’).
IV. The Investigation, the Harm Alleged
in the Complaint, and the Proposed
Final Judgment
The proposed Final Judgment is the
culmination of a thorough,
comprehensive investigation conducted
by the Antitrust Division of the U.S.
Department of Justice into CVS’s
proposed acquisition of Aetna. As noted
in the Complaint, CVS is one of the
largest companies in the United States.
It operates the nation’s largest retail
pharmacy chain. It owns a large
pharmacy benefit manager (‘‘PBM’’)
called Caremark, which manages the
pharmacy benefits for various health
plans and negotiates their drug pricing
with pharmaceutical companies and
retail pharmacies. Through its
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5469
subsidiary called SilverScript, CVS is
also the nation’s largest provider of
individual PDPs, which provide
Medicare beneficiaries with insurance
coverage for their prescription drugs.
Aetna is the nation’s third largest health
insurer and, before the divestiture,
offered individual PDPs throughout the
United States.
Based on the evidence gathered
during its investigation, the United
States concluded that CVS’s proposed
acquisition of Aetna would likely
substantially lessen competition for the
sale of individual PDPs in the 16
geographic regions where CVS and
Aetna are particularly strong, resulting
in higher prices, less innovation, fewer
choices, and lower-quality individual
PDPs for Medicare beneficiaries in these
regions. Accordingly, the United States
filed a civil antitrust lawsuit to block
the acquisition as a violation of Section
7 of the Clayton Act, 15 U.S.C. § 18.
The proposed Final Judgment
provides an effective and appropriate
remedy for the transaction’s likely
competitive harm by requiring CVS to
divest Aetna’s individual PDP business
nationwide. The proposed Final
Judgment has several components,
which the parties agreed to abide by
during the pendency of the Tunney Act
proceeding, and which the Court
ordered in the Asset Preservation
Stipulation and Order of October 25,
2018, Dkt. # 15.
First, CVS must divest both of Aetna’s
individual PDP contracts with the
Centers for Medicare and Medicaid
Services (‘‘CMS’’), which is the federal
agency that administers the PDP
program. Aetna’s individual PDP
business was the only portion of Aetna’s
business where the merger with CVS
would have caused a substantial
lessening of competition. Divesting
Aetna’s nationwide individual PDP
business—and not just Aetna’s business
in the regions identified in the
Complaint—provides WellCare with the
same scale and capabilities to
implement a national PDP strategy as
Aetna had before the merger. Aetna’s
individual PDP contracts were
transferred to WellCare on November
29, 2018. From December 2018 to
January 2019, WellCare’s enrollment in
its legacy PDP plans increased by over
400,000 members nationwide, and its
market share grew in all 34 PDP regions.
The enrollment in the divested Aetna
plans also grew, adding over 140,000
members.10
10 See CMS Monthly Enrollment by CPSC for
January 2019, available at https://www.cms.gov/
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Second, the proposed Final Judgment
requires CVS and Aetna to transfer to
WellCare (1) data relating to Aetna’s
individual PDP business, (2)
information regarding the amount that
Aetna pays to retail pharmacies in
exchange for filling prescriptions for
Aetna members, and (3) any contracts
with brokers that currently sell Aetna’s
individual PDPs. The transfer of this
data, information, and contracts helps
ensure that WellCare has sufficient
information to negotiate with retail
pharmacies and brokers on the same
footing as Aetna did before the merger.
Third, during the 60-day period
following the sale to WellCare, the
proposed Final Judgment has provided
WellCare the opportunity to interview
and hire Aetna’s current employees
with expertise related to the individual
PDP business. The transfer of data and
recruiting of Aetna employees are
moving forward according to the terms
of the proposed Final Judgment.
The proposed Final Judgment also
includes provisions aimed at ensuring
that the divested assets are handed off
in a seamless and efficient manner,
particularly for the two key competitive
events for individual PDPs: the
submission of bids to CMS each June
(for the following year) and openenrollment season for members, which
occurs from October through December.
In this case, before the contracts were
transferred to WellCare on November
29, 2018, Aetna had already submitted
its bids for the divestiture assets and
open-enrollment was well under way.
Thus, to assist WellCare during the 2019
plan year, CVS must, at WellCare’s
option, enter into an administrative
services agreement to provide WellCare
with all of the services required to
manage the divestiture assets through
the plan year, which ends on December
31, 2019. These services include
contracting with pharmacy networks,
administering the plans’ formularies,
and providing back-office support and
claims administration functions.
Requiring CVS to support and service
these plans provides continuity to
members who purchased an Aetna
individual PDP during the openenrollment period that ran from October
through December 2018 and will ensure
that members receive the plans that they
have chosen. CVS and WellCare have
entered into an administrative services
agreement and, since the divestiture,
CVS has been providing WellCare with
the necessary services to manage the
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divestiture assets in 2019 while
WellCare has begun preparing for the
June 2019 submission of its bid for
2020.
Additionally, CVS and Aetna must
allow WellCare to use the Aetna brand
for the divestiture assets through
December 31, 2019, and CVS and Aetna
are prohibited, through 2020, from using
the Aetna brand for the CVS individual
PDP business that they are retaining.
This will provide WellCare with a
window to establish a relationship with
current Aetna individual PDP
beneficiaries and avoid customer
confusion.
The proposed Final Judgment also
includes robust mechanisms that will
allow the United States and the Court to
monitor the effectiveness of the relief
and to enforce compliance. For
example, the proposed Final Judgment
provides for the appointment of a
monitoring trustee, which the Court
appointed on December 3, 2018. As a
result, the monitoring trustee, Ms. Julie
Myers Wood, is actively working to
ensure that the divestiture proceeds
appropriately. She has the power and
authority to investigate and report on
Defendants’ compliance with the terms
of the Final Judgment and the Asset
Preservation Stipulation and Order
during the pendency of the divestiture
and is required to file reports with the
United States every 90 days. In addition,
the proposed Final Judgment provides
the United States with the ability to
investigate Defendants’ compliance with
the Final Judgment and expressly
retains and reserves all rights for the
United States to enforce the provisions
of the proposed Final Judgment,
including its rights to seek an order of
contempt from the Court.
Together, the requirements in the
proposed Final Judgment ensure that
WellCare can step into Aetna’s shoes,
thereby preserving the competition that
the merger would otherwise destroy.
V. Summary of Public Comments and
the United States’ Response
The United States received 173
comments 11 from different categories of
commenters. These commenters
included advocacy groups, such as the
American Medical Association
11 These comments are provided as attachments
TC-001 through TC-085. Aside from redactions of
personally identifiable information such as personal
email addresses, phone numbers, and patient
information, the comments are provided in their
entirety. Four groups of substantially similar
comments are included together as attachments TC007, TC-020, TC-057 and TC-061. Amicus filings
made before the end of the comment period by (1)
Consumer Action and U.S. PIRG and (2) PUTT and
PSSNY are included as attachments TC-023 and TC060, respectively.
PO 00000
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(‘‘AMA’’), the American Antitrust
Institute (‘‘AAI’’), Consumer Action and
U.S. PIRG, and the Medical Society of
the State of New York (‘‘MSSNY’’). In
addition, the United States received
comments from several groups
representing pharmacists that compete
with CVS, including the National
Community Pharmacists Association
(‘‘NCPA’’), the Pharmacists Society of
the State of New York (‘‘PSSNY’’), and
Pharmacists United for Truth and
Transparency (‘‘PUTT’’), as well as
approximately 120 individual
pharmacies. The United States also
received a handful of comments from
business associations and healthcare
industry associations.
The comments can be grouped into
four categories: (1) comments about
WellCare’s suitability as a divestiture
buyer, including whether it will have
sufficient assets, expertise, and
incentives to preserve competition; (2)
comments related to the vertical
combination of CVS’s pharmacy and
PBM businesses with Aetna’s health
insurance businesses; (3) other
miscellaneous comments, including
questions about whether the merger will
facilitate coordination, have
anticompetitive effects in various
healthcare markets, increase entry
barriers in the PBM or health insurance
markets, or reduce PBM competition by
eliminating Aetna as a PBM competitor;
and (4) comments in support of the
merger. The Court’s analysis under the
Tunney Act should focus on the first
category of comments, as they are the
only comments that relate to whether
the proposed remedy addresses the
harms alleged in the Complaint. See
Microsoft, 56 F.3d at 1459.
A. Comments Regarding WellCare’s
Suitability as a Divestiture Buyer and
Ability to Compete Effectively
WellCare has extensive experience
and qualifications in the individual PDP
market and, with the assets provided by
the proposed Final Judgment, is a
suitable divestiture buyer. Although the
AMA, Consumer Action and U.S. PIRG,
NCPA, PUTT and PSSNY, and
numerous independent pharmacies,
raised concerns regarding WellCare as
the buyer of the divested assets, none of
those concerns is valid for the reasons
explained below.12 These commenters
raised six primary objections: (1)
WellCare will not compete as effectively
as Aetna; (2) WellCare will not operate
independently of CVS because WellCare
uses CVS’s PBM, Caremark; (3) some
12 TC-003, TC-015, TC-023, TC-024, TC-047, TC054, TC-059, TC-060, TC-061, TC-063, TC-064, TC072, TC-080, TC-081, and TC-085.
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health insurance divestitures have not
been successful, indicating that the
divestiture to WellCare may not be
successful; (4) the divestiture creates
new structural concerns in the markets
for the sale of individual PDPs; (5) the
divestiture raises concerns related to
WellCare’s license of the Aetna brand;
and (6) the divestiture sales price is too
low.
1. WellCare is an experienced and
effective competitor.
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WellCare has experience and
qualifications in government-funded
insurance programs. Despite this,
commenters said that WellCare may not
compete as effectively as Aetna in
individual PDP markets because
WellCare is smaller and less capable
than Aetna and because WellCare is not
purchasing a stand-alone business unit;
these concerns are misplaced.13
Although Aetna’s overall membership is
larger when taking into account its
commercial business, WellCare is
already a large and established insurer
that has competed in the markets for
individual PDPs for over a decade.
WellCare is a Fortune 200 company
with over 12,000 employees, 5.5 million
members, and a market capitalization of
approximately $15 billion. Even before
acquiring over 2.1 million members
from Aetna as part of the divested
business, WellCare had attracted nearly
1.1 million individuals in its PDPs
throughout the United States. WellCare
is thus starting from a strong base and
its acquisition of all of Aetna’s
individual PDP business will enable
WellCare to improve its PDP business
and become a more significant
competitor.
Some commenters expressed a
concern that, despite its size, WellCare
will not be as competitive as Aetna
because Aetna’s overall health
insurance business was larger than that
of WellCare.14 Before the divestiture,
however, WellCare already competed
successfully as a smaller competitor
than Aetna. From 2018 to 2019,
WellCare organically grew its business
by over 40 percent, from approximately
1 million members to over 1.4 million
members.15 More importantly, with the
acquisition of Aetna’s individual PDP
business, WellCare’s total individual
13 See,
e.g., TC-003, TC-024, and TC-060.
e.g., TC-003, TC-024.
15 See CMS Monthly Enrollment by CPSC for
January 2019, available at https://www.cms.gov/
Research-Statistics-Data-and-Systems/StatisticsTrends-and-Reports/MCRAdvPartDEnrolData/
Monthly-Enrollment-by-Contract-Plan-StateCounty-Items/Monthly-Enrollment-by-CPSC-201901.html?DLPage=1&DLEntries=10&DLSort=
1&DLSortDir=descending.
14 See,
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PDP membership is well over three
million members, approximately 50
percent more than Aetna’s predivestiture individual PDP membership.
Following the divestiture, WellCare will
be well-positioned to achieve any
benefits of scale that Aetna had enjoyed
in its individual PDP business, enabling
it to be an even more formidable
competitor than it previously was and
ensuring that the remedy is well within
the ‘‘reaches of the public interest,’’ as
required under the Tunney Act. See
Microsoft, 56 F.3d at 1461.
Concerns that WellCare is not getting
enough assets or a stand-alone business
unit from Aetna misunderstand the
context of the remedy here.16 The
Antitrust Division’s experience, as
reflected in the 2004 Policy Guide to
Merger Remedies,17 is that in some
instances, an in-market buyer does not
need a stand-alone business unit to be
successful: ‘‘The Division will approve
the divestiture of less than an existing
business entity if the evidence clearly
demonstrates that certain of the entity’s
assets already are in the possession of,
or readily obtainable in a competitive
market by, the potential purchaser.’’18
Consistent with this principle, the
proposed Final Judgment ensures that
WellCare will have all that it needs to
preserve competition in the sale of
individual PDPs. WellCare has
purchased Aetna’s entire individual
PDP business throughout the United
States, including the relevant contracts,
the right to hire employees, and access
to all relevant data. Focusing on a standalone ‘‘business unit’’ in this case
ignores the critical fact that WellCare
already offers individual PDPs
throughout the United States, is
licensed in all 50 states, and has
scalable in-house capabilities that it
does not need to duplicate. These
capabilities include experience
competing in individual PDP markets
throughout the country, actuarial
expertise, as well as clinical and
administrative resources. Because of
these existing capabilities, WellCare
does not need to acquire a stand-alone
business unit to compete for the sale of
individual PDPs. Instead, WellCare is
16 See,
e.g., TC-024, TC-060.
is the operative guide on remedies
following the September 25, 2018 withdrawal of the
2011 Policy Guide to Merger Remedies. See Makan
Delrahim, It Takes Two: Modernizing the Merger
Review Process, Remarks at the 2018 Global
Antitrust Enforcement Symposium (September 25,
2018), available at https://www.justice.gov/opa/
speech/assistant-attorney-general-makan-delrahimdelivers-remarks-2018-global-antitrust.
