Determination and Declaration Regarding Emergency Use of Doxycycline Hyclate Tablets Accompanied by Emergency Use Information, 58242-58243 [E8-23544]
Download as PDF
58242
Federal Register / Vol. 73, No. 194 / Monday, October 6, 2008 / Notices
a federal declaration in support of an
emergency use authorization under
This first day of October, 2008.
Michael O. Leavitt,
Secretary of Health and Human Services.
section 564 of the FDCA unless such
declaration specifies otherwise.
APPENDIX I—LIST OF U.S. GOVERNMENT CONTRACTS
Contract
Manufacturer
Covered countermeasure
HHSO100200500007C ........................
HHSO100200500006C ........................
HHSO100200600019C ........................
HHSO100200700037C ........................
W9113M–04–D–0002 ..........................
DAMD 17–97–D–00003 .......................
Cangene .............................................
HGS ...................................................
Emergent Biodefense Operations ......
Emergent Biodefense Operations ......
BioPort (Emergent Biosolutions) ........
BioPort (Emergent Biosolutions) ........
HHSN 272200700035C .......................
HHSN 272200700033C .......................
HHSN 272200700034C .......................
NO1–A1–30052 ....................................
Elusys .................................................
Pharmathene ......................................
Emergent BioSolutions ......................
Avecia (Pharmathene) .......................
V797P–5777x .......................................
V797P–5977x .......................................
V797P–5941x .......................................
V797P–5883x .......................................
V797P–5669x .......................................
V797–DSNS–8002 ...............................
V797–DSNS–8002 ...............................
V797BPA0015 ......................................
V797P–5396x .......................................
V797P–5669x .......................................
V797P–1020x .......................................
V797P–5387x .......................................
Shering Corp. .....................................
Cobalt Pharmaceuticals .....................
Blu Pharmaceuticals ..........................
Pfizer, Inc ...........................................
Abraxis Bioscience, Inc ......................
Sandoz, Inc ........................................
Sandoz, Inc ........................................
Bedford Labs ......................................
Hospira ...............................................
Abraxis Bioscience, Inc ......................
McKesson ..........................................
Johnson and Johnson Healthcare .....
Anthrax immune globulin—AIG ..............................
Anthrax monoclonal antibody-ABThrax .................
BioThrax (Anthrax Vaccine Adsorbed, AVA) .........
BioThrax (Anthrax Vaccine Adsorbed, AVA) .........
BioThrax (Anthrax Vaccine Adsorbed, AVA) .........
BioThrax (Anthrax Vaccine Adsorbed, AVA) Shipping.
Anthrax monoclonal antibody—ETI–204 ...............
Anthrax monoclonal antibody—Valortim ................
Anthrax immune globulin—AIG ..............................
Recombinant protective antigen (rPA) anthrax
vaccine.
Cipro 250mg/5ml; 100ml suspension ....................
Cipro 500mg tablets ...............................................
Doxycycline 100mg tablets ....................................
Doxycycline 25mg/5ml suspension 60ml ...............
Doxycycline 100mg vial IV .....................................
Amoxicillin 500mg capsules ...................................
Amoxicillin 400mg/5ml; 100ml suspension ............
Rifampin 600mg vial IV ..........................................
Clindamycin 150mg/ml 6ml vial IV .........................
Vancomycin 1 g vial IV ..........................................
Penicillin GK 20 million unit vial IV ........................
Levofloxacin 5mg/ml 150ml bag IV ........................
PL 85–804
coverage*
No.
No.
Yes.
No.
Yes.
Yes.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
No.
* Status of indemnification coverage under P.L. 85–804 (An Act to authorize the making, amendment and modification of contracts to facilitate
the national defense.)
[FR Doc. E8–23547 Filed 10–1–08; 4:15 pm]
BILLING CODE 4150–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Determination and Declaration
Regarding Emergency Use of
Doxycycline Hyclate Tablets
Accompanied by Emergency Use
Information
AGENCY:
Office of the Secretary (OS),
HHS.
jlentini on PROD1PC65 with NOTICES
ACTION:
Notice.
