Certain Photodynamic Therapy Systems, Components Thereof, and Pharmaceutical Products Used in Combination With the Same; Notice of Commission Determination Not To Review an Initial Determination Granting in Part Complainant's Motion To Amend the Complaint and Notice of Investigation, 92976 [2024-27568]
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92976
Federal Register / Vol. 89, No. 227 / Monday, November 25, 2024 / Notices
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U.S.C. 3004 and the implementing
regulations, 43 CFR 10.9.
Dated: November 18, 2024.
Melanie O’Brien,
Manager, National NAGPRA Program.
[FR Doc. 2024–27514 Filed 11–22–24; 8:45 am]
BILLING CODE 4312–52–P
INTERNATIONAL TRADE
COMMISSION
[Investigation No. 337–TA–1411]
Certain Photodynamic Therapy
Systems, Components Thereof, and
Pharmaceutical Products Used in
Combination With the Same; Notice of
Commission Determination Not To
Review an Initial Determination
Granting in Part Complainant’s Motion
To Amend the Complaint and Notice of
Investigation
U.S. International Trade
Commission.
ACTION: Notice.
AGENCY:
Notice is hereby given that
the U.S. International Trade
Commission has determined not to
review an initial determination (‘‘ID’’)
(Order No. 8) of the presiding
administrative law judge (‘‘ALJ’’) issued
in the above-captioned investigation,
granting in part complainant’s motion to
amend the complaint and notice of
investigation (‘‘NOI’’) to add
infringement allegations as to claims 17
and 18 of U.S. Patent No. 11,446,512
(‘‘the ’512 patent’’).
FOR FURTHER INFORMATION CONTACT:
Richard P. Hadorn, Esq., Office of the
General Counsel, U.S. International
Trade Commission, 500 E Street SW,
Washington, DC 20436, telephone (202)
205–3179. Copies of non-confidential
documents filed in connection with this
investigation may be viewed on the
khammond on DSK9W7S144PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:29 Nov 22, 2024
Jkt 265001
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov. For help
accessing EDIS, please email
EDIS3Help@usitc.gov. General
information concerning the Commission
may also be obtained by accessing its
internet server at https://www.usitc.gov.
Hearing-impaired persons are advised
that information on this matter can be
obtained by contacting the
Commission’s TDD terminal, telephone
(202) 205–1810.
SUPPLEMENTARY INFORMATION: The
Commission instituted this investigation
on August 1, 2024, based on a complaint
filed by Sun Pharmaceutical Industries,
Inc. (‘‘Sun Pharma’’) of Princeton, New
Jersey. 89 FR 62790 (Aug. 1, 2024). The
complaint, as supplemented, alleges
violations of section 337 of the Tariff
Act of 1930, as amended, 19 U.S.C.
1337, based on the importation into the
United States, the sale for importation,
and the sale within the United States
after importation of certain
photodynamic therapy systems,
components thereof, and
pharmaceutical products used in
combination with the same by reason of
infringement of certain claims of the
’512 patent and U.S. Patent No.
11,697,028 (‘‘the ’028 patent’’). Id. The
complaint further alleges that a
domestic industry exists or is in the
process of being established. Id. The
notice of investigation names four
respondents: (1) Biofrontera Inc. of
Woburn, Massachusetts; (2) Biofrontera
Pharma GmbH of Leverkusen, Germany;
(3) Biofrontera Bioscience GmbH of
Leverkusen, Germany; and (4)
Biofrontera AG of Leverkusen, Germany
(collectively, ‘‘Biofrontera’’). Id. The
Office of Unfair Import Investigations is
not a party to this investigation. Id.
On October 7, 2024, Sun Pharma filed
a motion to amend the complaint and
NOI to add infringement allegations as
to claims 9, 11, 17, and 18 of the ’512
patent and claims 10 and 12 of the ’028
patent. On October 17, 2024, Biofrontera
filed a response opposing-in-part the
motion. Specifically, Biofrontera did not
oppose the motion with respect to
adding infringement allegations as to
claims 17 and 18 of the ’512 patent, but
opposed the remainder of the motion.
On October 22, 2024, the ALJ issued
the subject ID granting the motion in
part. The ID finds that, in accordance
with Commission Rule 210.14(b) (19
CFR 210.14(b)), good cause exists for
amending the complaint and NOI to add
infringement allegations as to claims 17
and 18 of the ’512 patent, noting that
‘‘Biofrontera agrees that Sun Pharma’s
allegations with respect to these claims
are based on information obtained
PO 00000
Frm 00093
Fmt 4703
Sfmt 4703
through discovery.’’ ID at 3. The ALJ,
however, found that Sun Pharma has
not shown the requisite good cause to
amend the complaint and NOI to add
infringement allegations as to claims 9
and 11 of the ’512 patent and claims 10
and 12 of the ’028 patent because ‘‘Sun
Pharma failed to demonstrate why it
was unable to bring the allegations [of
those claims] in the complaint.’’ Id. at
3–5. No petitions for review of the
subject ID were filed.
The Commission has determined not
to review the subject ID. The complaint
and NOI are amended to add
infringement allegations as to claims 17
and 18 of the ’512 patent.