18 Antitrust Division Policy Guide to Merger
Remedies, October 2004, at 14, available at https://
www.justice.gov/sites/default/files/atr/legacy/2011/
06/16/205108.pdf.
17 This
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acquiring key competitive assets that
complement its existing capabilities and
allow WellCare to step quickly and
effectively into Aetna’s shoes as a
significant competitor for the sale of
individual PDPs.
Despite WellCare’s in-market
expertise, the joint comments by
Consumer Action and U.S. PIRG 19 and
PUTT and PSSNY 20 erroneously argue
that WellCare is similarly situated to
Molina, the proposed divestiture buyer
of Aetna’s Medicare Advantage business
that Judge Bates rejected in an opinion
enjoining Aetna’s proposed acquisition
of Humana.21 This concern fails to
appreciate that WellCare is differently
situated than Molina in several ways.
Unlike Molina, which had ‘‘made forays
into the individual Medicare Advantage
market’’ but never succeeded,22
WellCare has consistently maintained a
presence in the individual PDP business
since the program’s inception in 2006.
Also, Aetna proposed to divest only
small portions of each of the merging
parties’ Medicare Advantage business to
Molina. In contrast, while WellCare has
not purchased a stand-alone business
unit, it has purchased Aetna’s entire
individual PDP business, including
Aetna’s business outside the affected
geographic markets. Medicare
Advantage products also differ
significantly from individual PDP
products. In addition to the pharmacy
networks used by PDPs, Medicare
Advantage products require a
comprehensive network of hospitals,
doctors, and other healthcare providers
at competitive rates. In Aetna/Humana,
Molina had no presence at all in 89
percent of the counties referenced in the
United States’ complaint and no
Medicare presence in 95 percent of the
counties, so the company would have
needed to build its own provider
network to compete in the market.23 By
contrast, WellCare already has an
extensive pharmacy network that it uses
to sell individual PDPs throughout the
United States and will not have to
assemble any new networks in any
region to offer individual PDPs. Thus,
unlike Molina in Aetna/Humana,
WellCare is both purchasing an entire
business and is a qualified buyer with
the assets and capabilities to continue
competing successfully.
19 TC-023
at 3–4, TC-024 at 5–6.
at 21.
21 United States v. Aetna, Inc., 240 F. Supp. 3d
1, 73 (D.D.C. 2017).
22 Id. at 62.
23 Id. at 65.
20 TC-060
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2. WellCare is an independent
competitor to CVS.
Although some commenters raised
concerns that WellCare will not operate
independently of CVS because WellCare
uses Caremark (which CVS owns) as its
PBM,24 the United States carefully
considered this relationship in
evaluating WellCare’s suitability as the
divestiture buyer and ultimately
concluded that WellCare will continue
to be an independent competitor to CVS
for several reasons.
First, CVS has no governance control
over WellCare. Rather, WellCare is a
separate corporate entity with an
independent board of directors. Second,
CVS and WellCare do not have common
financial incentives. As a separate
company, WellCare is driven to focus on
its own business and compete
vigorously against CVS. Third, while
WellCare may make the independent
business decision to use Caremark
rather than its other PBM options,
nothing in the proposed Final Judgment
requires WellCare to do so. In fact,
WellCare recently announced that it is
putting its PBM services contract out to
bid in the summer of 2019.25 Fourth,
WellCare recently acquired a small PBM
called Meridian, which improves
WellCare’s ability to provide its own
PBM services. Finally, Caremark’s
business has internal firewalls designed
to prevent insurance customers’
information from being shared with
SilverScript and other insurance
customers. This means that WellCare,
like all of Caremark’s health plan
customers, can make its own
independent business decisions with
the protections these firewalls provide
against the risk that SilverScript, or any
other Caremark customer, will have
access to competitively sensitive
information or advance knowledge of its
business plans and other competitive
decisions.
Because WellCare retains control of
the divestiture assets and has the
financial incentive to use them in its
best interests, rather than CVS’s,
WellCare’s relationship with Caremark
does not change the conclusion that the
proposed remedy is in the public
interest. This conclusion is bolstered by
the success of Aetna’s individual PDP
plans, which used Caremark for PBM
services before the merger, showing that
a relationship with Caremark does not
24 See, e.g., TC-003, TC-015, TC-060, TC-061, and
TC-080.
25 See ‘‘WellCare Fourth Quarter 2018 Earnings
Conference Call Transcript’’ (February 5, 2019)
available at https://www.fool.com/earnings/calltranscripts/2019/02/05/wellcare-health-plans-incwcg-q4-2018-earnings-con.aspx (last visited
February 13, 2019).
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impede an individual PDP’s
competitiveness. Similarly, WellCare
has also competed against CVS’s
SilverScript business for many years
despite using Caremark for PBM
services.
Other comments incorrectly suggest
that, because the proposed Final
Judgment includes transition services
agreements for 2019, WellCare will not
operate the divestiture assets
independently of CVS.26 As described
above, the proposed Final Judgment
requires that, at WellCare’s option, CVS
must enter into an administrative
services agreement to provide WellCare
with all of the services required to
manage the divestiture assets through
the 2019 plan year. CVS must offer these
services at the direction of WellCare and
subject to the review of both the
monitoring trustee and the United
States, whose oversight will likely deter
any attempts to undermine WellCare’s
competitiveness.
The transition services agreements are
also only in place through 2019. This
temporary arrangement provides
continuity to members who purchased
an Aetna individual PDP during the
open-enrollment period that ran from
October through December 2018, but
ends when plans for 2020 will become
effective. These transition services are
necessary for the seamless and efficient
transition of Aetna’s individual PDP
business to WellCare. Importantly, the
agreements do not affect the prices,
design, coverage amounts, and other
terms of the plans WellCare is now
offering to seniors. Rather, these terms
have been fixed for all of 2019.
Further, the monitoring trustee is
closely tracking CVS’s compliance with
the terms of the transition services
agreements. CVS’s obligations are
clearly stated in the proposed Final
Judgment, and the monitoring trustee is
already ensuring that CVS is fulfilling
its responsibilities. Because Aetna’s
contracts with CMS, as well as the
related data, have been transferred in
accordance with the terms of the
proposed Final Judgment, WellCare has
all the assets it needs to independently
prepare for the next competitive event—
the June 2019 submission of the bid for
2020—which is not impacted by the
transition services agreements.
3. Prior health insurance merger
remedies do not cast doubt on the
divestiture.
In 2012, the United States required
Humana Inc. and Arcadian Management
Services Inc. to divest assets relating to
Arcadian’s Medicare Advantage
26 TC-003,
PO 00000
TC-023, and TC-024.
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business in 51 counties in five states in
order for Humana to proceed with an
acquisition of Arcadian.27 Several
commenters looked at this and other
divestitures in hindsight and conclude
that they failed or that divestitures in
general are not successful remedies.28
As a general matter, however, the
factual circumstances in every
divestiture are different. Furthermore,
the concerns that the experience of prior
divestitures indicates that the
divestiture to WellCare will fail in this
instance are wrong because the
circumstances here are different.
Indeed, there are several key
differences between this divestiture and
the ones in Humana/Arcadian, the most
important of which is the scope of the
divestiture. In Humana/Arcadian the
divestiture did not constitute an entire
business, as it included only 12,700
covered lives in 51 rural counties and
was split between three different
acquirers. In contrast, CVS has divested
Aetna’s entire individual PDP business,
consisting of over two million members
and including assets outside the markets
described in the Complaint.
Additionally, similar to Molina in
Aetna/Humana, the Humana/Arcadian
divestitures concerned Medicare
Advantage products and some of those
divestitures went to buyers that did not
have Medicare Advantage provider
networks in the divested markets. In
contrast, WellCare already has
pharmacy networks in every region of
the United States. Divesting the entire
line of business to WellCare, a wellpositioned buyer, will help ensure that
WellCare continues to compete
effectively and capture additional
economies of scale across its entire
business.
Despite these factual differences,
commenters also note that WellCare was
the buyer of one set of divested assets
in Humana/Arcadian and wrongly
suggest that, because that divestiture
failed, this one likely will too.29 As
described above, the two divestitures
are substantially different. In Humana/
Arcadian, WellCare acquired fewer than
5,000 lives in two counties in Arizona.
In contrast, WellCare is acquiring over
2.1 million individual PDP lives across
the United States from Aetna.
Additionally, as described above,
27 See ‘‘Justice Department Requires Divestitures
in Humana Inc.’s Acquisition of Arcadian
Management Services Inc.,’’ available at https://
www.justice.gov/opa/pr/justice-departmentrequires-divestitures-humana-incs-acquisitionarcadian-management-services.
28 TC-003, TC-023, TC-024, and TC-060.
29 TC-023, TC-024, and TC-060; see also Amicus
Brief from the AIDS Healthcare Foundation, Dkt. #
50-1.
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WellCare did not have a Medicare
Advantage provider network in Arizona
before the divestiture in Humana/
Arcadian while WellCare already has an
established pharmacy network in place
that it can use for the PDP business it
is acquiring from Aetna. Further,
WellCare has grown significantly as a
company since 2012—more than
doubling from 2.7 million 30 members to
5.5 million 31—and overhauled its
leadership team, including the CEO,
CFO, CIO, CMO, and the EVP for
Clinical Operations.32 Because of the
larger scale of the current divestiture,
WellCare’s growth as a health insurance
company, and its experience and
existing capabilities with individual
PDPs, WellCare’s performance with the
Humana/Arcadian assets does not
indicate how successful it will be with
Aetna’s PDP business. Because a district
court ‘‘must accord deference to the
government’s predictions about the
efficacy of its remedies,’’ SBC
Commc’ns, 489 F. Supp. 2d at 17, and
because the divestiture to WellCare is
readily distinguishable from the ones
that commenters allege failed in
Humana/Arcadian, the Court should
afford deference to the government’s
prediction of a successful divestiture in
this instance.
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4. The remedy does not create new
structural concerns in the markets for
individual PDPs.
The AMA incorrectly argues that,
because WellCare and Aetna both
compete in all 34 Medicare regions, the
divestiture itself creates competitive
concerns simply by reducing the
number of competitors in every
region.33 The AMA further alleges that,
in seven regions, the divestiture ‘‘would
potentially raise significant competitive
concerns [that] often warrant scrutiny’’
because it exceeds certain Herfindahl–
Hirschman Index (‘‘HHI’’) thresholds in
the Horizontal Merger Guidelines.34
HHIs are a commonly accepted
measure of market concentration and
are calculated by squaring the market
share of each firm competing in the
market and then summing the resulting
numbers.35 The U.S. Department of
30 See ‘‘WellCare 2011 Annual Report’’, available
at https://ir.wellcare.com/file/4091918/Index?Key
File=1500074253.
31 See ‘‘WellCare Corporate Overview’’, available
at https://www.wellcare.com/en/Corporate/
Company-Overview (last visited February 13, 2019).
32 See ‘‘WellCare Corporate Management Team’’,
available at https://www.wellcare.com/Corporate/
Management-Team (last visited February 13, 2019).
33 TC-030 at 6-7.
34 Id.
35 For example, for a market consisting of four
firms with shares of 30, 30, 20, and 20 percent, the
HHI is 2,600 (302 + 302 + 202 + 202 = 2,600).
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Justice, consistent with the Federal
Trade Commission, generally considers
markets in which the HHI is between
1,500 and 2,500 points to be moderately
concentrated, and considers markets in
which the HHI is in excess of 2,500
points to be highly concentrated.36
Transactions that increase the HHI by
more than 100 points in moderately
concentrated markets or between 100
and 200 points in highly concentrated
markets ‘‘potentially raise significant
competitive concerns and often warrant
scrutiny.’’ 37 Transactions that increase
the HHI by more than 200 points in
highly concentrated markets are
‘‘presumed to be likely to enhance
market power.’’ 38
In this case, although some regions
fall into the category of ‘‘potentially’’
raising concerns under the Horizontal
Merger Guidelines after the divestiture,
no regions are above the threshold for
‘‘presumed’’ concerns. Moreover, as
described in the 2010 Horizontal Merger
Guidelines, while the United States
does use HHIs and other concentration
statistics, such as the number of firms in
the market, as an important part of its
investigative toolkit, ‘‘[t]he purpose of
these thresholds is not to provide a rigid
screen to separate competitively benign
mergers from anticompetitive ones . . .
[r]ather, they provide one way to
identify some mergers unlikely to raise
competitive concerns and some others
for which it is particularly important to
examine whether other competitive
factors confirm, reinforce, or counteract
the potentially harmful effects of
increased concentration.’’ 39 Consistent
with these principles, the United States
considered the strength of WellCare,
Aetna, and their competitors in all 34
PDP regions. The combined market
share of Aetna’s and WellCare’s
individual PDP businesses does not
exceed 25 percent in any region. The
United States determined that the
combination of Aetna’s and WellCare’s
PDP business was not likely to
substantially lessen competition, in part
due to the presence of other significant
competitors—including CVS’s
SilverScript product—in every market.
5. The licensing provisions related to
the Aetna brand protect WellCare’s
ability to compete using the divested
assets.
Under Section IV.I. of the proposed
Final Judgment, Aetna is required to
36 See U.S. Department of Justice & FTC,
Horizontal Merger Guidelines § 5.3 (2010),
available at https://www.justice.gov/atr/file/
810276/download.
