Human Gene Therapy for Rare Diseases; Guidance for Industry; Availability, 5451-5452 [2020-01704]
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Federal Register / Vol. 85, No. 20 / Thursday, January 30, 2020 / Notices
an understanding of the broad spectrum
of patients in a particular disease area.
Almost all non-Federal members of this
Committee serve as Special Government
Employees, with the exception of the
representatives from Industry.
III. Nomination Procedures
Any interested person may nominate
one or more qualified individuals for
membership on the Committee. Selfnominations are also accepted.
Nominations must include a cover
letter; a current, complete resume or
curriculum vitae for each nominee,
including current business and/or home
address, telephone number, and email
address, if available; and a signed copy
of the Acknowledgement and Consent
form available at the FDA Advisory
Nomination Portal (see ADDRESSES).
Nominations must specify the advisory
committee for which the nominee is
recommended.
Nominations must also acknowledge
that the nominee is aware of the
nomination unless self-nominated. FDA
will ask potential candidates to provide
detailed information concerning such
matters related to financial holdings,
employment, and research grants and/or
contracts to permit evaluation of
possible sources of conflicts of interest.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Dated: January 24, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–01659 Filed 1–29–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–D–2258]
Human Gene Therapy for Rare
Diseases; Guidance for Industry;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
khammond on DSKJM1Z7X2PROD with NOTICES
VerDate Sep<11>2014
16:56 Jan 29, 2020
Jkt 250001
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
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
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a final
guidance entitled ‘‘Human Gene
Therapy for Rare Diseases; Guidance for
Industry.’’ The final guidance document
provides recommendations to
stakeholders developing a human gene
therapy (GT) product intended to treat
a rare disease in adult and/or pediatric
patients regarding the manufacturing,
SUMMARY:
preclinical, and clinical trial design
issues for all phases of the clinical
development program. Such
information is intended to assist
sponsors in designing clinical
development programs for such
products, where there may be limited
study population size and potential
feasibility and safety issues as well as
issues relating to the interpretability of
bioactivity/efficacy outcomes that may
be unique to rare diseases or to the
nature of the GT product itself. The
guidance announced in this notice
finalizes the draft guidance of the same
title dated July 2018.
DATES: The announcement of the
guidance is published in the Federal
Register on January 30, 2020.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
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
PO 00000
Frm 00085
Fmt 4703
Sfmt 4703
5451
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2018–D–2258 for ‘‘Human Gene
Therapy for Rare Diseases; Guidance for
Industry.’’ 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.
• 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-201509-18/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.
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 Office of
Communication, Outreach and
Development, Center for Biologics
E:\FR\FM\30JAN1.SGM
30JAN1
5452
Federal Register / Vol. 85, No. 20 / Thursday, January 30, 2020 / Notices
khammond on DSKJM1Z7X2PROD with NOTICES
Evaluation and Research (CBER), Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 3128,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist the office in processing your
requests. The guidance may also be
obtained by mail by calling CBER at 1–
800–835–4709 or 240–402–8010. See
the SUPPLEMENTARY INFORMATION section
for electronic access to the guidance
document.
FOR FURTHER INFORMATION CONTACT:
Shruti Modi, Center for Biologics
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 7301,
Silver Spring, MD 20993–0002, 240–
402–7911.
SUPPLEMENTARY INFORMATION:
I. Background
The Orphan Drug Act of 1983 (Pub. L.
97–414) defines a rare disease as a
disease or condition that affects fewer
than 200,000 persons in the United
States. Since most rare diseases have no
approved therapies, there is a significant
unmet need for effective treatments.
However, developing safe and effective
products to treat rare diseases can be
challenging. For example, it may be
more difficult to find and recruit such
patients into clinical trials, and many
rare diseases exhibit a number of
variations or subtypes. Consequently,
patients may have highly diverse
clinical manifestations and rates of
disease progression with unpredictable
clinical courses. Despite these
challenges, GT-related research and
development continue to grow at a rapid
rate, with several products advancing in
clinical development.