SUMMARY: The Secretary of the
Department of Health and Human
Services (HHS) is issuing this notice
pursuant to section 564(b)(4) of the
Federal Food, Drug, and Cosmetic Act
(FFDCA), 21 U.S.C. 360bbb–3(b)(4), to
justify the emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information, contained in emergency
kits for eligible United States Postal
Service (USPS) Cities Readiness
Initiative (CRI) participants and their
household members in advance of a
potential attack involving Bacillus
anthracis. Bacillus anthracis is a
VerDate Aug<31>2005
17:44 Oct 03, 2008
Jkt 217001
biological agent known to cause
anthrax. The Secretary, HHS, provides
notice of the determination of the
Secretary of Homeland Security on
September 23, 2008 that there is a
significant potential for a domestic
emergency involving a heightened risk
of attack with a specified biological,
chemical, radiological, or nuclear agent
or agents—in this case, Bacillus
anthracis, although there is no current
domestic emergency involving anthrax,
no current heightened risk of an anthrax
attack, and no credible information
indicating an imminent threat of an
attack involving Bacillus anthracis. The
Secretary also provides notice that, on
the basis of such determination, he has
declared an emergency justifying the
authorization of emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information subject to the terms of any
authorization issued by the Food and
Drug Commissioner under 21 U.S.C.
360bbb–3(a).
DATES: This Notice and referenced HHS
declaration are effective as of October 1,
2008.
FOR FURTHER INFORMATION CONTACT:
RADM W.C. Vanderwagen, M.D.,
Assistant Secretary for Preparedness
and Response, Office of the Secretary,
Department of Health and Human
PO 00000
Frm 00133
Fmt 4703
Sfmt 4703
Services, 200 Independence Avenue,
SW., Washington, DC 20201, Telephone
(202) 205–2882 (this is not a toll free
number).
SUPPLEMENTARY INFORMATION:
I. Background
The CRI, begun in 2004, is a federally
supported effort to prepare 72 major
U.S. metropolitan areas to effectively
respond to a large-scale bioterrorist
event by dispensing antibiotics to their
entire identified population within 48
hours of the decision to do so. Over the
past several years, HHS and the USPS
have developed and tested in three U.S.
cities—Seattle, Philadelphia and
Boston—the ability of letter carriers to
quickly deliver door-to-door a few days’
worth of antibiotics to residential
addresses. This quick-strike capability is
intended to buy time for State and local
public health authorities to set up
points of dispensing for further
provision of antibiotics across the
community, as needed.
Under Section 564 of the FFDCA, the
Secretary of Homeland Security may
determine that there is a domestic
emergency, or a significant potential for
a domestic emergency, involving a
heightened risk of attack with a
specified biological chemical,
radiological or nuclear agent or agents.
E:\FR\FM\06OCN1.SGM
06OCN1
jlentini on PROD1PC65 with NOTICES
Federal Register / Vol. 73, No. 194 / Monday, October 6, 2008 / Notices
Based on such a determination, the
Secretary of Health and Human Services
may declare an emergency that justifies
the authorization of a product that is not
otherwise approved, licensed or cleared
for commercial use (‘‘unapproved
product’’) or is not approved, licensed,
or cleared for a particular use
(‘‘unapproved use of an approved
product.’’). Following that declaration,
the Commissioner of the Food and Drug
Administration (FDA) may issue an
Emergency Use Authorization (EUA).
The Biomedical Advanced Research
and Development Authority (BARDA) of
the HHS Office of the Assistant
Secretary for Preparedness and
Response (ASPR) has requested that
FDA issue an EUA for doxycycline
hyclate tablets accompanied by
emergency use information for use by
eligible USPS participants in the CRI
and their household members.
Doxycyline hyclate tablets are approved
by the FDA for the post-exposure
prophylaxis of anthrax. However, the
doxycycline hyclate tablets for which
BARDA seeks an EUA would be
accompanied by emergency use
information that is not included in any
of the approved applications for
doxyclycline hyclate tablets. For this
reason, an EUA is necessary. The
September 23, 2008 determination by
the Secretary of Homeland Security that
there is a significant potential for a
domestic emergency, involving a
heightened risk of attack with a
specified biological, chemical,
radiological, or nuclear agent or
agents—in this case, Bacillus anthracis,
and the October 1, 2008 declaration by
the Secretary of Health and Human
Services based on that determination
that there is an emergency justifying the
authorization of emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information, enables the FDA