37 Id.
38 Id.
39 Id.
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license the Aetna brand to WellCare for
use with the divested business only for
2019. For 2020, Section IV.J. of the
proposed Final Judgment prohibits CVS
from using the Aetna brand for the sale
of individual PDPs. Misunderstanding
these provisions, the joint comment
from Consumer Action and U.S. PIRG
raises concerns that WellCare’s one-year
license to the Aetna brand fails to create
an incentive to properly invest in the
Aetna brand name.40 The proposed
Final Judgment, however, is not meant
to give WellCare a long-term incentive
to invest in the Aetna brand name.
Rather, these provisions give WellCare a
two-year opportunity to establish its
relationship with the customers of the
divested plans without a competing
Aetna-branded individual PDP plan.
Given that, as previously explained, the
divestiture improves WellCare’s
established ability to compete for PDP
customers, these provisions further
enhance the effectiveness of the
proposed Final Judgment.
6. The sales price does not cast doubt
on WellCare’s intention to compete.
Several commenters raise misplaced
concerns related to the price paid by
WellCare.41 For example, the joint
comment from Consumer Action and
U.S. PIRG estimates the divestiture
purchase price to be $45 per life and
then claims—without evidence—that
this ‘‘seems like a very cheap price.’’ 42
In some cases, a low purchase price may
raise concerns whether a proposed
divestiture buyer will be a successful
competitor.43 As described in the 2004
Policy Guide to Merger Remedies, ‘‘the
purchase price will not be approved if
it clearly indicates that the purchaser is
unable or unwilling to compete in the
relevant market.’’ 44 The Policy Guide
also states, however, that ‘‘a successful
divestiture does not depend on the price
paid for the assets.’’ 45 Rather, a low
price ‘‘may simply mean the purchaser
is getting a bargain’’ and ‘‘if the Division
has other sufficient assurances that the
proposed purchaser intends to compete
in the relevant market, the Division will
not require . . . [a certain] price.’’ 46
40 TC-023,
TC-024; see also TC-003.
TC-023, TC-024, and TC-060.
42 TC-023 at 5, TC-024 at 7.
43 See, e.g., United States v. Aetna, Inc., 240 F.
Supp. 3d 1, 72 (D.D.C. 2017) (citing to an
‘‘extremely low’’ purchase price as evidence that
the divestiture buyer was not likely to be able to
replace the competition lost by the merger).
44 Antitrust Division Policy Guide to Merger
Remedies, October 2004, at 33 available at https://
www.justice.gov/sites/default/files/atr/legacy/2011/
06/16/205108.pdf.
45 Id.
46 Id. at 34.
41 TC-003,
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In this case, the Antitrust Division has
those assurances. The United States
thoroughly vetted WellCare, which has
offered individual PDPs since the
program’s inception in 2006 and has
recently experienced strong organic
growth.47 The United States interviewed
WellCare’s executives, reviewed its
business plans, and discussed WellCare
with relevant third parties. Based on
these efforts, the United States believes
that WellCare will continue to compete
in individual PDPs, a market it has
participated in for over a decade. The
commenters do not provide any
evidence that their estimated purchase
price undermines this conclusion.
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B. Comments Related to the Vertical
Aspects of CVS’s Acquisition of Aetna
Asking the Court to go outside the
permissible scope of review under the
Tunney Act, commenters also raise
vertical concerns about the merger
combining CVS’s pharmacy and PBM
businesses with Aetna’s health
insurance businesses, alleging that the
merger will enable CVS to use its assets
to harm competitors. CVS can be viewed
as competing at three different levels of
the healthcare industry: (1) the sale of
drugs through channels such as retail,
mail order, and long-term care
pharmacies; (2) the provision of PBM
services that are offered to insurers,
including the negotiation of rates with
pharmaceutical manufacturers and the
negotiation of coverage networks with
pharmacies; and (3) the sale of various
types of insurance, including individual
PDPs. CVS competes at all three of these
levels through its branded retail, longterm care, and other pharmacies;
through its PBM, Caremark; and through
SilverScript, its individual PDP. Aetna
competes with SilverScript at the third
level, and offers additional types of
insurance, but does not offer standalone PBM services or own any retail
pharmacies of its own.
Recognizing that CVS and Aetna do
not compete against each other either at
the retail pharmacy level or the PBM
level, commenters nonetheless raise two
categories of vertical concerns relating
to the merger: input foreclosure and
customer foreclosure concerns, which
are explained below. Commenters also
raise vertical concerns about CVS’s
common ownership of its retail
pharmacies and Caremark, its PBM,
47 See CMS Monthly Enrollment by CPSC for
January 2019, available at https://www.cms.gov/
Research-Statistics-Data-and-Systems/StatisticsTrends-and-Reports/MCRAdvPartDEnrolData/
Monthly-Enrollment-by-Contract-Plan-StateCounty-Items/Monthly-Enrollment-by-CPSC-201901.html?DLPage=1&DLEntries=10&DLSort=
1&DLSortDir=descending.
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which CVS owned long before it sought
to acquire Aetna and is unrelated to the
current merger.
The United States investigated the
potential for vertical harms from the
merger by obtaining and reviewing
documents as well as interviewing
industry participants. For the reasons
outlined below, the United States
concluded that vertical harms were
unlikely to occur and did not allege any
harm related to vertical concerns in its
Complaint. The vertical concerns
therefore are outside the scope of this
Tunney Act proceeding. See United
States’ December 14, 2018 Response to
Order to Show Cause, Dkt. #32, at 3–7.
Responding to the AAI’s comment that
there are benefits to transparency, the
United States nonetheless describes the
commenters’ concerns and responds
below.
1. Input foreclosure is unlikely to occur
and is beyond the scope of the
Complaint.
Although several comments raise the
possibility that the merged firm will
harm competition in the sale of health
insurance by raising the cost of
important services or products that CVS
provides to insurers that compete with
Aetna, which is known as input
foreclosure, the United States
considered this possibility and
determined that input foreclosure is
unlikely to be profitable for CVS. In
particular, commenters argue that CVS
will deny or restrict health insurance
rivals’ access to inputs at two different
levels of the supply chain: First,
commenters 48 allege that the company
will not make its pharmacies available
to competing health plans or will
otherwise disadvantage rival plans by
raising pharmacy costs. Second,
commenters 49 allege that Caremark will
not make its PBM services available to
competing health plans or will raise the
prices for its PBM services to rival
plans.50 Neither is likely to occur.
48 TC-001, TC-002, TC-003, TC-023, and TC-024;
see also Amicus Brief from the AIDS Healthcare
Foundation, Dkt. # 50-1.
49 TC-001, TC-002, TC-003, TC-023, TC-024, TC048, TC-054, and TC-057.
50 Additionally, some commenters also allege that
CVS is foreclosing 340B administrators from its
retail pharmacies. See TC-066, TC-068. 340B
administrators offer services to assemble and
administer pharmacy networks that provide rebates
to qualified hospitals. CVS competes with these
administrators through a subsidiary called
Wellpartner. These commenters allege that CVS
does not allow its pharmacies to participate in 340B
networks unless Wellpartner is selected as the
hospital’s 340B administrator, which would be a
form of input foreclosure. CVS’s acquisition of
Aetna does not relate to the 340B market or affect
shares in that market. In part for this reason, the
United States did not allege anticompetitive effects
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As noted in a set of questions and
answers issued on the same day the
Complaint and proposed Final
Judgment were filed, the United States
carefully considered these issues as part
of its investigation.51 The evidence
showed that CVS is unlikely to be able
to profitably raise its PBM or retail
pharmacy costs post-merger. If CVS
were to raise prices at any level of the
supply chain, it would lose customers to
competing PBMs or retail pharmacies,
and the merged entity likely would not
be able to offset these losses by
capturing additional health insurance
customers. For these reasons, the United
States did not allege input foreclosure in
its Complaint, making this issue beyond
the scope of this Tunney Act
proceeding.
Despite the evidence, the AMA also
argues that the divestiture will fail
because WellCare will be foreclosed
from pharmacy and PBM services.52 In
effect, this argument asserts that the
input foreclosure described above will
occur and will be directed at WellCare.
As discussed above, the United States
concluded that such foreclosure—
whether directed at WellCare or any
other insurer—is unlikely to occur.
Furthermore, even before the
divestiture, WellCare (and Aetna)
competed successfully against CVS’s
SilverScript PDP business despite the
vertical relationship between
SilverScript and Caremark. With the
divestiture, CVS’s share of the
individual PDP market will not grow, so
the merger will not increase CVS’s
incentive or ability to foreclose its PDP
rivals—including WellCare—from CVS
pharmacies or Caremark.
2. Customer foreclosure is unlikely to
occur and is beyond the scope of the
Complaint.
Other comments allege that the
merged firm would harm pharmacies by
denying them access to Aetna members,
even though the merger does not
significantly increase CVS’s incentive to
engage in this behavior, which is known
as ‘‘customer foreclosure.’’ 53
Commenters—primarily independent
pharmacies that compete with CVS—
allege that Caremark favors CVS
from the merger related to CVS or Wellpartner’s
practices, placing the concerns of these commenters
outside of the Court’s Tunney Act review. See Dkt.
#32, at 3–7.
51 See ‘‘United States v. CVS and Aetna Questions
and Answers for the General Public,’’ available at
https://www.justice.gov/opa/press-release/file/
1099806/download.
52 TC-003 at 12.
53 TC-002, TC-023, TC-024, TC-035, TC-048, TC059, TC-060, TC-070, TC-076, TC-078; see also
Amicus Brief from the AIDS Healthcare
Foundation, Dkt. # 50-1.
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pharmacies in its reimbursements.54
The commenters allege that this
favoritism can be observed in Caremark
programs such as mandatory mail order,
which steers customers away from
independent pharmacies.55 Commenters
also allege that Caremark manipulates
reimbursement to independent
pharmacies, sometimes later offering to
buy them and turn them into CVS
stores,56 and that several states are
investigating these practices.57 From
these allegations, these commenters
incorrectly conclude that CVS is likely
to use Aetna to steer additional
customers away from rival pharmacies,
causing them harm.
The United States takes these
allegations seriously and considered
them during its investigation. Generally,
the United States considers the merging
companies’ prior acts when evaluating
the likely effects of a transaction, but
mergers are illegal under the Clayton
Act only if they will likely substantially
lessen competition in a relevant
market.58 Based on its investigation, the
United States determined that CVS’s
acquisition of Aetna likely would not
result in an anticompetitive customer
foreclosure strategy, particularly given
Aetna’s small share in many commercial
health insurance markets. The
combination of Aetna’s small share of
retail pharmacy purchases in many
areas, competition from rival insurers
who would win additional sales if
Aetna provided a less desirable
pharmacy network, and other factors
make it unlikely that this strategy would
be profitable for CVS. Therefore, the
United States did not allege customer
foreclosure in its Complaint, placing
this issue beyond the scope of this
Tunney Act proceeding. See Dkt. #32, at
3–7. Consequently, these comments do
not provide a basis for rejecting the
proposed Final Judgment. See U.S.
Airways, 38 F. Supp. 3d at 76
(‘‘ ‘Moreover, the Court’s role under the
APPA is limited to reviewing the
remedy in relationship to the violations
that the United States has alleged in its
Complaint. . . .’ ’’) (quoting United
54 TC-001, TC-002, TC-004 TC-012, TC-013, TC016, TC-017, TC-021, TC-023, TC-024, TC-027, TC031, TC-032, TC-033, TC-034, TC-039, TC-043, TC044, TC-045, TC-050, TC-059, TC-060, TC-065, TC075, TC-076, TC-080, TC-083, TC-085.
55 TC-001, TC-002, TC-016, TC-020, TC-021, TC027, TC-035, TC-039, TC-045, TC-046, TC-054, TC059, TC-061, TC-062, TC-074, TC-080, TC-081.
56 TC-004, TC-013, TC-017, TC-023, TC-024, TC025, TC-031, TC-032, TC-033, TC-038, TC-039, TC046, TC-061, TC-064, TC-074; see also Amicus Brief
from the AIDS Healthcare Foundation, Dkt. # 50-1.
57 TC-016, TC-031, TC-044, TC-054, TC-059, TC060, TC-061, TC-063, TC-064, TC-072, TC-078, TC080, TC-081, TC-082, TC-083; see also Amicus Brief
from the AIDS Healthcare Foundation, Dkt. # 50-1.
58 See 15 U.S.C. § 18.
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States v. Graftech Int’l Ltd., No. 1:10CV-02039-RMC, 2011 WL 1566781, at
*13 (D.D.C. Mar. 24, 2011)).
3. Vertical concerns are not addressable
under the Tunney Act’s standard of
review.
Although their comments are outside
the scope of the Court’s Tunney Act
review because the Complaint does not
allege vertical harms, some commenters
weighed in on the standard of review
under the Tunney Act 59 or commented
that the Court may still consider vertical
concerns if the Complaint is drafted so
narrowly as to make a ‘‘mockery of
judicial power,’’ an argument that is
unsupported by the caselaw, as
discussed above.60 Indeed, as the D.C.
Circuit recognized in Microsoft, 56 F.3d
at 1459, a district court may not
evaluate the scope of the complaint
during a Tunney Act review, even if the
court believes that additional claims
would have been justified. While a court
is not obliged to accept a consent decree
that ‘‘makes a mockery of judicial
power,’’ id. at 1462, under Microsoft
that standard applies to the consent
decree—not the complaint—and
subsequent cases suggesting otherwise
are inconsistent with Microsoft.
In any event, neither the Complaint
nor the proposed Final Judgment is
drafted so narrowly as to make a
mockery of judicial power. To the
contrary, the Complaint is significant in
scope: it challenges anticompetitive
harm in 16 broad regions, encompassing
22 states, affecting millions of seniors.