FDA is announcing the availability of
a document entitled ‘‘Human Gene
Therapy for Rare Diseases; Guidance for
Industry.’’ This guidance provides
recommendations to stakeholders
developing human GT product intended
to treat a rare disease in adult and/or
pediatric patients regarding the
manufacturing, preclinical, and clinical
trial design issues for all phases of the
clinical development program. Such
information is intended to assist
sponsors in designing clinical
development programs for such
products, where there may be limited
study population size and potential
feasibility and safety issues as well as
issues relating to the interpretability of
bioactivity/efficacy outcomes that may
be unique to rare diseases or to the
nature of the GT product itself.
In the Federal Register of July 12,
2018 (83 FR 32303), FDA announced the
availability of the draft guidance of the
VerDate Sep<11>2014
16:56 Jan 29, 2020
Jkt 250001
same title. FDA received several
comments on the draft guidance and
those comments were considered as the
guidance was finalized. The guidance
announced in this notice finalizes the
draft guidance dated July 2018.
Elsewhere in this issue of the Federal
Register, FDA is announcing the
availability of two other human gene
therapy guidance documents entitled
‘‘Human Gene Therapy for Hemophilia;
Guidance for Industry’’ and ‘‘Human
Gene Therapy for Retinal Disorders;
Guidance for Industry.’’
This guidance is being issued
consistent with FDA’s good guidance
practices regulation (21 CFR 10.115).
The guidance represents the current
thinking of FDA on recommendations
for stakeholders developing human GT
products for retinal disorders affecting
adult and pediatric patients. 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
This guidance refers to previously
approved collections of information
subject to review by the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995
(44 U.S.C. 3501–3521). The collections
of information in 21 CFR part 50 have
been approved under OMB control
number 0910–0755; the collections of
information in 21 CFR part 58 have been
approved under OMB control number
0910–0119; the collections of
information in 21 CFR part 312 have
been approved under OMB control
number 0910–0014; the collections of
information in 21 CFR part 601 have
been approved under OMB control
number 0910–0338; the collections of
information in the guidance entitled
‘‘Expedited Programs for Serious
Conditions—Drugs and Biologics’’ have
been approved under OMB control
number 0910–0765; and the collections
of information in the guidance entitled
‘‘Formal Meetings Between the FDA and
Sponsors or Applicants’’ have been
approved under OMB control number
0910–0429.
III. Electronic Access
Persons with access to the internet
may obtain the guidance at either
https://www.fda.gov/vaccines-bloodbiologics/guidance-complianceregulatory-information-biologics/
biologics-guidances or https://
www.regulations.gov.
PO 00000
Frm 00086
Fmt 4703
Sfmt 4703
Dated: January 27, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–01704 Filed 1–29–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–D–2173]
Long Term Follow-Up After
Administration of Human Gene
Therapy Products; Guidance for
Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a final
guidance entitled ‘‘Long Term FollowUp After Administration of Human
Gene Therapy Products.’’ The guidance
document provides sponsors, who are
developing a human gene therapy (GT)
product, recommendations regarding
the design of long term follow-up
(LTFU) observational studies for the
collection of data on delayed adverse
events following administration of a GT
product. This guidance finalizes the
draft guidance of the same title dated
July 2018 and supersedes the document
entitled ‘‘Guidance for Industry: Gene
Therapy Clinical Trials—Observing
Subjects for Delayed Adverse Events’’
dated November 2006. This guidance
also supplements the guidance entitled
‘‘Testing of Retroviral Vector-Based
Human Gene Therapy Products for
Replication Competent Retrovirus
during Product Manufacture and Patient
Follow-up; Guidance for Industry.’’
DATES: The announcement of the
guidance is published in the Federal
Register on January 30, 2020.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
SUMMARY:
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
E:\FR\FM\30JAN1.SGM
30JAN1
Agencies
[Federal Register Volume 85, Number 20 (Thursday, January 30, 2020)]
[Notices]
[Pages 5451-5452]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01704]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2018-D-2258]
Human Gene Therapy for Rare Diseases; Guidance for Industry;
Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice of availability.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is announcing
the availability of a final guidance entitled ``Human Gene Therapy for
Rare Diseases; Guidance for Industry.'' The final guidance document
provides recommendations to stakeholders developing a human gene
therapy (GT) product intended to treat a rare disease in adult and/or
pediatric patients regarding the manufacturing, preclinical, and
clinical trial design issues for all phases of the clinical development
program. Such information is intended to assist sponsors in designing
clinical development programs for such products, where there may be
limited study population size and potential feasibility and safety
issues as well as issues relating to the interpretability of
bioactivity/efficacy outcomes that may be unique to rare diseases or to
the nature of the GT product itself. The guidance announced in this
notice finalizes the draft guidance of the same title dated July 2018.