Commissioner to issue an EUA for
doxycyline hyclate tablet emergency
kits under section 564(a) of the FFDCA,
21 U.S.C. 360bbb–3(a).
With issuance of the EUA, eligible
letter carriers participating in the CRI
may receive the doxycycline hyclate
tablet emergency kits, if not medically
contraindicated, for future use by them
and other members of their households
during an anthrax emergency, subject to
the terms of the authorization. The
antibiotics and accompanying
information may help protect these
letter carriers and household members
against contracting anthrax if, following
an outdoor anthrax attack, the USPS is
called upon to deliver the same or
similar antibiotics to homes across their
community where people may have
VerDate Aug<31>2005
17:44 Oct 03, 2008
Jkt 217001
been exposed to Bacillus anthracis. In
an anthrax attack, time is of the essence
in preventing illness and death by
getting antibiotics to people who may
have been exposed. By providing
advance protection to letter carriers who
willingly put themselves at risk by
delivering antibiotics in an affected
community, the unique capabilities of
the USPS may be used to get antibiotics
to those who need them quickly.
The USPS initiative and EUA are one
part of the Federal Government’s
strategy to encourage preparedness at all
levels of government to enable the
nation to respond effectively in the
event of an anthrax emergency.
II. Determination of the Secretary of
Homeland Security
On September 23, 2008, pursuant to
section 564(b)(1)(A) of the FFDCA, 21
U.S.C. 360bbb–3(b)(1)(A), the Secretary
of Homeland Security determined that
there is a significant potential for a
domestic emergency, involving a
heightened risk of attack with a
specified biological, chemical,
radiological, or nuclear agent or
agents—in this case, Bacillus anthracis.
The Secretary of Homeland Security
made this determination in a September
23, 2008 memorandum addressed to the
Secretary of Health and Human
Services. In that memorandum, the
Secretary of Homeland Security stated
that there is not currently a domestic
emergency involving anthrax, there is
not currently a heightened risk of an
anthrax attack, and his Department has
no credible information indicating an
imminent threat of an attack involving
Bacillus anthracis.
The Secretary of Homeland Security
determined that there is a significant
potential for a domestic emergency,
involving a heightened risk of attack
with Bacillus anthracis, on two bases:
(1) The Department of Homeland
Security has already found that an
anthrax attack poses a material threat to
the United States population sufficient
to affect national security, which allows
the Secretary to conclude that there is
a non-negligible possibility that a
heightened risk of attack will arise. The
finding that an anthrax attack poses a
material threat to the United States
population sufficient to affect national
security was made on January 20, 2004
regarding anthrax, and on September 22,
2006 regarding multi-drug resistant
Bacillus anthracis, pursuant to section
319F–2(c)(2) of the Public Health
Service (PHS) Act, 42 U.S.C. 247d–
6b(c)(2). (2) Were the government to
determine in the future that there is a
heightened risk of an anthrax attack—if,
for example, there were credible
PO 00000
Frm 00134
Fmt 4703
Sfmt 4703
58243
information about an imminent threat of
such an attack—that would almost
certainly result in a domestic
emergency. That is so, among other
important reasons, because those
exposed to Bacillus anthracis need to
take appropriate antimicrobials rapidly
after exposure to avoid contracting
anthrax and because of the significant
challenges to rapidly delivering such
antimicrobials to those at risk in an
anthrax emergency.
Given his determination that there is
a significant potential for a domestic
emergency, the Secretary of Homeland
Security also urged the Secretary of
Health and Human Services to employ
all relevant emergency powers under
section 564 of the FFDCA to ensure
distribution of pre-need
countermeasures that may be effective
in preventing the contracting of anthrax
by people in the delivery chain, such as
USPS workers; first responders,
including law enforcement; to essential
government and non-government
workers; and to the general public.
III. Declaration of the Secretary of
Health and Human Services
On September 23, 2008, the Secretary
of the Department of Homeland Security
determined that there is a significant
potential for a domestic emergency,
involving a heightened risk of attack
with a specified biological, chemical,
radiological, or nuclear agent or
agents—in this case, Bacillus anthracis.
Pursuant to section 564(b) of the Federal
Food, Drug and Cosmetic Act, 21 U.S.C.
360bbb–3(b), and on the basis of such
determination, on October 1, 2008, I
declared an emergency justifying the
authorization of the emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information subject to the terms of any
authorization issued under 21 U.S.C.
360bbb–3(a).
Dated: October 1, 2008.
Michael O. Leavitt,
Secretary.
[FR Doc. E8–23544 Filed 10–1–08; 4:15 pm]
BILLING CODE 4150–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Committee on Vital and Health
Statistics: Meeting
Pursuant to the Federal Advisory
Committee Act, the Department of
Health and Human Services (HHS)
announces the following advisory
committee meeting.