The proposed Final Judgment goes even
further, addressing the anticompetitive
harm with the nationwide divestiture of
Aetna’s entire individual PDP business.
Furthermore, the fact that the
divestiture represents a small fraction of
the underlying $69 billion merger is not
relevant to the public-interest
determination and is not a basis for
concluding that the proposed remedy
makes a mockery of the judicial process,
as some commenters suggest.61 Courts
have routinely found proposed
judgments to be in the public interest
when the United States challenged only
a small part of a large transaction,62 and
59 TC-001, TC-002, TC-003, TC-023, TC-024, TC060; see also Amicus Brief from the AIDS
Healthcare Foundation, Dkt. # 50-1.
60 TC-001, TC-002, TC-023, TC-024, TC-059, and
TC-060; see also Amicus Brief from the AIDS
Healthcare Foundation, Dkt. # 50-1.
61 TC-001; see also Amicus Brief from the AIDS
Healthcare Foundation, Dkt. # 50-1.
62 See United States v. Parker-Hannifin Corp. and
CLARCOR Inc., 1:17-cv-01354 (D. Del. Sept. 26,
2017) (complaint alleging harm in only two product
markets, which resulted in a divestiture of a
business with annual revenues of approximately
$60 million, in challenge to $4.3 billion
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5475
settlements are often ideal in these
situations because they allow parties to
proceed with transactions that could
otherwise benefit consumers. Because
Aetna was the nation’s third-largest
health insurance company, it is not
surprising that its individual PDP
business, while substantial, represents
only a small percentage of the
company’s total value. The United
States made these arguments in more
detail in its December 14, 2018
Response to Order to Show Cause, see
Dkt. #32, and incorporates that pleading
herein by reference.
C. Other Miscellaneous Comments
Even though CVS and Aetna
significantly compete against each other
only in the sale of individual PDPs,
several commenters raised irrelevant
concerns related to other markets,
including whether the merger will
increase entry barriers in either the PBM
or health insurance markets,63 or reduce
PBM competition by eliminating Aetna
as a potential entrant in the PBM
market.64 During its investigation, the
United States seriously considered
whether the merger likely would harm
competition in the PBM and health
insurance markets, including by
increasing entry barriers and
eliminating Aetna as a PBM competitor.
Among other things, the United States
obtained and reviewed documents and
interviewed industry participants about
these issues. In reviewing such
information, the United States
determined that the evidence did not
show that the merger likely would harm
competition in these areas. Accordingly,
the Complaint did not allege that CVS’s
acquisition of Aetna would harm
competition in PBM and health
insurance markets other than the sale of
individual PDP plans. These comments
are thus beyond the purview of the
Tunney Act and do not provide a basis
for rejecting the proposed Final
Judgment. See U.S. Airways, 38 F. Supp.
3d at 76 (‘‘[T]he Court’s role under the
APPA is limited to reviewing the
remedy in relationship to the violations
transaction); United States v. United Technologies
Corp. and Goodrich Corp., 1:12-cv-01230 (D.D.C.
July 26, 2012) (complaint alleging harm in only two
product markets, resulting in a divestiture of
businesses expected to generate approximately $395
million in annual revenues, in challenge to $18.4
billion transaction); United States v. InBev N.V./
S.A. et al., 1:08-cv-01965 (D.D.C. Nov. 14, 2008)
(complaint alleging harm in only three regions of
upstate New York in challenge to InBev’s proposed
acquisition of Anheuser-Busch for approximately
$52 billion).
63 TC-002, TC-003.
64 TC-001, TC-003; see also Amicus Brief from the
AIDS Healthcare Foundation, Dkt. # 50-1.
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that the United States has alleged in its
Complaint.’’) (internal citation omitted).
Although some commenters
expressed concern about concentration
in the PBM market, these concerns are
misplaced because Aetna does not
provide stand-alone PBM services.
These commenters state that only three
companies—Caremark, ESI, and
Optum—control over 80% of the PBM
marketplace 65 and are simply too
powerful,66 with the ability to harm
pharmacies, including by forcing ‘‘take
it or leave it’’ contracts on independent
pharmacies. The commenters also
complain about PBM business practices,
such as ‘‘spread pricing’’ on
pharmaceuticals, which the commenters
allege limits transparency and harms
independent pharmacies.67
Additionally, the AMA and other
commenters raised concerns that the
vertically integrated PBM/health
insurers (Cigna–Express Scripts, Optum
Rx–United Healthcare, and CVS–Aetna)
would have increased incentives
following the merger to coordinate by
bidding less aggressively for PBM
contracts that would strengthen their
health insurer rivals or that the large
vertically integrated PBM/health
insurers would have stronger incentives
to prevent market entry by other PBMs
or the introduction of innovative drug
business models.68 The merger,
however, does not significantly increase
concentration in the PBM market
because Aetna does not offer standalone PBM services. Also, these
comments do not relate to whether the
proposed Final Judgment reasonably
addresses the harms alleged in the
Complaint. Therefore, they are well
beyond the scope of this Tunney Act
proceeding and do not provide a basis
for rejecting the proposed Final
Judgment. See U.S. Airways, 38 F. Supp.
3d at 76 (‘‘[T]he Court’s role under the
APPA is limited to reviewing the
remedy in relationship to the violations
that the United States has alleged in its
Complaint.’’) (internal citation omitted).
Some commenters raised concerns
about the effectiveness of firewalls at
65 TC-002, TC-004, TC-009, TC-015, TC-020, TC023, TC-024, TC-026, TC-029, TC-038, TC-044, TC046, TC-054, TC-056,TC-059, TC-060, TC-061, TC080, TC-083; see also Amicus Brief from the AIDS
Healthcare Foundation, Dkt. # 50-1.
66 TC-014, TC-023, TC-024, TC-026, TC-027, TC037, TC-044, TC-046, TC-054, TC-056, TC-057, TC059, TC-062.
67 TC-009, TC-014, TC-015, TC-016, TC-017, TC020, TC-021, TC-023, TC-024, TC-025, TC-031, TC033, TC-044, TC-045, TC-047, TC-056, TC-059, TC060, TC-061, TC-062, TC-063, TC-064, TC-072, TC074, TC-078, TC-080, TC-081, TC-082, TC-085; see
also Amicus Brief from the AIDS Healthcare
Foundation, Dkt. # 50-1.
68 TC-002, TC-003.
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Caremark, despite CVS’s commercial
incentive to maintain those firewalls.
The AAI expressed concerns that
ineffective firewalls would allow
Caremark to facilitate coordination
among health insurers that use it as a
PBM.69 The United States investigated
this possibility and determined that
CVS is commercially incentivized to
maintain firewalls because that
customers could switch to an alternative
PBM if their information were not kept
confidential. MSSNY raised a related
concern regarding the potential for
consumer data breaches due to data
being shared between the merged
entities, but CVS already handles
sensitive consumer data from
Caremark’s PBM business. Nothing
about the merger changes CVS’s
incentive or ability to protect this
information.
Other commenters applied the wrong
legal standard when they argued that
the Court should reject the settlement
because consumers may not benefit
from the merger of CVS and Aetna. The
AAI and the joint comment from
Consumer Action and U.S. PIRG 70
argue that there is little evidence that
past vertical mergers have benefitted
consumers, and several commenters 71
suggested that there is no evidence that
cost savings will be passed through to
customers. Mergers, however, are illegal
under the Clayton Act only if they
substantially lessen competition in a
relevant product market, not if they fail
to pass on benefits to consumers in
markets where competition likely will
not be substantially lessened.72
Consequently, these comments do not
provide a basis for rejecting the
proposed Final Judgment.
Some commenters raised other
concerns that are beyond the scope of
the Complaint in this case. For example,
several commenters, including the
MSSNY, said that the merger would
harm physicians and other healthcare
providers in a number of ways,
including through steering patients
away from physician groups or by
imposing administrative burdens on
physicians.73 They also argue that these
actions would harm patients. Without
relating their concerns to the merger,
other commenters allege that the
69 See
also TC-045.
TC-023, and TC-024.
71 TC-003, TC-023, TC-024, TC-054, TC-059.
72 See 15 U.S.C. § 18.
73 TC-001, TC-004, TC-007, TC-011, TC-029, TC048, TC-060, TC-067, TC-070, TC-078, TC-081; see
also Amicus Brief from the AIDS Healthcare
Foundation, Dkt. # 50-1. MSSNY further argued that
these practices would be driven by the $40 billion
in debt that CVS is incurring as part of the
transaction.
70 TC-002,
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pharmacy 74 or insurance 75 markets are
concentrated, raise concerns relating to
CVS’s existing pricing practices,76 note
that CVS is involved in an ongoing
federal whistleblower case,77 or
complain about CVS’s long-term care
pharmacy.78 As these comments do not
relate to whether the proposed Final
Judgment reasonably addresses the
harms alleged in the Complaint, they are
well beyond the scope of this Tunney
Act proceeding and do not provide a
basis for rejecting the proposed Final
Judgment. See U.S. Airways, 38 F. Supp.
3d at 76 (‘‘[T]he Court’s role under the
APPA is limited to reviewing the
remedy in relationship to the violations
that the United States has alleged in its
Complaint.’’) (internal citation omitted).
D. Comments in Support of the Merger
Twenty-six commenters expressed
support for the merger or praised CVS’s
business practices.79 Commenters,
including the California Asian Pacific
Chamber of Commerce, Connecticut
Business and Industry Association,
Atlanta Children’s Shelter, SISU
Integrated Early Leaning, and API
Council, discussed the merger’s
potential to create an innovative
platform that will improve access to
high quality and affordable healthcare.
In particular, the Asian Business
Association and the API Council
discussed the potential of the merger to
allow for more collaboration between
doctors, pharmacists, and insurers,
resulting in improved patient care.
Commenters, including the Spanish
Speaking Elderly Council-RAICES, Inc.,
the Latino Commission on AIDS,
National Hispanic Medical Association,
and the National Black Nurses
Association, praised CVS for improving
public health through removing tobacco
from its stores, participating in
programs to combat the opioid
epidemic, and offering free biometric
health screenings. Other commenters
such as the Connecticut Business and
Industry Association and ValueCare
Alliance praised Aetna for providing
jobs and collaborating with providers on
74 TC-002.
75 TC-002,
TC-023, and TC-024.
TC-014, TC-015, TC-016, TC-017, TC020, TC-021, TC-023, TC-024, TC-025, TC-031, TC033, TC-044, TC-045, TC-047, TC-056, TC-059, TC060, TC-061, TC-062, TC-063, TC-064, TC-072, TC074, TC-078, TC-080, TC-081, TC-082, TC-085; see
also Amicus Brief from the AIDS Healthcare
Foundation, Dkt. # 50-1.
77 TC-007.
78 TC-065.
79 TC-005, TC-006, TC-008, TC-010, TC-018, TC019, TC-022, TC-028, TC-030, TC-036, TC-040, TC041, TC-042, TC-049, TC-051, TC-052, TC-053, TC055, TC-058, TC-069, TC-071, TC-073, TC-074, TC077, TC-079, TC-084.
76 TC-009,
E:\FR\FM\21FEN1.SGM
21FEN1
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Federal Register / Vol. 84, No. 35 / Thursday, February 21, 2019 / Notices
innovative healthcare products. These
comments are consistent with the
United States’ previous recognition that
this merger has the potential to generate
benefits by improving the quality and
lowering the costs of healthcare
services.80
VI. Conclusion
After careful consideration of the
public comments, the United States
continues to believe that the proposed
Final Judgment, as drafted, provides an
effective and appropriate remedy for the
antitrust violations alleged in the
Complaint, and is therefore in the
public interest. The United States will
move this Court to enter the proposed
Final Judgment after the comments and
this response are published as required
by 15 U.S.C. § 16(d).
amozie on DSK3GDR082PROD with NOTICES1
Dated: February 13, 2019
Respectfully submitted,
Jay D. Owen,
Shobitha Bhat,
Natalie R. Melada,
U.S. Department of Justice,
Antitrust Division,
450 Fifth Street NW, Suite 4100,
Washington, D.C. 20530,
Tel.: (202) 598-2987,
Fax: (202) 616-2441,
E-mail: Jay.Owen@usdoj.gov.
Registrants listed below has
applied for and been granted
registration by the Drug Enforcement
Administration (DEA) as importers of
schedule I or schedule II controlled
substances.
SUMMARY:
The
companies listed below applied to be
registered as importers of various basic
classes of controlled substances.
Information on the previously published
notices is listed in the table below. No
comments or objections were submitted
and no requests for hearing were
submitted for these notices.
SUPPLEMENTARY INFORMATION:
[FR Doc. 2019–02846 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–11–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Registration
ACTION:
Notice of registration.
Company
FR docket
Mylan Technologies, Inc. .............................................................................................................................
Noramco Inc. ................................................................................................................................................
Arizona Department of Corrections ..............................................................................................................
83 FR 64160
83 FR 64159
83 FR 64364
The DEA has considered the factors in
21 U.S.C. 823, 952(a) and 958(a) and
determined that the registration of the
listed registrants to import the
applicable basic classes of schedule I or
II controlled substances is consistent
with the public interest and with United
States obligations under international
treaties, conventions, or protocols in
effect on May 1, 1971. The DEA
investigated each company’s
maintenance of effective controls
against diversion by inspecting and
testing each company’s physical
security systems, verifying each
company’s compliance with state and
local laws, and reviewing each
company’s background and history.
