[Federal Register Volume 59, Number 48 (Friday, March 11, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-5635]


[[Page Unknown]]

[Federal Register: March 11, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 92E-0472]

 

Determination of Regulatory Review Period for Purposes of Patent 
Extension; Sporanox

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 Sporanox 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, rm. 
1-23, 12420 Parklawn Dr., 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 
Sporanox. Sporanox (itraconazole) is indicated for 
the treatment of the following fungal infections in immunocompromised 
and nonimmunocompromised patients: (1) blastomycosis, pulmonary and 
extrapulmonary, and (2) histoplasmosis, including chronic cavitary 
pulmonary disease and disseminated, nonmeningeal histoplasmosis. 
Subsequent to this approval, the Patent and Trademark Office received a 
patent term restoration application for Sporanox (U.S. Patent 
No. 4,267,179) from Janssen Pharmaceutica N.V., and the Patent and 
Trademark Office requested FDA's assistance in determining this 
patents's eligibility for patent term restoration. FDA, in a letter 
dated December 8, 1992, advised the Patent and Trademark Office that 
this human drug product had undergone a regulatory review period and 
that the approval of Sporanox represented the first 
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 
Sporanox is 2,990 days. Of this time, 2,155 days occurred 
during the testing phase of the regulatory review period, while 835 
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 became effective: July 7, 1984. The applicant 
claims June 7, 1984, as the date the investigational new drug 
application (IND) became effective. However, FDA records indicate that 
the IND effective date was July 7, 1984, which was 30 days after FDA 
receipt of the IND.
    2. The date the application was initially submitted with respect to 
the human drug product under section 505(b) of the Federal Food, Drug, 
and Cosmetic Act: May 31, 1990. The applicant claims May 30, 1990, as 
the date the new drug application (NDA) for Sporanox (NDA 20-
083) was initially submitted. However, FDA records indicate that NDA 
20-083 was initially submitted on May 31, 1990.
    3. The date the application was approved: September 11, 1992. FDA 
has verified the applicant's claim that NDA 20-083 was approved on 
September 11, 1992.
    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 1,510 days of 
patent term extension.
    Anyone with knowledge that any of the dates as published is 
incorrect may, on or before May 10, 1994, 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 7, 1994, 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: December 28, 1993.
Stuart L. Nightingale,
Associate Commissioner for Health Affairs.
[FR Doc. 94-5635 Filed 3-10-94; 8:45 am]
BILLING CODE 4160-01-F