[Federal Register Volume 62, Number 54 (Thursday, March 20, 1997)]
[Notices]
[Pages 13388-13389]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-6977]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 96E-0440]
Determination of Regulatory Review Period for Purposes of Patent
Extension; HYCAMTINTM
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) has determined the
regulatory review period for HYCAMTINTM and is publishing this
notice of that determination as required by law. FDA has made the
determination because of the submission of an application to the
Commissioner of Patents and Trademarks, Department of Commerce, for the
extension of a patent which claims that human drug product.
ADDRESSES: Written comments and petitions should be directed to the
Dockets Management Branch (HFA-305), Food and Drug Administration,
12420 Parklawn Dr., rm. 1-23, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: Brian J. Malkin, Office of Health
Affairs (HFY-20), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-443-1382.
SUPPLEMENTARY INFORMATION: The Drug Price Competition and Patent Term
Restoration Act of 1984 (Pub. L. 98-417) and the Generic Animal Drug
and Patent Term Restoration Act (Pub. L. 100-670) generally provide
that a patent may be extended for a period of up to 5 years so long as
the patented item (human drug product, animal drug product, medical
device, food additive, or color additive) was subject to regulatory
review by FDA before the item was marketed. Under these acts, a
product's regulatory review period forms the basis for determining the
amount of extension an applicant may receive.
A regulatory review period consists of two periods of time: A
testing phase and an approval phase. For human drug products, the
testing phase begins when the exemption to permit the clinical
investigations of the drug becomes effective and runs until the
approval phase begins. The approval phase starts with the initial
submission of an application to market the human drug product and
continues until FDA grants permission to market the drug product.
Although only a portion of a regulatory review period may count toward
the actual amount of extension that the Commissioner of Patents and
Trademarks may award (for example, half the testing phase must be
subtracted as well as any time that may have occurred before the patent
was issued), FDA's determination of the length of a regulatory review
period for a human drug product will include all of the testing phase
and approval phase as specified in 35 U.S.C. 156(g)(1)(B).
FDA recently approved for marketing the human drug product
HYCAMTINTM (topotecan hydrochloride). HYCAMTINTM is indicated
for the treatment of patients with metastatic carcinoma of the ovary
after failure of initial or subsequent chemotherapy. Subsequent to this
approval, the Patent and Trademark Office received a patent term
restoration application for HYCAMTINTM (U.S. Patent No. 5,004,758)
from SmithKline Beecham Corp. and the Patent and Trademark Office
requested FDA's assistance in determining this patent's eligibility for
patent term restoration. In a letter dated January 13, 1997, FDA
advised the Patent and Trademark Office that this human drug product
had undergone a regulatory review period and that the approval of
HYCAMTINTM represented the first permitted commercial marketing or
use of the product. Shortly thereafter, the Patent and Trademark Office
requested that FDA determine the product's regulatory review period.
FDA has determined that the applicable regulatory review period for
HYCAMTINTM is 2,644 days. Of this time, 2,485 days occurred during
the testing phase of the regulatory review period, while 159 days
occurred during the approval phase. These periods of time were derived
from the following dates:
1. The date an exemption under section 505(i) of the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 355(i)) became effective: March 4,
1989. The applicant claims January 30, 1989, as the date the
investigational new drug application (IND) for HYCAMTINTM (IND
32,693) became effective. However, FDA records indicate that IND 32,693
was received at FDA on February 2, 1989, and became effective 30 days
later on March 4, 1989.
2. The date the application was initially submitted with respect to
the human drug product under section
[[Page 13389]]
505(b) of the Federal Food, Drug, and Cosmetic Act: December 22, 1995.
The applicant claims December 21, 1995, as the date the new drug
application (NDA) for HYCAMTINTM (NDA 20-671) was initially
submitted. However, FDA records indicate that NDA 20-671 was submitted
on December 22, 1995.
3. The date the application was approved: May 28, 1996. FDA has
verified the applicant's claim that NDA 20-671 was approved on May 28,
1996.
This determination of the regulatory review period establishes the
maximum potential length of a patent extension. However, the U.S.
Patent and Trademark Office applies several statutory limitations in
its calculations of the actual period for patent extension. In its
application for patent extension, this applicant seeks 572 days of
patent term extension.
Anyone with knowledge that any of the dates as published is
incorrect may, on or before May 20, 1997, submit to the Dockets
Management Branch (address above) written comments and ask for a
redetermination. Furthermore, any interested person may petition FDA,
on or before September 22, 1997, for a determination regarding whether
the applicant for extension acted with due diligence during the
regulatory review period. To meet its burden, the petition must contain
sufficient facts to merit an FDA investigation. (See H. Rept. 857, part
1, 98th Cong., 2d sess., pp. 41-42, 1984.) Petitions should be in the
format specified in 21 CFR 10.30.
Comments and petitions should be submitted to the Dockets
Management Branch (address above) in three copies (except that
individuals may submit single copies) and identified with the docket
number found in brackets in the heading of this document. Comments and
petitions may be seen in the Dockets Management Branch between 9 a.m.
and 4 p.m., Monday through Friday.
Dated: March 12, 1997.
Stuart L. Nightingale,
Associate Commissioner for Health Affairs.
[FR Doc. 97-6977 Filed 3-19-97; 8:45 am]
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