Therefore, pursuant to 21 U.S.C.
952(a) and 958(a), and in accordance
with 21 CFR 1301.34, the DEA has
granted a registration as an importer for
schedule I or schedule II controlled
substances to the above listed
companies.
DEPARTMENT OF JUSTICE
Dated: January 29, 2019.
John J. Martin,
Assistant Administrator.
SUPPLEMENTARY INFORMATION:
[FR Doc. 2019–02871 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–09–P
80 See ‘‘Justice Department Requires CVS and
Aetna to Divest Aetna’s Medicare Individual Part D
VerDate Sep<11>2014
17:08 Feb 20, 2019
Jkt 247001
Drug Enforcement Administration
[Docket No. DEA–392]
Bulk Manufacturer of Controlled
Substances Application: Johnson
Matthey, Inc.
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic classes, and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before March 25, 2019. Such persons
may also file a written request for a
hearing on the application on or before
March 25, 2019.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
DATES:
Published
December 13, 2018.
December 13, 2018.
December 14, 2018.
implementation of 21 CFR part 1301,
incident to the registration of
manufacturers, distributors, dispensers,
importers, and exporters of controlled
substances (other than final orders in
connection with suspension, denial, or
revocation of registration) has been
redelegated to the Assistant
Administrator of the DEA Diversion
Control Division (‘‘Assistant
Administrator’’) pursuant to section 7 of
28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR
1301.33(a), this is notice that on October
12, 2018, Johnson Matthey Inc., 2003
Nolte Drive, West Deptford, New Jersey
08066, applied to be registered as a bulk
manufacturer of the following basic
classes of controlled substances listed in
schedule I & II.
Controlled substance
Drug
code
Schedule
The
Attorney General has delegated his
authority under the Controlled
Substances Act to the Administrator of
the Drug Enforcement Administration
(DEA), 28 CFR 0.100(b). Authority to
exercise all necessary functions with
respect to the promulgation and
Gamma Hydroxybutyric Acid.
Marihuana .................
Tetrahydrocannabinols.
Dihydromorphine ......
Difenoxin ...................
Amphetamine ...........
Methamphetamine ....
Lisdexamfetamine ....
Methylphenidate .......
Nabilone ...................
Prescription Drug Plan Business to Proceed with
Merger,’’ available at https://www.justice.gov/opa/
pr/justice-department-requires-cvs-and-aetnadivest-aetna-s-medicare-individual-part-d.
PO 00000
Frm 00074
Fmt 4703
Sfmt 4703
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I
7360
7370
I
I
9145
9168
1100
1105
1205
1724
7379
I
I
II
II
II
II
II
Agencies
[Federal Register Volume 84, Number 35 (Thursday, February 21, 2019)]
[Notices]
[Pages 5466-5477]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-02846]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Antitrust Division
United States, et al. v. CVS Health Corporation and Aetna Inc.;
Response to Public Comments
Pursuant to the Antitrust Procedures and Penalties Act, 15 U.S.C.
16(b)-(h), the United States hereby publishes below the Response to
Public Comments on the Proposed Final Judgment in United States, et al.
v. CVS Health Corporation and Aetna Inc., Civil Action No. 1:18-cv-
02340, which was filed in the United States District Court for the
District of Columbia on February 13, 2019, together with copies of the
173 comments received by the United States.
Pursuant to the Court's February 9, 2019 order, comments were
published electronically and are available to be viewed and downloaded
at the Antitrust Division's Web site, at: https://www.justice.gov/atr/us-v-cvs-health-corp-and-aetna-inc-index-comments. A copy of the United
States' response to the comments is also available at the same
location. Copies of the comments
[[Page 5467]]
and the United States' response are available for inspection at the
Office of the Clerk of the United States District Court for the
District of Columbia. Copies of these materials may also be obtained
from the Antitrust Division upon request and payment of the copying fee
set by Department of Justice regulations.
Patricia A. Brink,
Director of Civil Enforcement.
United States District Court for the District of Columbia
United States of America et al., Plaintiffs, v. CVS Health
Corporation and AETNA Inc., Defendants.
Case No. 1:18-cv-02340-RJL
RESPONSE OF PLAINTIFF UNITED STATES TO PUBLIC COMMENTS ON THE PROPOSED
FINAL JUDGMENT
Table of Contents
I. Introduction............................................ 1
II. Procedural History..................................... 2
III. Standard of Judicial Review........................... 2
IV. The Investigation, the Harm Alleged in the Complaint, 8
and the Proposed Final Judgment...........................
V. Summary of Public Comments and the United States' 12
Response..................................................
A. Comments Regarding WellCare's Suitability as a 13
Divestiture Buyer and Ability to Compete Effectively..
1. WellCare is an experienced and effective 13
competitor........................................
2. WellCare is an independent competitor to CVS.... 17
3. Prior health insurance merger remedies do not 19
cast doubt on the divestiture.....................
4. The remedy does not create new structural 21
concerns in the markets for individual PDPs.......
5. The licensing provisions related to the Aetna 23
brand protect WellCare's ability to compete using
the divested assets...............................
6. The sales price does not cast doubt on 23
WellCare's intention to compete...................
B. Comments Related to the Vertical Aspects of CVS's 24
Acquisition of Aetna..................................
1. Input foreclosure is unlikely to occur and is 26
beyond the scope of the Complaint.................
2. Customer foreclosure is unlikely to occur and is 27
beyond the scope of the Complaint.................
3. Vertical concerns are not addressable under the 29
Tunney Act's standard of review...................
C. Other Miscellaneous Comments........................ 30
D. Comments in Support of the Merger................... 34
VI. Conclusion............................................. 35
I. Introduction
As required by the Antitrust Procedures and Penalties Act (the
``APPA'' or ``Tunney Act''), 15 U.S.C. Sec. Sec. 16(b)-(h), the United
States hereby responds to the public comments received about the
proposed Final Judgment in this case. After careful consideration of
the comments, the United States continues to believe that the proposed
remedy will address the harm alleged in the Complaint and is therefore
in the public interest.
The remedy preserves competition for the approximately 21 million
beneficiaries who purchase individual prescription drug plans
(``individual PDPs'') in the United States. The remedy fully addresses
the competitive threat posed by the merger by requiring CVS to divest
Aetna's nationwide individual PDP business to WellCare Health Plans,
Inc., an experienced health insurer focused on government-sponsored
health plans, including individual PDPs. By requiring a nationwide
divestiture, the remedy provides WellCare with the assets and scale
necessary to maintain competition in the 16 regions identified in the
Complaint. The remedy also provides WellCare with access to all of the
records, employees, and other rights necessary to ensure that WellCare
can step into Aetna's shoes. The remedy thus preserves the competition
that otherwise would be lost through the merger and ensures that
WellCare will effectively replace Aetna as an independent and vigorous
competitor.
The United States received 173 comments about the proposed remedy
reflecting a wide range of views. Some comments supported the merger.
Other comments acknowledged the significant scope of the divestiture,
but expressed concerns about the divestiture buyer. Many comments
raised issues that are outside the scope of the Tunney Act review.
After careful consideration of these comments, the United States
maintains that the remedy in the proposed Final Judgment provides
comprehensive relief that satisfies the Tunney Act's public-interest
standard.
The United States will publish the comments and this response on
the Antitrust Division's website and is submitting to the Federal
Register this response and the website address at which the comments
may be viewed and downloaded, as authorized by the Court's order dated
February 9, 2019. Following Federal Register publication, the United
States will move the Court to enter the proposed Final Judgment.
II. Procedural History
On December 3, 2017, CVS entered into an agreement to acquire Aetna
in a merger valued at approximately $69 billion. On October 10, 2018,
the United States filed a civil antitrust Complaint seeking to enjoin
CVS from acquiring Aetna because the proposed acquisition would
substantially lessen competition for the sale of individual PDPs in 16
regions in the United States in violation of Section 7 of the Clayton
Act, 15 U.S.C. Sec. 18.
Simultaneously with the filing of the Complaint, the United States
filed a proposed Final Judgment, a Stipulation signed by the parties
that consents to entry of the proposed Final Judgment after compliance
with the requirements of the Tunney Act, and a Competitive Impact
Statement describing the transaction and the proposed Final Judgment.
The United States caused the Complaint, the proposed Final Judgment,
and Competitive Impact Statement to be published in the Federal
Register on October 17, 2018, see 83 Fed. Reg. 52558 (October 17,
2018), and caused notice regarding the same, together with directions
for the submission of written comments relating to the proposed Final
Judgment, to be published in The Washington Post on October 12-18,
2018. The 60-day period for public comment ended on December 17, 2018.
III. Standard of Judicial Review
The Clayton Act, as amended by the APPA, requires that proposed
consent judgments in antitrust cases brought by
[[Page 5468]]
the United States be subject to a 60-day comment period, after which
the court shall determine whether entry of the proposed Final Judgment
``is in the public interest.'' 15 U.S.C. Sec. 16(e)(1). In making that
determination, the court, in accordance with the statute as amended in
2004, is required to consider:
(A) the competitive impact of such judgment, including
termination of alleged violations, provisions for enforcement and
modification, duration of relief sought, anticipated effects of
alternative remedies actually considered, whether its terms are
ambiguous, and any other competitive considerations bearing upon the
adequacy of such judgment that the court deems necessary to a
determination of whether the consent judgment is in the public
interest; and
(B) the impact of entry of such judgment upon competition in the
relevant market or markets, upon the public generally and
individuals alleging specific injury from the violations set forth
in the complaint including consideration of the public benefit, if
any, to be derived from a determination of the issues at trial.
15 U.S.C. Sec. 16(e)(1)(A) & (B). In considering these statutory
factors, the court's inquiry is necessarily a limited one as the
government is entitled to ``broad discretion to settle with the
defendant within the reaches of the public interest.'' United States v.
Microsoft Corp., 56 F.3d 1448, 1461 (D.C. Cir. 1995); see generally
United States v. SBC Commc'ns, Inc., 489 F. Supp. 2d 1 (D.D.C. 2007)
(assessing public-interest standard under the Tunney Act); United
States v. U.S. Airways Group, Inc., 38 F. Supp. 3d 69, 75 (D.D.C. 2014)
(explaining that the ``court's inquiry is limited'' in Tunney Act
settlements); United States v. InBev N.V./S.A., No. 08-1965 (JR), 2009
U.S. Dist. LEXIS 84787, at *3 (D.D.C. Aug. 11, 2009) (noting that the
court's review of a consent judgment is limited and only inquires
``into whether the government's determination that the proposed
remedies will cure the antitrust violations alleged in the complaint
was reasonable, and whether the mechanism to enforce the final judgment
are clear and manageable'').
As the U.S. Court of Appeals for the District of Columbia Circuit
has held, under the APPA a court considers, among other things, the
relationship between the remedy secured and the specific allegations in
the government's complaint, whether the decree is sufficiently clear,
whether its enforcement mechanisms are sufficient, and whether the
decree may positively harm third parties. See Microsoft, 56 F.3d at
1458-62. With respect to the adequacy of the relief secured by the
decree, a court may not ``engage in an unrestricted evaluation of what
relief would best serve the public.'' United States v. BNS, Inc., 858
F.2d 456, 462 (9th Cir. 1988) (quoting United States v. Bechtel Corp.,
648 F.2d 660, 666 (9th Cir. 1981)); see also Microsoft, 56 F.3d at
1460-62; United States v. Alcoa, Inc., 152 F. Supp. 2d 37, 40 (D.D.C.
2001); InBev, 2009 U.S. Dist. LEXIS 84787, at *3. Instead:
[t]he balancing of competing social and political interests affected
by a proposed antitrust consent decree must be left, in the first
instance, to the discretion of the Attorney General. The court's
role in protecting the public interest is one of insuring that the
government has not breached its duty to the public in consenting to
the decree. The court is required to determine not whether a
particular decree is the one that will best serve society, but
whether the settlement is ``within the reaches of the public
interest.'' More elaborate requirements might undermine the
effectiveness of antitrust enforcement by consent decree.
Bechtel, 648 F.2d at 666 (emphasis added) (citations omitted).\1\
---------------------------------------------------------------------------
\1\ See also BNS, 858 F.2d at 464 (holding that the court's
``ultimate authority under the [APPA] is limited to approving or
disapproving the consent decree''); United States v. Gillette Co.,
406 F. Supp. 713, 716 (D. Mass. 1975) (noting that, in this way, the
court is constrained to ``look at the overall picture not
hypercritically, nor with a microscope, but with an artist's
reducing glass'').
---------------------------------------------------------------------------
In determining whether a proposed settlement is in the public
interest, a district court ``must accord deference to the government's
predictions about the efficacy of its remedies, and may not require
that the remedies perfectly match the alleged violations.'' SBC
Commc'ns, 489 F. Supp. 2d at 17; see also U.S. Airways, 38 F. Supp. 3d
at 74-75 (noting that a court should not reject the proposed remedies
because it believes others are preferable and that room must be made
for the government to grant concessions in the negotiation process for
settlements); Microsoft, 56 F.3d at 1461 (noting the need for courts to
be ``deferential to the government's predictions as to the effect of
the proposed remedies''); United States v. Archer-Daniels-Midland Co.,
272 F. Supp. 2d 1, 6 (D.D.C. 2003) (noting that the court should grant
``due respect to the government's prediction as to the effect of
proposed remedies, its perception of the market structure, and its
views of the nature of the case''). The ultimate question is whether
``the remedies [obtained in the decree are] so inconsonant with the
allegations charged as to fall outside of the `reaches of the public
interest.' '' Microsoft, 56 F.3d at 1461 (quoting United States v.
