[Federal Register Volume 85, Number 136 (Wednesday, July 15, 2020)]
[Notices]
[Pages 42880-42882]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-15243]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2020-D-1400]
Use of Real-World Data and Real-World Evidence To Support
Effectiveness of New Animal Drugs; Draft Guidance for Industry;
Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice of availability.
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SUMMARY: The Food and Drug Administration (FDA or Agency) is announcing
the availability of a draft guidance for industry (GFI) #266 entitled
``Use of Real-World Data and Real-World Evidence to Support
Effectiveness of New Animal Drugs.'' The draft guidance, if finalized,
will describe FDA's current thinking with respect to assisting sponsors
in incorporating real-world data and real-world evidence (including
ongoing surveillance activities, observational studies, and registry
data) into proposed clinical investigation protocols and applications
for new animal drugs under the Federal Food, Drug, and Cosmetic Act
(FD&C Act).
DATES: Submit either electronic or written comments on the draft
guidance by October 13, 2020 to ensure that the Agency considers your
comment on this draft guidance before it begins work on the final
version of the guidance.
ADDRESSES: You may submit comments on any guidance at any time as
follows:
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to https://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or
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confidential business information, such as a manufacturing process.
Please note that if you include your name, contact information, or
other information that identifies you in the body of your comments,
that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2020-D-1400 for ``Use of Real-World Data and Real-World Evidence to
Support Effectiveness of New Animal Drugs.'' Received comments will be
placed in the docket and, except for those submitted as ``Confidential
Submissions,'' publicly viewable at https://www.regulations.gov or at
the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through
Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will
review this copy, including the claimed confidential information, in
its consideration of comments. The second copy, which will have the
claimed confidential information redacted/blacked out, will be
available for public viewing and posted on https://www.regulations.gov.
Submit both copies to the Dockets Management Staff. If you do not wish
your name and contact information to be made publicly available, you
can provide this information on the cover sheet and not in the body of
your comments and you must identify this information as
``confidential.'' Any information marked as ``confidential'' will not
be disclosed except in accordance with 21 CFR 10.20 and other
applicable disclosure law. For more information about FDA's posting of
comments to public dockets, see 80 FR 56469, September 18, 2015, or
access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
You may submit comments on any guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single copies of the guidance to the
Policy and Regulations Staff (HFV-6), Center for Veterinary Medicine,
Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855.
Send one self-addressed adhesive label to assist that office in
processing your requests. See the SUPPLEMENTARY INFORMATION section for
electronic access to the draft guidance document.
FOR FURTHER INFORMATION CONTACT: Susan Storey, Center for Veterinary
Medicine (HFV-131), Food and Drug Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240-402-0578, [email protected].
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of draft GFI #266 entitled ``Use
of Real-World Data and Real-World Evidence to Support Effectiveness of
New Animal Drugs.'' Section 305 of the Animal Drug and Animal Generic
Drug User Fee Amendments of 2018 (Pub. L. 115-234), among other things,
directed FDA to hold a public meeting for interested parties to discuss
innovative animal drug investigation designs and to issue guidance
addressing the incorporation of the use of such elements of
investigations as complex adaptive and other novel investigation
designs, data from foreign countries, real-world evidence (including
ongoing surveillance activities, observational studies, and registry
data), biomarkers, and surrogate endpoints into proposed clinical
investigation protocols and applications for new animal drugs.
In the Federal Register of July 9, 2019 (84 FR 32749), FDA's Center
for Veterinary Medicine (CVM) published a notice of a public meeting
entitled ``Incorporating Alternative Approaches in Clinical
Investigations for New Animal Drugs'' giving interested persons until
August 17, 2019, to comment on the topics discussed at the public
meeting and the questions published in the meeting notice (84 FR 32749
at 32750 to 32751). On August 13, 2019, we published a notice
announcing the extension of the comment period to September 16, 2019
(84 FR 40071). CVM received numerous comments on the topics discussed
at the public meeting and the questions published in the meeting notice
and those comments were considered as the draft GFI #266 was developed.
This draft guidance describes how CVM intends to evaluate real-
world data and real-world evidence in submissions to CVM to demonstrate
substantial evidence of effectiveness for new animal drug applications
or a reasonable expectation of effectiveness for applications for
conditional approval of a new animal drug. It also provides information
about how sponsors may obtain feedback from CVM on technical issues
related to the use of real-world data and real-world evidence before
the submission of an application.
This level 1 draft guidance is being issued consistent with FDA's
good guidance practices regulation (21 CFR 10.115). The draft guidance,
if finalized, will represent the current thinking of FDA regarding the
use of real-world data and real-world evidence (including ongoing
surveillance activities, observational studies, and registry data) in
submissions to CVM to support the effectiveness of new animal drugs. It
does not establish any rights for any person and is not binding on FDA
or the public. You can use an alternative approach if it satisfies the
requirements of the applicable statutes and regulations.
II. Paperwork Reduction Act of 1995
FDA tentatively concludes that this draft guidance contains no
collection of information. Therefore, clearance by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3521) is not required.
However, this draft guidance refers to previously approved FDA
collections of information found in FDA regulations for new animal drug
applications submitted under section 512(b) (21 U.S.C. 360b(b)) and 571
(21 U.S.C. 360ccc-1) of the FD&C Act. These collections of information
are subject to review by OMB under the PRA. The collections of
information in 21 CFR
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part 514 have been approved under OMB control number 0910-0032.
III. Electronic Access
Persons with access to the internet may obtain the draft guidance
at either https://www.fda.gov/animal-veterinary/guidance-regulations/guidance-industry or https://www.regulations.gov.
Dated: July 9, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-15243 Filed 7-14-20; 8:45 am]
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