DATES: The announcement of the guidance is published in the Federal
Register on January 30, 2020.
ADDRESSES: You may submit either electronic or written comments on
Agency guidances 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 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-2018-D-2258 for ``Human Gene Therapy for Rare Diseases; Guidance
for Industry.'' 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.
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.
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
Office of Communication, Outreach and Development, Center for Biologics
[[Page 5452]]
Evaluation and Research (CBER), Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 3128, Silver Spring, MD 20993-0002. Send
one self-addressed adhesive label to assist the office in processing
your requests. The guidance may also be obtained by mail by calling
CBER at 1-800-835-4709 or 240-402-8010. See the SUPPLEMENTARY
INFORMATION section for electronic access to the guidance document.
FOR FURTHER INFORMATION CONTACT: Shruti Modi, Center for Biologics
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 7301, Silver Spring, MD 20993-0002, 240-
402-7911.
SUPPLEMENTARY INFORMATION:
I. Background
The Orphan Drug Act of 1983 (Pub. L. 97-414) defines a rare disease
as a disease or condition that affects fewer than 200,000 persons in
the United States. Since most rare diseases have no approved therapies,
there is a significant unmet need for effective treatments. However,
developing safe and effective products to treat rare diseases can be
challenging. For example, it may be more difficult to find and recruit
such patients into clinical trials, and many rare diseases exhibit a
number of variations or subtypes. Consequently, patients may have
highly diverse clinical manifestations and rates of disease progression
with unpredictable clinical courses. Despite these challenges, GT-
related research and development continue to grow at a rapid rate, with
several products advancing in clinical development.
FDA is announcing the availability of a document entitled ``Human
Gene Therapy for Rare Diseases; Guidance for Industry.'' This guidance
provides recommendations to stakeholders developing human GT product
intended to treat a rare disease in adult and/or pediatric patients
regarding the manufacturing, preclinical, and clinical trial design
issues for all phases of the clinical development program. Such
information is intended to assist sponsors in designing clinical
development programs for such products, where there may be limited
study population size and potential feasibility and safety issues as
well as issues relating to the interpretability of bioactivity/efficacy
outcomes that may be unique to rare diseases or to the nature of the GT
product itself.
In the Federal Register of July 12, 2018 (83 FR 32303), FDA
announced the availability of the draft guidance of the same title. FDA
received several comments on the draft guidance and those comments were
considered as the guidance was finalized. The guidance announced in
this notice finalizes the draft guidance dated July 2018.
Elsewhere in this issue of the Federal Register, FDA is announcing
the availability of two other human gene therapy guidance documents
entitled ``Human Gene Therapy for Hemophilia; Guidance for Industry''
and ``Human Gene Therapy for Retinal Disorders; Guidance for
Industry.''
This guidance is being issued consistent with FDA's good guidance
practices regulation (21 CFR 10.115). The guidance represents the
current thinking of FDA on recommendations for stakeholders developing
human GT products for retinal disorders affecting adult and pediatric
patients. 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
This guidance refers to previously approved collections of
information subject to review by the Office of Management and Budget
(OMB) under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3521).
The collections of information in 21 CFR part 50 have been approved
under OMB control number 0910-0755; the collections of information in
21 CFR part 58 have been approved under OMB control number 0910-0119;
the collections of information in 21 CFR part 312 have been approved
under OMB control number 0910-0014; the collections of information in
21 CFR part 601 have been approved under OMB control number 0910-0338;
the collections of information in the guidance entitled ``Expedited
Programs for Serious Conditions--Drugs and Biologics'' have been
approved under OMB control number 0910-0765; and the collections of
information in the guidance entitled ``Formal Meetings Between the FDA
and Sponsors or Applicants'' have been approved under OMB control
number 0910-0429.
III. Electronic Access
Persons with access to the internet may obtain the guidance at
either https://www.fda.gov/vaccines-blood-biologics/guidance-compliance-regulatory-information-biologics/biologics-guidances or
https://www.regulations.gov.
Dated: January 27, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-01704 Filed 1-29-20; 8:45 am]
BILLING CODE 4164-01-P