Western Elec. Co., 900 F.2d 283, 309 (D.C. Cir. 1990)). To meet this
standard, the United States ``need only provide a factual basis for
concluding that the settlements are reasonably adequate remedies for
the alleged harms.'' SBC Commc'ns, 489 F. Supp. 2d at 17.
Moreover, under Microsoft, the court's role under the APPA is
limited to reviewing the remedy in relationship to the violations that
the United States has alleged in its complaint, and does not authorize
the court to ``construct [its] own hypothetical case and then evaluate
the decree against that case.'' Microsoft, 56 F.3d at 1459; see also
U.S. Airways, 38 F. Supp. 3d at 75 (noting that the court must simply
determine whether there is a factual foundation for the government's
decisions such that its conclusions regarding the proposed settlements
are reasonable); InBev, 2009 U.S. Dist. LEXIS 84787, at *20 (``the
`public interest' is not to be measured by comparing the violations
alleged in the complaint against those the court believes could have,
or even should have, been alleged''). Because the ``court's authority
to review the decree depends entirely on the government's exercising
its prosecutorial discretion by bringing a case in the first place,''
it follows that ``the court is only authorized to review the decree
itself,'' and not to ``effectively redraft the complaint'' to inquire
into other matters that the United States did not pursue. Microsoft, 56
F.3d at 1459-60. To inquire about claims that are not in a complaint
would violate the separation of powers and aggravate the
``constitutional difficulties that inhere in this statute.'' See United
States' December 14, 2018 Response to Order to Show Cause, Dkt. #32 at
3-7 (discussing the constitutional difficulties with the Tunney Act);
see also Microsoft 56 F.3d at 1459; United States v. Fokker Servs., 818
F.3d 733, 738 (D.C. Cir. 2016) (recognizing the ``long-settled
understandings about the independence of the Executive with regard to
charging decisions''); Heckler v. Chaney, 470 U.S. 821, 832 (1985)
(quoting U.S. Const. art. II, Sec. 3) (recognizing that the decision
about which claims to bring ``has long been regarded as the special
province of the Executive Branch.'').
An amicus brief filed by the AIDS Healthcare Foundation erroneously
argues that the 2004 amendments to the Tunney Act overrule Microsoft,
allowing courts to consider allegations that are not in the
complaint.\2\ In fact, however, the amendments addressed a separate
issue. In the Microsoft opinion, after the court held that the Tunney
Act does not allow courts to look beyond the
[[Page 5469]]
scope of the complaint, the opinion says that a district judge is not
obliged to accept a consent decree that ``appears to make a mockery of
judicial power.'' 56 F.3d at 1462. According to legislative history of
the 2004 amendments, Congress was concerned that subsequent courts had
taken this latter language too far, limiting their review solely to the
question of whether ``antitrust consent judgments'' would make ``a
mockery of the judicial function.'' \3\ As a result, Congress changed
the language of Sec. 16(e) from saying that the court ``may'' consider
the public-interest factors to the court ``shall'' consider those
factors, making them mandatory.\4\ Congress also modified the list of
factors, for example, adding a new factor (whether the terms of the
judgment are ambiguous \5\), which the Microsoft court had already made
clear was appropriate to consider, 56 F.3d at 1461-62. Thus, as Senator
Hatch observed, ``this amendment essentially codifies existing case
law.'' \6\ See also SBC Commc'ns, 489 F. Supp. 2d at 11 (concluding
that the 2004 amendments ``effected minimal changes'' to the Tunney Act
review).
---------------------------------------------------------------------------
\2\ Amicus Brief from the AIDS Healthcare Foundation, Dkt. #50-
1.
\3\ Antitrust Criminal Penalty Enhancement and Reform Act of
2004, Pub. L. No. 108-237, tit. II, Sec. 221(a), 118 Stat. 661, 668
(2004) (finding that ``it would misconstrue the meaning and
Congressional intent in enacting the Tunney Act to limit the
discretion of district courts to review antitrust consent judgments
solely to determining whether entry of those consent judgments would
make a `mockery of the judicial function.' '').
\4\ Compare 15 U.S.C. Sec. 16(e) (2004), with 15 U.S.C. Sec.
16(e)(1) (2006).
\5\ 15 U.S.C. Sec. 16 (e)(1)(A).
\6\ 150 Cong. Rec. S3610, at S3613 (daily ed. Apr. 2, 2004).
---------------------------------------------------------------------------
Indeed, rather than overruling Microsoft, the 2004 amendments
reaffirm that courts should focus solely on how the judgment impacts
the harms alleged in the complaint by (1) keeping the language in Sec.
16(e) that directs courts to limit their analysis to the competitive
impact of the ``consent judgment,'' \7\ (2) adding language that
directs courts to consider competition ``in the relevant market or
markets,'' \8\ and (3) making those considerations mandatory rather
than permissive. As Senator Kohl's floor statement explained, ``A
mandate to review the impact of entry of the consent judgment upon
`competition in the relevant market or markets' . . . will ensure that
the Tunney Act review is properly focused on the likely competitive
impact of the judgment, rather than extraneous factors irrelevant to
the purposes of antitrust enforcement.'' \9\
---------------------------------------------------------------------------
\7\ 15 U.S.C. Sec. 16(e)(1).
\8\ Compare 15 U.S.C. Sec. 16(e) (2004), with 15 U.S.C. Sec.
16(e)(1)(B) (2006).
\9\ 150 Cong. Rec. S3618 (statement of Sen. Kohl).
---------------------------------------------------------------------------
Finally, in the 2004 amendments, Congress addressed the Tunney Act
review process, adding the unambiguous instruction that ``[n]othing in
this section shall be construed to require the court to conduct an
evidentiary hearing or to require the court to permit anyone to
intervene.'' 15 U.S.C. Sec. 16(e)(2); see also U.S. Airways, 38 F.
Supp. 3d at 76 (indicating that a court is not required to hold an
evidentiary hearing or to permit intervenors as part of its review
under the Tunney Act). This language explicitly wrote into the statute
what Congress intended when it first enacted the Tunney Act in 1974. As
Senator Tunney explained: ``[t]he court is nowhere compelled to go to
trial or to engage in extended proceedings which might have the effect
of vitiating the benefits of prompt and less costly settlement through
the consent decree process.'' 119 Cong. Rec. 24,598 (1973) (statement
of Sen. Tunney). Rather, the procedure for the public-interest
determination is left to the discretion of the court, with the
recognition that the court's ``scope of review remains sharply
proscribed by precedent and the nature of Tunney Act proceedings.'' SBC
Commc'ns, 489 F. Supp. 2d at 11. A court can make its public-interest
determination based on the competitive impact statement and response to
public comments alone. U.S. Airways, 38 F. Supp. 3d at 76; see also
United States v. Enova Corp., 107 F. Supp. 2d 10, 17 (D.D.C. 2000)
(noting that the ``Tunney Act expressly allows the court to make its
public interest determination on the basis of the competitive impact
statement and response to comments alone''); S. Rep. No. 93-298 93d
Cong., 1st Sess., at 6 (1973) (``Where the public interest can be
meaningfully evaluated simply on the basis of briefs and oral
arguments, that is the approach that should be utilized.'').
IV. The Investigation, the Harm Alleged in the Complaint, and the
Proposed Final Judgment
The proposed Final Judgment is the culmination of a thorough,
comprehensive investigation conducted by the Antitrust Division of the
U.S. Department of Justice into CVS's proposed acquisition of Aetna. As
noted in the Complaint, CVS is one of the largest companies in the
United States. It operates the nation's largest retail pharmacy chain.
It owns a large pharmacy benefit manager (``PBM'') called Caremark,
which manages the pharmacy benefits for various health plans and
negotiates their drug pricing with pharmaceutical companies and retail
pharmacies. Through its subsidiary called SilverScript, CVS is also the
nation's largest provider of individual PDPs, which provide Medicare
beneficiaries with insurance coverage for their prescription drugs.
Aetna is the nation's third largest health insurer and, before the
divestiture, offered individual PDPs throughout the United States.
Based on the evidence gathered during its investigation, the United
States concluded that CVS's proposed acquisition of Aetna would likely
substantially lessen competition for the sale of individual PDPs in the
16 geographic regions where CVS and Aetna are particularly strong,
resulting in higher prices, less innovation, fewer choices, and lower-
quality individual PDPs for Medicare beneficiaries in these regions.
Accordingly, the United States filed a civil antitrust lawsuit to block
the acquisition as a violation of Section 7 of the Clayton Act, 15
U.S.C. Sec. 18.
The proposed Final Judgment provides an effective and appropriate
remedy for the transaction's likely competitive harm by requiring CVS
to divest Aetna's individual PDP business nationwide. The proposed
Final Judgment has several components, which the parties agreed to
abide by during the pendency of the Tunney Act proceeding, and which
the Court ordered in the Asset Preservation Stipulation and Order of
October 25, 2018, Dkt. 15.
First, CVS must divest both of Aetna's individual PDP contracts
with the Centers for Medicare and Medicaid Services (``CMS''), which is
the federal agency that administers the PDP program. Aetna's individual
PDP business was the only portion of Aetna's business where the merger
with CVS would have caused a substantial lessening of competition.
Divesting Aetna's nationwide individual PDP business--and not just
Aetna's business in the regions identified in the Complaint--provides
WellCare with the same scale and capabilities to implement a national
PDP strategy as Aetna had before the merger. Aetna's individual PDP
contracts were transferred to WellCare on November 29, 2018. From
December 2018 to January 2019, WellCare's enrollment in its legacy PDP
plans increased by over 400,000 members nationwide, and its market
share grew in all 34 PDP regions. The enrollment in the divested Aetna
plans also grew, adding over 140,000 members.\10\
---------------------------------------------------------------------------
\10\ See CMS Monthly Enrollment by CPSC for January 2019,
available at https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports/MCRAdvPartDEnrolData/Monthly-Enrollment-by-Contract-Plan-State-County-Items/Monthly-Enrollment-by-CPSC-2019-01.html?DLPage=1&DLEntries=10&DLSort=1&DLSortDir=descending.
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[[Page 5470]]
Second, the proposed Final Judgment requires CVS and Aetna to
transfer to WellCare (1) data relating to Aetna's individual PDP
business, (2) information regarding the amount that Aetna pays to
retail pharmacies in exchange for filling prescriptions for Aetna
members, and (3) any contracts with brokers that currently sell Aetna's
individual PDPs. The transfer of this data, information, and contracts
helps ensure that WellCare has sufficient information to negotiate with
retail pharmacies and brokers on the same footing as Aetna did before
the merger.
Third, during the 60-day period following the sale to WellCare, the
proposed Final Judgment has provided WellCare the opportunity to
interview and hire Aetna's current employees with expertise related to
the individual PDP business. The transfer of data and recruiting of
Aetna employees are moving forward according to the terms of the
proposed Final Judgment.
The proposed Final Judgment also includes provisions aimed at
ensuring that the divested assets are handed off in a seamless and
efficient manner, particularly for the two key competitive events for
individual PDPs: the submission of bids to CMS each June (for the
following year) and open-enrollment season for members, which occurs
from October through December. In this case, before the contracts were
transferred to WellCare on November 29, 2018, Aetna had already
submitted its bids for the divestiture assets and open-enrollment was
well under way. Thus, to assist WellCare during the 2019 plan year, CVS
must, at WellCare's option, enter into an administrative services
agreement to provide WellCare with all of the services required to
manage the divestiture assets through the plan year, which ends on
December 31, 2019. These services include contracting with pharmacy
networks, administering the plans' formularies, and providing back-
office support and claims administration functions. Requiring CVS to
support and service these plans provides continuity to members who
purchased an Aetna individual PDP during the open-enrollment period
that ran from October through December 2018 and will ensure that
members receive the plans that they have chosen. CVS and WellCare have
entered into an administrative services agreement and, since the
divestiture, CVS has been providing WellCare with the necessary
services to manage the divestiture assets in 2019 while WellCare has
begun preparing for the June 2019 submission of its bid for 2020.
Additionally, CVS and Aetna must allow WellCare to use the Aetna
brand for the divestiture assets through December 31, 2019, and CVS and
Aetna are prohibited, through 2020, from using the Aetna brand for the
CVS individual PDP business that they are retaining. This will provide
WellCare with a window to establish a relationship with current Aetna
individual PDP beneficiaries and avoid customer confusion.
The proposed Final Judgment also includes robust mechanisms that
will allow the United States and the Court to monitor the effectiveness
of the relief and to enforce compliance. For example, the proposed
Final Judgment provides for the appointment of a monitoring trustee,
which the Court appointed on December 3, 2018. As a result, the
monitoring trustee, Ms. Julie Myers Wood, is actively working to ensure
that the divestiture proceeds appropriately. She has the power and
authority to investigate and report on Defendants' compliance with the
terms of the Final Judgment and the Asset Preservation Stipulation and
Order during the pendency of the divestiture and is required to file
reports with the United States every 90 days. In addition, the proposed
Final Judgment provides the United States with the ability to
investigate Defendants' compliance with the Final Judgment and
expressly retains and reserves all rights for the United States to
enforce the provisions of the proposed Final Judgment, including its
rights to seek an order of contempt from the Court.
Together, the requirements in the proposed Final Judgment ensure
that WellCare can step into Aetna's shoes, thereby preserving the
competition that the merger would otherwise destroy.
