[Federal Register Volume 67, Number 2 (Thursday, January 3, 2002)]
[Notices]
[Page 342]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 02-12]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of Co-Exclusive License: ``cDNA for Human and
Pig Dihydropyrimidine Dehydrogenase'
AGENCY: National Institutes of Health, Public Health Service, DHHS.
ACTION: Notice.
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SUMMARY: This is notice, in accordance with 35 U.S.C. 209(c)(1) and 37
CFR 404.7(a)(1)(i), that the National Institutes of Health, Department
of Health and Human Services, is contemplating the grant of an co-
exclusive license to practice the inventions embodied in U.S. Patents
5,856,454 and 6,015,673, entitled ``cDNA for Human and Pig
Dihydropyrimidine Dehydrogenase'' to Variagenics, Inc. of Cambridge,
MA.
The prospective co-exclusive license territory will be worldwide
and the field of use may be limited to in vitro diagnostics.
DATES: Only written comments and/or license applications which are
received by the National Institutes of Health on or before March 4,
2002 will be considered.
ADDRESSES: Requests for copies of the patents, inquiries, comments, and
other materials relating to the contemplated co-exclusive license
should be directed to: Matthew B. Kiser, Technology Licensing
Specialist, Office of Technology Transfer, National Institutes of
Health, 6011 Executive Boulevard, Suite 325, Rockville, MD 20852-3804;
Telephone: (301) 496-7056 x224; Facsimile (301) 402-0220; E-mail
[email protected].
SUPPLEMENTARY INFORMATION: The technology relates to the DPD gene.
Cancer patients having a DPD deficiency are at risk of a severe toxic
reaction to the commonly used anticancer agent 5-fluorouracil (5-FU).
Claimed are DPD genes from human and pig, methods for detecting the
level of nucleic acids that encode DPD in patient, and nucleic acids
that are useful as probes for this purpose.
The prospective co-exclusive license will be royalty-bearing and
will comply with the terms and conditions of 35 U.S.C. 209 and 37 CFR
404.7. The prospective co-exclusive license may be granted unless
within sixty (60) days from the date of this published notice, the NIH
receives written evidence and argument that establish that the grant of
the license would not be consistent with the requirements of 35 U.S.C.
209 and 37 CFR 404.7.
Applications for a license in the field of use filed in response to
this notice will be treated as objections to the grant of the
contemplated co-exclusive license. Comments and objections submitted to
this notice will not be made available for public inspection and, to
the extent permitted by law, will not be released under the Freedom of
Information Act, 5 U.S.C. 552.
Dated: December 20, 2001.
Jack Spiegel,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer.
[FR Doc. 02-12 Filed 1-2-02; 8:45 am]
BILLING CODE 4140-01-P