The Commission vote for this
determination took place on November
20, 2024.
The authority for the Commission’s
determination is contained in section
337 of the Tariff Act of 1930, as
amended (19 U.S.C. 1337), and in part
210 of the Commission’s Rules of
Practice and Procedure (19 CFR part
210).
By order of the Commission.
Issued: November 20, 2024.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2024–27568 Filed 11–22–24; 8:45 am]
BILLING CODE 7020–02–P
NUCLEAR REGULATORY
COMMISSION
[NRC–2024–0001]
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TIME AND DATE:
E:\FR\FM\25NON1.SGM
25NON1
Agencies
[Federal Register Volume 89, Number 227 (Monday, November 25, 2024)]
[Notices]
[Page 92976]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-27568]
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INTERNATIONAL TRADE COMMISSION
[Investigation No. 337-TA-1411]
Certain Photodynamic Therapy Systems, Components Thereof, and
Pharmaceutical Products Used in Combination With the Same; Notice of
Commission Determination Not To Review an Initial Determination
Granting in Part Complainant's Motion To Amend the Complaint and Notice
of Investigation
AGENCY: U.S. International Trade Commission.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the U.S. International Trade
Commission has determined not to review an initial determination
(``ID'') (Order No. 8) of the presiding administrative law judge
(``ALJ'') issued in the above-captioned investigation, granting in part
complainant's motion to amend the complaint and notice of investigation
(``NOI'') to add infringement allegations as to claims 17 and 18 of
U.S. Patent No. 11,446,512 (``the '512 patent'').
FOR FURTHER INFORMATION CONTACT: Richard P. Hadorn, Esq., Office of the
General Counsel, U.S. International Trade Commission, 500 E Street SW,
Washington, DC 20436, telephone (202) 205-3179. Copies of non-
confidential documents filed in connection with this investigation may
be viewed on the Commission's electronic docket (EDIS) at https://edis.usitc.gov. For help accessing EDIS, please email
[email protected]. General information concerning the Commission may
also be obtained by accessing its internet server at https://www.usitc.gov. Hearing-impaired persons are advised that information on
this matter can be obtained by contacting the Commission's TDD
terminal, telephone (202) 205-1810.
SUPPLEMENTARY INFORMATION: The Commission instituted this investigation
on August 1, 2024, based on a complaint filed by Sun Pharmaceutical
Industries, Inc. (``Sun Pharma'') of Princeton, New Jersey. 89 FR 62790
(Aug. 1, 2024). The complaint, as supplemented, alleges violations of
section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337,
based on the importation into the United States, the sale for
importation, and the sale within the United States after importation of
certain photodynamic therapy systems, components thereof, and
pharmaceutical products used in combination with the same by reason of
infringement of certain claims of the '512 patent and U.S. Patent No.
11,697,028 (``the '028 patent''). Id. The complaint further alleges
that a domestic industry exists or is in the process of being
established. Id. The notice of investigation names four respondents:
(1) Biofrontera Inc. of Woburn, Massachusetts; (2) Biofrontera Pharma
GmbH of Leverkusen, Germany; (3) Biofrontera Bioscience GmbH of
Leverkusen, Germany; and (4) Biofrontera AG of Leverkusen, Germany
(collectively, ``Biofrontera''). Id. The Office of Unfair Import
Investigations is not a party to this investigation. Id.
On October 7, 2024, Sun Pharma filed a motion to amend the
complaint and NOI to add infringement allegations as to claims 9, 11,
17, and 18 of the '512 patent and claims 10 and 12 of the '028 patent.
On October 17, 2024, Biofrontera filed a response opposing-in-part the
motion. Specifically, Biofrontera did not oppose the motion with
respect to adding infringement allegations as to claims 17 and 18 of
the '512 patent, but opposed the remainder of the motion.
On October 22, 2024, the ALJ issued the subject ID granting the
motion in part. The ID finds that, in accordance with Commission Rule
210.14(b) (19 CFR 210.14(b)), good cause exists for amending the
complaint and NOI to add infringement allegations as to claims 17 and
18 of the '512 patent, noting that ``Biofrontera agrees that Sun
Pharma's allegations with respect to these claims are based on
information obtained through discovery.'' ID at 3. The ALJ, however,
found that Sun Pharma has not shown the requisite good cause to amend
the complaint and NOI to add infringement allegations as to claims 9
and 11 of the '512 patent and claims 10 and 12 of the '028 patent
because ``Sun Pharma failed to demonstrate why it was unable to bring
the allegations [of those claims] in the complaint.'' Id. at 3-5. No
petitions for review of the subject ID were filed.
The Commission has determined not to review the subject ID. The
complaint and NOI are amended to add infringement allegations as to
claims 17 and 18 of the '512 patent.
The Commission vote for this determination took place on November
20, 2024.
The authority for the Commission's determination is contained in
section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and
in part 210 of the Commission's Rules of Practice and Procedure (19 CFR
part 210).
By order of the Commission.
Issued: November 20, 2024.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2024-27568 Filed 11-22-24; 8:45 am]
BILLING CODE 7020-02-P