V. Summary of Public Comments and the United States' Response
The United States received 173 comments \11\ from different
categories of commenters. These commenters included advocacy groups,
such as the American Medical Association (``AMA''), the American
Antitrust Institute (``AAI''), Consumer Action and U.S. PIRG, and the
Medical Society of the State of New York (``MSSNY''). In addition, the
United States received comments from several groups representing
pharmacists that compete with CVS, including the National Community
Pharmacists Association (``NCPA''), the Pharmacists Society of the
State of New York (``PSSNY''), and Pharmacists United for Truth and
Transparency (``PUTT''), as well as approximately 120 individual
pharmacies. The United States also received a handful of comments from
business associations and healthcare industry associations.
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\11\ These comments are provided as attachments TC-001 through
TC-085. Aside from redactions of personally identifiable information
such as personal email addresses, phone numbers, and patient
information, the comments are provided in their entirety. Four
groups of substantially similar comments are included together as
attachments TC-007, TC-020, TC-057 and TC-061. Amicus filings made
before the end of the comment period by (1) Consumer Action and U.S.
PIRG and (2) PUTT and PSSNY are included as attachments TC-023 and
TC-060, respectively.
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The comments can be grouped into four categories: (1) comments
about WellCare's suitability as a divestiture buyer, including whether
it will have sufficient assets, expertise, and incentives to preserve
competition; (2) comments related to the vertical combination of CVS's
pharmacy and PBM businesses with Aetna's health insurance businesses;
(3) other miscellaneous comments, including questions about whether the
merger will facilitate coordination, have anticompetitive effects in
various healthcare markets, increase entry barriers in the PBM or
health insurance markets, or reduce PBM competition by eliminating
Aetna as a PBM competitor; and (4) comments in support of the merger.
The Court's analysis under the Tunney Act should focus on the first
category of comments, as they are the only comments that relate to
whether the proposed remedy addresses the harms alleged in the
Complaint. See Microsoft, 56 F.3d at 1459.
A. Comments Regarding WellCare's Suitability as a Divestiture Buyer and
Ability to Compete Effectively
WellCare has extensive experience and qualifications in the
individual PDP market and, with the assets provided by the proposed
Final Judgment, is a suitable divestiture buyer. Although the AMA,
Consumer Action and U.S. PIRG, NCPA, PUTT and PSSNY, and numerous
independent pharmacies, raised concerns regarding WellCare as the buyer
of the divested assets, none of those concerns is valid for the reasons
explained below.\12\ These commenters raised six primary objections:
(1) WellCare will not compete as effectively as Aetna; (2) WellCare
will not operate independently of CVS because WellCare uses CVS's PBM,
Caremark; (3) some
[[Page 5471]]
health insurance divestitures have not been successful, indicating that
the divestiture to WellCare may not be successful; (4) the divestiture
creates new structural concerns in the markets for the sale of
individual PDPs; (5) the divestiture raises concerns related to
WellCare's license of the Aetna brand; and (6) the divestiture sales
price is too low.
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\12\ TC-003, TC-015, TC-023, TC-024, TC-047, TC-054, TC-059, TC-
060, TC-061, TC-063, TC-064, TC-072, TC-080, TC-081, and TC-085.
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1. WellCare is an experienced and effective competitor.
WellCare has experience and qualifications in government-funded
insurance programs. Despite this, commenters said that WellCare may not
compete as effectively as Aetna in individual PDP markets because
WellCare is smaller and less capable than Aetna and because WellCare is
not purchasing a stand-alone business unit; these concerns are
misplaced.\13\ Although Aetna's overall membership is larger when
taking into account its commercial business, WellCare is already a
large and established insurer that has competed in the markets for
individual PDPs for over a decade. WellCare is a Fortune 200 company
with over 12,000 employees, 5.5 million members, and a market
capitalization of approximately $15 billion. Even before acquiring over
2.1 million members from Aetna as part of the divested business,
WellCare had attracted nearly 1.1 million individuals in its PDPs
throughout the United States. WellCare is thus starting from a strong
base and its acquisition of all of Aetna's individual PDP business will
enable WellCare to improve its PDP business and become a more
significant competitor.
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\13\ See, e.g., TC-003, TC-024, and TC-060.
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Some commenters expressed a concern that, despite its size,
WellCare will not be as competitive as Aetna because Aetna's overall
health insurance business was larger than that of WellCare.\14\ Before
the divestiture, however, WellCare already competed successfully as a
smaller competitor than Aetna. From 2018 to 2019, WellCare organically
grew its business by over 40 percent, from approximately 1 million
members to over 1.4 million members.\15\ More importantly, with the
acquisition of Aetna's individual PDP business, WellCare's total
individual PDP membership is well over three million members,
approximately 50 percent more than Aetna's pre-divestiture individual
PDP membership. Following the divestiture, WellCare will be well-
positioned to achieve any benefits of scale that Aetna had enjoyed in
its individual PDP business, enabling it to be an even more formidable
competitor than it previously was and ensuring that the remedy is well
within the ``reaches of the public interest,'' as required under the
Tunney Act. See Microsoft, 56 F.3d at 1461.
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\14\ See, e.g., TC-003, TC-024.
\15\ See CMS Monthly Enrollment by CPSC for January 2019,
available at https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports/MCRAdvPartDEnrolData/Monthly-Enrollment-by-Contract-Plan-State-County-Items/Monthly-Enrollment-by-CPSC-2019-01.html?DLPage=1&DLEntries=10&DLSort=1&DLSortDir=descending.
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Concerns that WellCare is not getting enough assets or a stand-
alone business unit from Aetna misunderstand the context of the remedy
here.\16\ The Antitrust Division's experience, as reflected in the 2004
Policy Guide to Merger Remedies,\17\ is that in some instances, an in-
market buyer does not need a stand-alone business unit to be
successful: ``The Division will approve the divestiture of less than an
existing business entity if the evidence clearly demonstrates that
certain of the entity's assets already are in the possession of, or
readily obtainable in a competitive market by, the potential
purchaser.''\18\
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\16\ See, e.g., TC-024, TC-060.
\17\ This is the operative guide on remedies following the
September 25, 2018 withdrawal of the 2011 Policy Guide to Merger
Remedies. See Makan Delrahim, It Takes Two: Modernizing the Merger
Review Process, Remarks at the 2018 Global Antitrust Enforcement
Symposium (September 25, 2018), available at https://www.justice.gov/opa/speech/assistant-attorney-general-makan-delrahim-delivers-remarks-2018-global-antitrust.
\18\ Antitrust Division Policy Guide to Merger Remedies, October
2004, at 14, available at https://www.justice.gov/sites/default/files/atr/legacy/2011/06/16/205108.pdf.
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Consistent with this principle, the proposed Final Judgment ensures
that WellCare will have all that it needs to preserve competition in
the sale of individual PDPs. WellCare has purchased Aetna's entire
individual PDP business throughout the United States, including the
relevant contracts, the right to hire employees, and access to all
relevant data. Focusing on a stand-alone ``business unit'' in this case
ignores the critical fact that WellCare already offers individual PDPs
throughout the United States, is licensed in all 50 states, and has
scalable in-house capabilities that it does not need to duplicate.
These capabilities include experience competing in individual PDP
markets throughout the country, actuarial expertise, as well as
clinical and administrative resources. Because of these existing
capabilities, WellCare does not need to acquire a stand-alone business
unit to compete for the sale of individual PDPs. Instead, WellCare is
acquiring key competitive assets that complement its existing
capabilities and allow WellCare to step quickly and effectively into
Aetna's shoes as a significant competitor for the sale of individual
PDPs.
Despite WellCare's in-market expertise, the joint comments by
Consumer Action and U.S. PIRG \19\ and PUTT and PSSNY \20\ erroneously
argue that WellCare is similarly situated to Molina, the proposed
divestiture buyer of Aetna's Medicare Advantage business that Judge
Bates rejected in an opinion enjoining Aetna's proposed acquisition of
Humana.\21\ This concern fails to appreciate that WellCare is
differently situated than Molina in several ways. Unlike Molina, which
had ``made forays into the individual Medicare Advantage market'' but
never succeeded,\22\ WellCare has consistently maintained a presence in
the individual PDP business since the program's inception in 2006.
Also, Aetna proposed to divest only small portions of each of the
merging parties' Medicare Advantage business to Molina. In contrast,
while WellCare has not purchased a stand-alone business unit, it has
purchased Aetna's entire individual PDP business, including Aetna's
business outside the affected geographic markets. Medicare Advantage
products also differ significantly from individual PDP products. In
addition to the pharmacy networks used by PDPs, Medicare Advantage
products require a comprehensive network of hospitals, doctors, and
other healthcare providers at competitive rates. In Aetna/Humana,
Molina had no presence at all in 89 percent of the counties referenced
in the United States' complaint and no Medicare presence in 95 percent
of the counties, so the company would have needed to build its own
provider network to compete in the market.\23\ By contrast, WellCare
already has an extensive pharmacy network that it uses to sell
individual PDPs throughout the United States and will not have to
assemble any new networks in any region to offer individual PDPs. Thus,
unlike Molina in Aetna/Humana, WellCare is both purchasing an entire
business and is a qualified buyer with the assets and capabilities to
continue competing successfully.
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\19\ TC-023 at 3-4, TC-024 at 5-6.
\20\ TC-060 at 21.
\21\ United States v. Aetna, Inc., 240 F. Supp. 3d 1, 73 (D.D.C.
2017).
\22\ Id. at 62.
\23\ Id. at 65.
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[[Page 5472]]
2. WellCare is an independent competitor to CVS.
Although some commenters raised concerns that WellCare will not
operate independently of CVS because WellCare uses Caremark (which CVS
owns) as its PBM,\24\ the United States carefully considered this
relationship in evaluating WellCare's suitability as the divestiture
buyer and ultimately concluded that WellCare will continue to be an
independent competitor to CVS for several reasons.
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\24\ See, e.g., TC-003, TC-015, TC-060, TC-061, and TC-080.
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First, CVS has no governance control over WellCare. Rather,
WellCare is a separate corporate entity with an independent board of
directors. Second, CVS and WellCare do not have common financial
incentives. As a separate company, WellCare is driven to focus on its
own business and compete vigorously against CVS. Third, while WellCare
may make the independent business decision to use Caremark rather than
its other PBM options, nothing in the proposed Final Judgment requires
WellCare to do so. In fact, WellCare recently announced that it is
putting its PBM services contract out to bid in the summer of 2019.\25\
Fourth, WellCare recently acquired a small PBM called Meridian, which
improves WellCare's ability to provide its own PBM services. Finally,
Caremark's business has internal firewalls designed to prevent
insurance customers' information from being shared with SilverScript
and other insurance customers. This means that WellCare, like all of
Caremark's health plan customers, can make its own independent business
decisions with the protections these firewalls provide against the risk
that SilverScript, or any other Caremark customer, will have access to
competitively sensitive information or advance knowledge of its
business plans and other competitive decisions.
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\25\ See ``WellCare Fourth Quarter 2018 Earnings Conference Call
Transcript'' (February 5, 2019) available at https://www.fool.com/earnings/call-transcripts/2019/02/05/wellcare-health-plans-inc-wcg-q4-2018-earnings-con.aspx (last visited February 13, 2019).
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Because WellCare retains control of the divestiture assets and has
the financial incentive to use them in its best interests, rather than
CVS's, WellCare's relationship with Caremark does not change the
conclusion that the proposed remedy is in the public interest. This
conclusion is bolstered by the success of Aetna's individual PDP plans,
which used Caremark for PBM services before the merger, showing that a
relationship with Caremark does not impede an individual PDP's
competitiveness. Similarly, WellCare has also competed against CVS's
SilverScript business for many years despite using Caremark for PBM
services.
Other comments incorrectly suggest that, because the proposed Final
Judgment includes transition services agreements for 2019, WellCare
will not operate the divestiture assets independently of CVS.\26\ As
described above, the proposed Final Judgment requires that, at
WellCare's option, CVS must enter into an administrative services
agreement to provide WellCare with all of the services required to
manage the divestiture assets through the 2019 plan year. CVS must
offer these services at the direction of WellCare and subject to the
review of both the monitoring trustee and the United States, whose
oversight will likely deter any attempts to undermine WellCare's
competitiveness.
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\26\ TC-003, TC-023, and TC-024.
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The transition services agreements are also only in place through
2019. This temporary arrangement provides continuity to members who
purchased an Aetna individual PDP during the open-enrollment period
that ran from October through December 2018, but ends when plans for
2020 will become effective. These transition services are necessary for
the seamless and efficient transition of Aetna's individual PDP
business to WellCare. Importantly, the agreements do not affect the
prices, design, coverage amounts, and other terms of the plans WellCare
is now offering to seniors. Rather, these terms have been fixed for all
of 2019.
Further, the monitoring trustee is closely tracking CVS's
compliance with the terms of the transition services agreements. CVS's
obligations are clearly stated in the proposed Final Judgment, and the
monitoring trustee is already ensuring that CVS is fulfilling its
responsibilities. Because Aetna's contracts with CMS, as well as the
related data, have been transferred in accordance with the terms of the
proposed Final Judgment, WellCare has all the assets it needs to
independently prepare for the next competitive event--the June 2019
submission of the bid for 2020--which is not impacted by the transition
services agreements.
3. Prior health insurance merger remedies do not cast doubt on the
divestiture.
In 2012, the United States required Humana Inc. and Arcadian
Management Services Inc. to divest assets relating to Arcadian's
Medicare Advantage business in 51 counties in five states in order for
Humana to proceed with an acquisition of Arcadian.\27\ Several
commenters looked at this and other divestitures in hindsight and
conclude that they failed or that divestitures in general are not
successful remedies.\28\ As a general matter, however, the factual
circumstances in every divestiture are different. Furthermore, the
concerns that the experience of prior divestitures indicates that the
divestiture to WellCare will fail in this instance are wrong because
the circumstances here are different.