E:\FR\FM\06OCN1.SGM
06OCN1
Agencies
[Federal Register Volume 73, Number 194 (Monday, October 6, 2008)]
[Notices]
[Pages 58242-58243]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-23544]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Determination and Declaration Regarding Emergency Use of
Doxycycline Hyclate Tablets Accompanied by Emergency Use Information
AGENCY: Office of the Secretary (OS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Secretary of the Department of Health and Human Services
(HHS) is issuing this notice pursuant to section 564(b)(4) of the
Federal Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 360bbb-3(b)(4),
to justify the emergency use of doxycycline hyclate tablets accompanied
by emergency use information, contained in emergency kits for eligible
United States Postal Service (USPS) Cities Readiness Initiative (CRI)
participants and their household members in advance of a potential
attack involving Bacillus anthracis. Bacillus anthracis is a biological
agent known to cause anthrax. The Secretary, HHS, provides notice of
the determination of the Secretary of Homeland Security on September
23, 2008 that there is a significant potential for a domestic emergency
involving a heightened risk of attack with a specified biological,
chemical, radiological, or nuclear agent or agents--in this case,
Bacillus anthracis, although there is no current domestic emergency
involving anthrax, no current heightened risk of an anthrax attack, and
no credible information indicating an imminent threat of an attack
involving Bacillus anthracis. The Secretary also provides notice that,
on the basis of such determination, he has declared an emergency
justifying the authorization of emergency use of doxycycline hyclate
tablets accompanied by emergency use information subject to the terms
of any authorization issued by the Food and Drug Commissioner under 21
U.S.C. 360bbb-3(a).
DATES: This Notice and referenced HHS declaration are effective as of
October 1, 2008.
FOR FURTHER INFORMATION CONTACT: RADM W.C. Vanderwagen, M.D., Assistant
Secretary for Preparedness and Response, Office of the Secretary,
Department of Health and Human Services, 200 Independence Avenue, SW.,
Washington, DC 20201, Telephone (202) 205-2882 (this is not a toll free
number).
SUPPLEMENTARY INFORMATION:
I. Background
The CRI, begun in 2004, is a federally supported effort to prepare
72 major U.S. metropolitan areas to effectively respond to a large-
scale bioterrorist event by dispensing antibiotics to their entire
identified population within 48 hours of the decision to do so. Over
the past several years, HHS and the USPS have developed and tested in
three U.S. cities--Seattle, Philadelphia and Boston--the ability of
letter carriers to quickly deliver door-to-door a few days' worth of
antibiotics to residential addresses. This quick-strike capability is
intended to buy time for State and local public health authorities to
set up points of dispensing for further provision of antibiotics across
the community, as needed.
Under Section 564 of the FFDCA, the Secretary of Homeland Security
may determine that there is a domestic emergency, or a significant
potential for a domestic emergency, involving a heightened risk of
attack with a specified biological chemical, radiological or nuclear
agent or agents.
[[Page 58243]]
Based on such a determination, the Secretary of Health and Human
Services may declare an emergency that justifies the authorization of a
product that is not otherwise approved, licensed or cleared for
commercial use (``unapproved product'') or is not approved, licensed,
or cleared for a particular use (``unapproved use of an approved
product.''). Following that declaration, the Commissioner of the Food
and Drug Administration (FDA) may issue an Emergency Use Authorization
(EUA).
The Biomedical Advanced Research and Development Authority (BARDA)
of the HHS Office of the Assistant Secretary for Preparedness and
Response (ASPR) has requested that FDA issue an EUA for doxycycline
hyclate tablets accompanied by emergency use information for use by
eligible USPS participants in the CRI and their household members.
Doxycyline hyclate tablets are approved by the FDA for the post-
exposure prophylaxis of anthrax. However, the doxycycline hyclate
tablets for which BARDA seeks an EUA would be accompanied by emergency
use information that is not included in any of the approved
applications for doxyclycline hyclate tablets. For this reason, an EUA
is necessary. The September 23, 2008 determination by the Secretary of
Homeland Security that there is a significant potential for a domestic
emergency, involving a heightened risk of attack with a specified
biological, chemical, radiological, or nuclear agent or agents--in this
case, Bacillus anthracis, and the October 1, 2008 declaration by the
Secretary of Health and Human Services based on that determination that
there is an emergency justifying the authorization of emergency use of
doxycycline hyclate tablets accompanied by emergency use information,
enables the FDA Commissioner to issue an EUA for doxycyline hyclate
tablet emergency kits under section 564(a) of the FFDCA, 21 U.S.C.
