[Federal Register: May 17, 2002 (Volume 67, Number 96)]
[Notices]
[Page 35114-35115]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr17my02-64]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Opportunity To Collaborate in the Evaluation of Topical
Microbicides To Reduce Sexual Transmission of Human Immunodeficiency
Virus (HIV)
AGENCY: Centers for Disease Control and Prevention, Department of
Health and Human Services (DHHS).
ACTION: Opportunities for collaboration for evaluation of topical
microbicides.
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The Centers for Disease Control and Prevention (CDC), National
Center for HIV, STD, and TB Prevention (NCHSTP), Division of HIV/AIDS
Prevention-Surveillance and Epidemiology (DHAP-SE), Epidemiology Branch
(EpiBr), announces an opportunity for collaboration to evaluate the
safety and preliminary efficacy of topical microbicides designed for
vaginal and/or rectal application to reduce HIV transmission. These
evaluations will include in-vitro assays, macaque studies, and phase I/
phase II trials in women and men.
SUMMARY: The Division of HIV/AIDS Prevention-Surveillance and
Epidemiology (DHAP-SE) of the National Center of HIV, STD, and TB
Prevention (NCHSTP) at the Centers for Disease Control and Prevention
(CDC) of the Department of Health and Human
[[Page 35115]]
Services (DHHS) seeks one or more pharmaceutical, biotechnical, or
other companies that hold a proprietary position on agents which may be
useful as microbicides to prevent sexual transmission of HIV infection.
The selected company and CDC will execute an Agreement under which the
company will provide a product for CDC to study the product's safety
and preliminary efficacy as a topical microbicide. Initial studies will
include in-vitro assays and may include macaque studies. Agents will be
selected for phase I and phase II trials in women and men based upon
data obtained in the CDC studies as well as other available published
and unpublished safety and efficacy data. Each collaboration would have
an expected duration of one (1) to five (5) years. The goals of the
collaboration include the timely development of data to further the
identification and commercialization of effective topical microbicides
and the rapid publication of research findings to increase the number
of HIV prevention technologies proven effective and available for use.
Confidential proposals, preferably 10 pages or less (excluding
appendices), are solicited from companies with patented or licensed
agents which have undergone sufficient preclinical testing to be
prepared to submit an Investigational New Drug (IND) application to the
FDA within six months of submitting the proposal.
DATES: This Notice will be open indefinitely.
ADDRESSES: Formal proposals should be submitted to Jeff Efird, MPA,
Epidemiology Branch, Division of HIV/AIDS Prevention--Surveillance and
Epidemiology, NCHSTP, CDC, 1600 Clifton Road, Mailstop E-45, Atlanta,
GA 30333; Phone: (direct) 404-639-6136, (office) 404-639-6130; Fax:
404-639-6127; e-mail: JLE1@cdc.gov. Scientific questions should be
addressed to Lisa A. Grohskopf, MD, MPH, Epidemiology Branch, Division
of HIV/AIDS Prevention -Surveillance and Epidemiology, NCHSTP, CDC,
1600 Clifton Road, Mailstop E-45, Atlanta, GA 30333; Phone: (direct)
404-639-6116, (office) 404-639-6146; Fax: 404-639-6127; e-mail:
lkg6@cdc.gov. Inquiries directed to ``Agreement'' documents related to
participation in this opportunity should be addressed to Thomas E.
O'Toole, MPH, Deputy Director, Technology Transfer Office, CDC, 1600
Clifton Road, Mailstop E-67, Atlanta, GA 30333; Phone: (direct) 404-
639-6270, (office) 404-639-6270; Fax: 404-639-6266; e-mail:
TEO1@cdc.gov
SUPPLEMENTARY INFORMATION:
Technology Available
One mission of the Epidemiology Branch (EpiBr) of DHAP-SE/NCHSTP is
to develop and evaluate biomedical interventions to reduce HIV
transmission. To this end, the EpiBr is establishing contracts to
conduct phase I and phase II trials of topical microbicides. EpiBr also
funds research in the Division of AIDS, STD, and TB Laboratory Research
(DASTLR) of the National Center for Infectious Diseases (NCID) at CDC
and with external laboratories to conduct macaque studies and in-vitro
studies in support of human microbicide trials. The goal of these
efforts is to provide scientific and technical expertise and key
resources for the evaluation of topical microbicides through late
preclinical, phase I and phase II safety and phase II efficacy clinical
trials.
Technology Sought
EpiBr now seeks potential collaborators having licensed or patented
agents for use as vaginal and/or rectal microbicides which:
(1) Have laboratory or animal model evidence of anti-HIV activity;
(2) Have been formulated for vaginal or rectal application;
(3) Are not entering phase III clinical trial in the next 12
months;
(4) Have sufficient preclinical data to submit an IND application
within approximately six months following submission of proposal; and
(5) Have manufacturing arrangements for production of clinical
trial-grade product (and applicator if necessary) under Good
Manufacturing Process (c-GMP) standards.
NCHSTP and Collaborator Responsibilities
The NCHSTP anticipates that its role may include, but not be
limited to, the following:
(1) Providing intellectual, scientific, and technical expertise and
experience to the research project;
(2) Planning and conducting preclinical (in-vitro and in-vivo)
research studies of the agent and interpreting results;
(3) Publishing research results;
(4) Depending on the results of these preclinical investigations,
NCHSTP may elect to conduct additional research with macaques to
evaluate safety and/or efficacy proof-of-concept; and
(5) Depending on the results of preclinical and/or macaque studies
and FDA approval, NCHSTP may elect to conduct phase I/II clinical
trials of the agent.
The NCHSTP anticipates that the role of the successful
collaborator(s) will include the following:
(1) Providing intellectual, scientific, and technical expertise and
experience to the research project;
(2) Participating in the planning of research studies,
interpretation of research results, and as appropriate, joint
publication of conclusions;
(3) Providing NCHSTP access to necessary proprietary technology
and/or data in support of the research activities; and
(4) Providing NCHSTP clinical grade (c-GMP) agent for use in
preclinical and clinical studies covered in this collaboration.
Other contributions may be necessary for particular proposals.
Selection Criteria
In addition to evidence of the ability to fulfill the roles
described above, proposals submitted for consideration should address,
as best as possible and to the extent relevant to the proposal, each of
the following:
(1) Data on the in-vitro anti-HIV activity of the agent;
(2) Animal and other data on the safety of the agent when applied
to mucosal surfaces;
(3) Data on the effects of the agent on vaginal and/or rectal
commensal microbial organisms; and
(4) Data on the in-vitro activity of the agent against other
sexually transmitted organisms.
Joseph R. Carter,
Associate Director for Management and Operations, Centers for Disease
Control and Prevention.
[FR Doc. 02-12353 Filed 5-16-02; 8:45 am]
BILLING CODE 4163-18-P