---------------------------------------------------------------------------
\27\ See ``Justice Department Requires Divestitures in Humana
Inc.'s Acquisition of Arcadian Management Services Inc.,'' available
at https://www.justice.gov/opa/pr/justice-department-requires-divestitures-humana-incs-acquisition-arcadian-management-services.
\28\ TC-003, TC-023, TC-024, and TC-060.
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Indeed, there are several key differences between this divestiture
and the ones in Humana/Arcadian, the most important of which is the
scope of the divestiture. In Humana/Arcadian the divestiture did not
constitute an entire business, as it included only 12,700 covered lives
in 51 rural counties and was split between three different acquirers.
In contrast, CVS has divested Aetna's entire individual PDP business,
consisting of over two million members and including assets outside the
markets described in the Complaint. Additionally, similar to Molina in
Aetna/Humana, the Humana/Arcadian divestitures concerned Medicare
Advantage products and some of those divestitures went to buyers that
did not have Medicare Advantage provider networks in the divested
markets. In contrast, WellCare already has pharmacy networks in every
region of the United States. Divesting the entire line of business to
WellCare, a well-positioned buyer, will help ensure that WellCare
continues to compete effectively and capture additional economies of
scale across its entire business.
Despite these factual differences, commenters also note that
WellCare was the buyer of one set of divested assets in Humana/Arcadian
and wrongly suggest that, because that divestiture failed, this one
likely will too.\29\ As described above, the two divestitures are
substantially different. In Humana/Arcadian, WellCare acquired fewer
than 5,000 lives in two counties in Arizona. In contrast, WellCare is
acquiring over 2.1 million individual PDP lives across the United
States from Aetna. Additionally, as described above,
[[Page 5473]]
WellCare did not have a Medicare Advantage provider network in Arizona
before the divestiture in Humana/Arcadian while WellCare already has an
established pharmacy network in place that it can use for the PDP
business it is acquiring from Aetna. Further, WellCare has grown
significantly as a company since 2012--more than doubling from 2.7
million \30\ members to 5.5 million \31\--and overhauled its leadership
team, including the CEO, CFO, CIO, CMO, and the EVP for Clinical
Operations.\32\ Because of the larger scale of the current divestiture,
WellCare's growth as a health insurance company, and its experience and
existing capabilities with individual PDPs, WellCare's performance with
the Humana/Arcadian assets does not indicate how successful it will be
with Aetna's PDP business. Because a district court ``must accord
deference to the government's predictions about the efficacy of its
remedies,'' SBC Commc'ns, 489 F. Supp. 2d at 17, and because the
divestiture to WellCare is readily distinguishable from the ones that
commenters allege failed in Humana/Arcadian, the Court should afford
deference to the government's prediction of a successful divestiture in
this instance.
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\29\ TC-023, TC-024, and TC-060; see also Amicus Brief from the
AIDS Healthcare Foundation, Dkt. 50-1.
\30\ See ``WellCare 2011 Annual Report'', available at https://ir.wellcare.com/file/4091918/Index?KeyFile=1500074253.
\31\ See ``WellCare Corporate Overview'', available at https://www.wellcare.com/en/Corporate/Company-Overview (last visited
February 13, 2019).
\32\ See ``WellCare Corporate Management Team'', available at
https://www.wellcare.com/Corporate/Management-Team (last visited
February 13, 2019).
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4. The remedy does not create new structural concerns in the markets
for individual PDPs.
The AMA incorrectly argues that, because WellCare and Aetna both
compete in all 34 Medicare regions, the divestiture itself creates
competitive concerns simply by reducing the number of competitors in
every region.\33\ The AMA further alleges that, in seven regions, the
divestiture ``would potentially raise significant competitive concerns
[that] often warrant scrutiny'' because it exceeds certain Herfindahl-
Hirschman Index (``HHI'') thresholds in the Horizontal Merger
Guidelines.\34\
---------------------------------------------------------------------------
\33\ TC-030 at 6-7.
\34\ Id.
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HHIs are a commonly accepted measure of market concentration and
are calculated by squaring the market share of each firm competing in
the market and then summing the resulting numbers.\35\ The U.S.
Department of Justice, consistent with the Federal Trade Commission,
generally considers markets in which the HHI is between 1,500 and 2,500
points to be moderately concentrated, and considers markets in which
the HHI is in excess of 2,500 points to be highly concentrated.\36\
Transactions that increase the HHI by more than 100 points in
moderately concentrated markets or between 100 and 200 points in highly
concentrated markets ``potentially raise significant competitive
concerns and often warrant scrutiny.'' \37\ Transactions that increase
the HHI by more than 200 points in highly concentrated markets are
``presumed to be likely to enhance market power.'' \38\
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\35\ For example, for a market consisting of four firms with
shares of 30, 30, 20, and 20 percent, the HHI is 2,600 (30\2\ +
30\2\ + 20\2\ + 20\2\ = 2,600).
\36\ See U.S. Department of Justice & FTC, Horizontal Merger
Guidelines Sec. 5.3 (2010), available at https://www.justice.gov/atr/file/810276/download.
\37\ Id.
\38\ Id.
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In this case, although some regions fall into the category of
``potentially'' raising concerns under the Horizontal Merger Guidelines
after the divestiture, no regions are above the threshold for
``presumed'' concerns. Moreover, as described in the 2010 Horizontal
Merger Guidelines, while the United States does use HHIs and other
concentration statistics, such as the number of firms in the market, as
an important part of its investigative toolkit, ``[t]he purpose of
these thresholds is not to provide a rigid screen to separate
competitively benign mergers from anticompetitive ones . . . [r]ather,
they provide one way to identify some mergers unlikely to raise
competitive concerns and some others for which it is particularly
important to examine whether other competitive factors confirm,
reinforce, or counteract the potentially harmful effects of increased
concentration.'' \39\ Consistent with these principles, the United
States considered the strength of WellCare, Aetna, and their
competitors in all 34 PDP regions. The combined market share of Aetna's
and WellCare's individual PDP businesses does not exceed 25 percent in
any region. The United States determined that the combination of
Aetna's and WellCare's PDP business was not likely to substantially
lessen competition, in part due to the presence of other significant
competitors--including CVS's SilverScript product--in every market.
---------------------------------------------------------------------------
\39\ Id.
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5. The licensing provisions related to the Aetna brand protect
WellCare's ability to compete using the divested assets.
Under Section IV.I. of the proposed Final Judgment, Aetna is
required to license the Aetna brand to WellCare for use with the
divested business only for 2019. For 2020, Section IV.J. of the
proposed Final Judgment prohibits CVS from using the Aetna brand for
the sale of individual PDPs. Misunderstanding these provisions, the
joint comment from Consumer Action and U.S. PIRG raises concerns that
WellCare's one-year license to the Aetna brand fails to create an
incentive to properly invest in the Aetna brand name.\40\ The proposed
Final Judgment, however, is not meant to give WellCare a long-term
incentive to invest in the Aetna brand name. Rather, these provisions
give WellCare a two-year opportunity to establish its relationship with
the customers of the divested plans without a competing Aetna-branded
individual PDP plan. Given that, as previously explained, the
divestiture improves WellCare's established ability to compete for PDP
customers, these provisions further enhance the effectiveness of the
proposed Final Judgment.
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\40\ TC-023, TC-024; see also TC-003.
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6. The sales price does not cast doubt on WellCare's intention to
compete.
Several commenters raise misplaced concerns related to the price
paid by WellCare.\41\ For example, the joint comment from Consumer
Action and U.S. PIRG estimates the divestiture purchase price to be $45
per life and then claims--without evidence--that this ``seems like a
very cheap price.'' \42\ In some cases, a low purchase price may raise
concerns whether a proposed divestiture buyer will be a successful
competitor.\43\ As described in the 2004 Policy Guide to Merger
Remedies, ``the purchase price will not be approved if it clearly
indicates that the purchaser is unable or unwilling to compete in the
relevant market.'' \44\ The Policy Guide also states, however, that ``a
successful divestiture does not depend on the price paid for the
assets.'' \45\ Rather, a low price ``may simply mean the purchaser is
getting a bargain'' and ``if the Division has other sufficient
assurances that the proposed purchaser intends to compete in the
relevant market, the Division will not require . . . [a certain]
price.'' \46\
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\41\ TC-003, TC-023, TC-024, and TC-060.
\42\ TC-023 at 5, TC-024 at 7.
\43\ See, e.g., United States v. Aetna, Inc., 240 F. Supp. 3d 1,
72 (D.D.C. 2017) (citing to an ``extremely low'' purchase price as
evidence that the divestiture buyer was not likely to be able to
replace the competition lost by the merger).
\44\ Antitrust Division Policy Guide to Merger Remedies, October
2004, at 33 available at https://www.justice.gov/sites/default/files/atr/legacy/2011/06/16/205108.pdf.
\45\ Id.
\46\ Id. at 34.
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[[Page 5474]]
In this case, the Antitrust Division has those assurances. The
United States thoroughly vetted WellCare, which has offered individual
PDPs since the program's inception in 2006 and has recently experienced
strong organic growth.\47\ The United States interviewed WellCare's
executives, reviewed its business plans, and discussed WellCare with
relevant third parties. Based on these efforts, the United States
believes that WellCare will continue to compete in individual PDPs, a
market it has participated in for over a decade. The commenters do not
provide any evidence that their estimated purchase price undermines
this conclusion.
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\47\ See CMS Monthly Enrollment by CPSC for January 2019,
available at https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports/MCRAdvPartDEnrolData/Monthly-Enrollment-by-Contract-Plan-State-County-Items/Monthly-Enrollment-by-CPSC-2019-01.html?DLPage=1&DLEntries=10&DLSort=1&DLSortDir=descending.
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B. Comments Related to the Vertical Aspects of CVS's Acquisition of
Aetna
Asking the Court to go outside the permissible scope of review
under the Tunney Act, commenters also raise vertical concerns about the
merger combining CVS's pharmacy and PBM businesses with Aetna's health
insurance businesses, alleging that the merger will enable CVS to use
its assets to harm competitors. CVS can be viewed as competing at three
different levels of the healthcare industry: (1) the sale of drugs
through channels such as retail, mail order, and long-term care
pharmacies; (2) the provision of PBM services that are offered to
insurers, including the negotiation of rates with pharmaceutical
manufacturers and the negotiation of coverage networks with pharmacies;
and (3) the sale of various types of insurance, including individual
PDPs. CVS competes at all three of these levels through its branded
retail, long-term care, and other pharmacies; through its PBM,
Caremark; and through SilverScript, its individual PDP. Aetna competes
with SilverScript at the third level, and offers additional types of
insurance, but does not offer stand-alone PBM services or own any
retail pharmacies of its own.
Recognizing that CVS and Aetna do not compete against each other
either at the retail pharmacy level or the PBM level, commenters
nonetheless raise two categories of vertical concerns relating to the
merger: input foreclosure and customer foreclosure concerns, which are
explained below. Commenters also raise vertical concerns about CVS's
common ownership of its retail pharmacies and Caremark, its PBM, which
CVS owned long before it sought to acquire Aetna and is unrelated to
the current merger.
The United States investigated the potential for vertical harms
from the merger by obtaining and reviewing documents as well as
interviewing industry participants. For the reasons outlined below, the
United States concluded that vertical harms were unlikely to occur and
did not allege any harm related to vertical concerns in its Complaint.
The vertical concerns therefore are outside the scope of this Tunney
Act proceeding. See United States' December 14, 2018 Response to Order
to Show Cause, Dkt. #32, at 3-7. Responding to the AAI's comment that
there are benefits to transparency, the United States nonetheless
describes the commenters' concerns and responds below.
1. Input foreclosure is unlikely to occur and is beyond the scope of
the Complaint.
Although several comments raise the possibility that the merged
firm will harm competition in the sale of health insurance by raising
the cost of important services or products that CVS provides to
insurers that compete with Aetna, which is known as input foreclosure,
the United States considered this possibility and determined that input
foreclosure is unlikely to be profitable for CVS. In particular,
commenters argue that CVS will deny or restrict health insurance
rivals' access to inputs at two different levels of the supply chain:
First, commenters \48\ allege that the company will not make its
pharmacies available to competing health plans or will otherwise
disadvantage rival plans by raising pharmacy costs. Second, commenters
\49\ allege that Caremark will not make its PBM services available to
competing health plans or will raise the prices for its PBM services to
rival plans.\50\ Neither is likely to occur.
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\48\ TC-001, TC-002, TC-003, TC-023, and TC-024; see also Amicus
Brief from the AIDS Healthcare Foundation, Dkt. # 50-1.
\49\ TC-001, TC-002, TC-003, TC-023, TC-024, TC-048, TC-054, and
TC-057.
\50\ Additionally, some commenters also allege that CVS is
foreclosing 340B administrators from its retail pharmacies. See TC-
066, TC-068. 340B administrators offer services to assemble and
administer pharmacy networks that provide rebates to qualified
hospitals. CVS competes with these administrators through a
subsidiary called Wellpartner. These commenters allege that CVS does
not allow its pharmacies to participate in 340B networks unless
Wellpartner is selected as the hospital's 340B administrator, which
would be a form of input foreclosure. CVS's acquisition of Aetna
does not relate to the 340B market or affect shares in that market.
In part for this reason, the United States did not allege
anticompetitive effects from the merger related to CVS or
Wellpartner's practice