65FR37396 Draft Guidance for Industry on Development of Parathyroid Hormone for the Prevention and Treatment of Osteoporosis; Availability
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Posting-number: Volume 65, Issue 115, Page 37396
[Federal Register: June 14, 2000 (Volume 65, Number 115)]
[Notices]
[Page 37396]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr14jn00-85]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 00D-1307]
Draft Guidance for Industry on Development of Parathyroid Hormone
for the Prevention and Treatment of Osteoporosis; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing the
availability of a draft guidance for industry entitled ``Development of
Parathyroid Hormone for the Prevention and Treatment of Osteoporosis.''
Parathyroid hormone (PTH) is being studied for use in the prevention
and treatment of osteoporosis. In response to preclinical studies
submitted to FDA in which osteosarcomas developed in rats and mice
following administration of PTH and related peptides, the agency is
developing guidance for the development of PTH as a drug for
osteoporosis. This guidance is intended to improve the benefit to risk
ratio of treatment with PTH and related peptides.
DATES: Submit written comments on the draft guidance by August 14,
2000. General comments on agency guidance documents are welcome at any
time.
ADDRESSES: Copies of this draft guidance for industry are available on
the Internet at http://www.fda.gov/cder/guidance/index.htm. Submit
written requests for single copies of the draft guidance to the Drug
Information Branch (HFD-210), Center for Drug Evaluation and Research,
Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857.
Send one self-addressed adhesive label to assist that office in
processing your requests. Submit written comments on the draft guidance
to the Dockets Management Branch (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Eric Colman, Center for Drug
Evaluation and Research (HFD-510), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-827-6371.
SUPPLEMENTARY INFORMATION: FDA is announcing the availability of a
draft guidance for industry entitled ``Development of Parathyroid
Hormone for the Prevention and Treatment of Osteoporosis.'' This draft
guidance is being issued in response to information submitted to the
agency regarding the development of osteosarcomas in two strains of
rats and one strain of mice following treatment with PTH and related
peptides from weaning to 18 months. Given the uncertain clinical
relevance of the findings in rodents, and in an effort to improve the
benefit to risk ratio of PTH when used in studies of the prevention
and/or treatment of osteoporosis, the draft guidance recommends that
special consideration be given to the design and conduct of clinical
trials evaluating the safety and effectiveness of PTH. These special
considerations relate to inclusion and exclusion criteria, patient
followup, and patient informed consent.
This draft guidance is being issued consistent with FDA's good
guidance practices (62 FR 8961, February 27, 1997). The draft guidance
represents the agency's current thinking on the development of
parathyroid hormone in the prevention and treatment of osteoporosis. It
does not create or confer any rights for or on any person and does not
operate to bind FDA or the public. An alternative approach may be used
if such approach satisfies the requirements of the applicable statutes,
regulations, or both.
Interested persons may submit to the Dockets Management Branch
(address above) written comments on the draft guidance. Two copies of
any comments are to be submitted, except that individuals may submit
one copy. Comments are to be identified with the docket number found in
brackets in the heading of this document. The draft guidance and
received comments are available for public examination in the Dockets
Management Branch between 9 a.m. and 4 p.m., Monday through Friday.
Dated: June 6, 2000.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 00-14986 Filed 6-13-00; 8:45 am]
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