360bbb-3(a).
With issuance of the EUA, eligible letter carriers participating in
the CRI may receive the doxycycline hyclate tablet emergency kits, if
not medically contraindicated, for future use by them and other members
of their households during an anthrax emergency, subject to the terms
of the authorization. The antibiotics and accompanying information may
help protect these letter carriers and household members against
contracting anthrax if, following an outdoor anthrax attack, the USPS
is called upon to deliver the same or similar antibiotics to homes
across their community where people may have been exposed to Bacillus
anthracis. In an anthrax attack, time is of the essence in preventing
illness and death by getting antibiotics to people who may have been
exposed. By providing advance protection to letter carriers who
willingly put themselves at risk by delivering antibiotics in an
affected community, the unique capabilities of the USPS may be used to
get antibiotics to those who need them quickly.
The USPS initiative and EUA are one part of the Federal
Government's strategy to encourage preparedness at all levels of
government to enable the nation to respond effectively in the event of
an anthrax emergency.
II. Determination of the Secretary of Homeland Security
On September 23, 2008, pursuant to section 564(b)(1)(A) of the
FFDCA, 21 U.S.C. 360bbb-3(b)(1)(A), the Secretary of Homeland Security
determined that there is a significant potential for a domestic
emergency, involving a heightened risk of attack with a specified
biological, chemical, radiological, or nuclear agent or agents--in this
case, Bacillus anthracis. The Secretary of Homeland Security made this
determination in a September 23, 2008 memorandum addressed to the
Secretary of Health and Human Services. In that memorandum, the
Secretary of Homeland Security stated that there is not currently a
domestic emergency involving anthrax, there is not currently a
heightened risk of an anthrax attack, and his Department has no
credible information indicating an imminent threat of an attack
involving Bacillus anthracis.
The Secretary of Homeland Security determined that there is a
significant potential for a domestic emergency, involving a heightened
risk of attack with Bacillus anthracis, on two bases: (1) The
Department of Homeland Security has already found that an anthrax
attack poses a material threat to the United States population
sufficient to affect national security, which allows the Secretary to
conclude that there is a non-negligible possibility that a heightened
risk of attack will arise. The finding that an anthrax attack poses a
material threat to the United States population sufficient to affect
national security was made on January 20, 2004 regarding anthrax, and
on September 22, 2006 regarding multi-drug resistant Bacillus
anthracis, pursuant to section 319F-2(c)(2) of the Public Health
Service (PHS) Act, 42 U.S.C. 247d-6b(c)(2). (2) Were the government to
determine in the future that there is a heightened risk of an anthrax
attack--if, for example, there were credible information about an
imminent threat of such an attack--that would almost certainly result
in a domestic emergency. That is so, among other important reasons,
because those exposed to Bacillus anthracis need to take appropriate
antimicrobials rapidly after exposure to avoid contracting anthrax and
because of the significant challenges to rapidly delivering such
antimicrobials to those at risk in an anthrax emergency.
Given his determination that there is a significant potential for a
domestic emergency, the Secretary of Homeland Security also urged the
Secretary of Health and Human Services to employ all relevant emergency
powers under section 564 of the FFDCA to ensure distribution of pre-
need countermeasures that may be effective in preventing the
contracting of anthrax by people in the delivery chain, such as USPS
workers; first responders, including law enforcement; to essential
government and non-government workers; and to the general public.
III. Declaration of the Secretary of Health and Human Services
On September 23, 2008, the Secretary of the Department of Homeland
Security determined that there is a significant potential for a
domestic emergency, involving a heightened risk of attack with a
specified biological, chemical, radiological, or nuclear agent or
agents--in this case, Bacillus anthracis. Pursuant to section 564(b) of
the Federal Food, Drug and Cosmetic Act, 21 U.S.C. 360bbb-3(b), and on
the basis of such determination, on October 1, 2008, I declared an
emergency justifying the authorization of the emergency use of
doxycycline hyclate tablets accompanied by emergency use information
subject to the terms of any authorization issued under 21 U.S.C.
360bbb-3(a).
Dated: October 1, 2008.
Michael O. Leavitt,
Secretary.
[FR Doc. E8-23544 Filed 10-1-08; 4:15 pm]
BILLING CODE 4150-37-P