[Federal Register Volume 75, Number 109 (Tuesday, June 8, 2010)]
[Notices]
[Pages 32482-32483]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-13769]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0247]
Investigational New Drug Applications; Co-development of
Investigational Drugs
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; establishment of docket; request for comments.
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SUMMARY: The Food and Drug Administration (FDA) is establishing a
public docket to obtain input on methods to co-develop two or more
distinct investigational drugs intended to be used in combination to
treat a disease or condition. FDA is planning to develop guidance for
industry and other affected parties on the co-development of two or
more novel drugs intended to be used in combination (but not as not
fixed-dose combinations) and is seeking public input to identify the
affected parties' information needs concerning such co-development.
Accordingly, FDA is seeking comment on general methodologic and
regulatory issues that arise in various scenarios when co-developing
two or more investigational drugs intended to be used in combination.
FDA is also seeking comment on methodologic and regulatory issues when
co-developing two or more investigational drugs intended to be used in
combination for specific therapeutic areas, including oncology, anti-
infectives, seizure disorders, cardiovascular diseases, and any other
therapeutic category in which such co-development is likely to occur.
DATES: Submit either electronic or written comments by September 7,
2010.
ADDRESSES: Submit written comments to the Division of Dockets
Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane,
rm. 1061, Rockville, MD 20852. Submit electronic comments to http://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Colleen L. Locicero, Center for Drug
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, rm. 4200, Silver Spring, MD 20993-0002, 301-
796-2270.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is aware of growing interest in co-developing two or more
distinct, novel investigational drugs intended to be used in
combination to treat a disease or condition (but not as fixed-dose
combinations under 21 CFR 300.50). At a September 2009 conference co-
hosted by the ``Friends of Cancer Research'' in partnership with the
Engelberg Center for Health Care Reform at the Brookings Institution,
and supported by the American Society for Clinical Oncology (ASCO), the
American Association for Cancer Research (AACR) Susan G. Komen for the
Cure, and the Lance Armstrong Foundation (Brookings Conference), which
was attended by FDA scientists, there was considerable interest in
approaches to developing new oncology therapies intended to be used in
combination. In addition, on April 30, 2010, FDA held a public hearing
in accordance with part 15 (21 CFR part 15) devoted, in part, to
obtaining information about study designs and appropriate populations
for developing two or more novel, direct-acting antivirals intended to
be used in combination for the treatment of chronic hepatitis C. FDA is
also aware of efforts to try to develop two or more investigational
drugs intended to be used in combination to treat tuberculosis. FDA is
further aware of general uncertainty about the evidentiary requirements
and regulatory criteria applicable to such co-development efforts.
Accordingly, FDA is planning to develop generally applicable guidance
(not restricted to oncology or any other specific therapeutic category)
to address
[[Page 32483]]
methodologic and regulatory issues related to the co-development of two
or more investigational drugs intended to be used in combination.
II. Issues on Which FDA is Seeking Comment
All material submitted to this docket will be publicly available.
To facilitate development of guidance that meaningfully addresses the
concerns of those who may co-develop drugs intended to be used in
combination, FDA is seeking input on the following issues, and any
other issues relevant to developing FDA guidance:
1. General methodologic and regulatory issues that arise in the co-
development of two or more drugs intended to be used in combination
where the drugs are directed at providing a therapeutic effect on the
same symptom or manifestation of the disease or condition of interest,
including relevance and utility of clinical or animal findings for
either drug alone;
2. General methodologic and regulatory issues that arise in the co-
development of two or more drugs intended to be used in combination
where the drugs are directed at providing a therapeutic effect for the
same disease or condition, but act on different symptoms or
manifestations of that disease or condition, including relevance and
utility of clinical or animal findings for either drug alone;
3. General methodologic and regulatory issues that arise in the co-
development of two or more drugs intended to be used in combination
where one or more of the drugs is intended to enhance the effectiveness
of the other, but one or more of the drugs does not or may not have an
independent therapeutic effect, including relevance and utility of
clinical or animal findings for either drug alone; and
4. Methodologic and regulatory issues that arise in the co-
development of two or more drugs intended to be used in combination for
specific therapeutic categories, including oncology, anti-infectives,
seizure disorders, cardiovascular diseases, and any other therapeutic
category in which such co-development is likely to occur.
III. Submission of Comments
Interested parties may submit to the Division of Dockets Management
(see ADDRESSES) either electronic or written comments regarding this
document. It is only necesary to send one set of comments. It is no
longer necessary to send two copies of mailed comments. Identify
comments with the docket number found in brackets in the heading of
this document. Received comments may be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m., Monday through Friday.
Dated: June 2, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-13769 Filed 6-7-10; 8:45 am]
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