Grant of Interim Extension of the Term of U.S. Patent No. 4,971,802; MIFAMURTIDE, 58649 [E7-20372]
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Federal Register / Vol. 72, No. 199 / Tuesday, October 16, 2007 / Notices
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[FR Doc. E7–20322 Filed 10–15–07; 8:45 am]
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DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No. PTO–P–2007–0037]
Authority: 16 U.S.C. 1801 et seq.
Dated: October 11, 2007.
Alan D. Risenhoover,
Director, Office of Sustainable Fisheries,
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[FR Doc. 07–5107 Filed 10–11–07; 4:13 pm]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
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North Pacific Fishery Management
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National Marine Fisheries
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ACTION:
Notice of a public meeting.
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The meeting will be held at
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Council address: North Pacific
Fishery Management Council, 605 W.
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04:12 Oct 16, 2007
Jkt 214001
United States Patent and
Trademark Office, Commerce.
ACTION: Notice of Interim Patent Term
Extension.
AGENCY:
SUMMARY: The United States Patent and
Trademark Office has issued a
certificate under 35 U.S.C. 156(d)(5) for
a one-year interim extension of the term
of U.S. Patent No. 4,971,802.
FOR FURTHER INFORMATION CONTACT: Raul
Tamayo by telephone at (571) 272–7728;
by mail marked to his attention and
addressed to the Commissioner for
Patents, Mail Stop Hatch-Waxman PTE,
P.O. Box 1450, Alexandria, VA 22313–
1450; by fax marked to his attention at
(571) 273–7728, or by e-mail to
Raul.Tamayo@uspto.gov.
Section
156 of Title 35, United States Code,
generally provides that the term of a
patent may be extended for a period of
up to five years if the patent claims a
product, or a method of making or using
a product, that has been subject to
certain defined regulatory review, and
that the patent may be extended for
interim periods of up to a year if the
regulatory review is anticipated to
extend beyond the expiration date of the
patent.
On August 8, 2007, IDM Pharma,
agent/licensee of patent owner Novartis,
timely filed an application under 35
U.S.C. 156(d)(5) for an interim extension
of the term of U.S. Patent No. 4,971,802.
Claims of the patent cover the product
Mifamurtide having the active
ingredient muramyl tripeptide
phosphatidyl ethanolamine. The
application indicates, and the Food and
Drug Administration has confirmed,
that a New Drug Application for the
human drug product Mifamurtide has
been filed and is currently undergoing
regulatory review before the Food and
Drug Administration for permission to
market or use the product commercially.
Review of the application indicates
that, except for permission to market or
SUPPLEMENTARY INFORMATION:
SUMMARY: The North Pacific Fishery
Management Council (Council) Salmon
Bycatch Workgroup will meet in
Anchorage, AK.
VerDate Aug<31>2005
Grant of Interim Extension of the Term
of U.S. Patent No. 4,971,802;
MIFAMURTIDE
PO 00000
Frm 00019
Fmt 4703
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58649
use the product commercially, the
subject patent would be eligible for an
extension of the patent term under 35
U.S.C. 156, and that the patent should
be extended for one year as required by
35 U.S.C. 156(d)(5)(B). Because it is
apparent that the regulatory review
period will continue beyond the
expiration date of the patent (November
20, 2007), interim extension of the
patent term under 35 U.S.C. 156(d)(5) is
appropriate.
An interim extension under 35 U.S.C.
156(d)(5) of the term of U.S. Patent No.
4,971,802 is granted for a period of one
year from the expiration date of the
patent, i.e., until November 20, 2008.
Dated: October 4, 2007.
Jon W. Dudas,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. E7–20372 Filed 10–15–07; 8:45 am]
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DEPARTMENT OF ENERGY
Federal Energy Regulatory
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[IC07–574–001, FERC–574]
Commission Information Collection
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Comment Request; Extension
October 4, 2007.
Federal Energy Regulatory
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ACTION: Notice.
AGENCY:
SUMMARY: In compliance with the
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Paperwork Reduction Act of 1995, 44
U.S.C. 3507, the Federal Energy
Regulatory Commission (Commission)
has submitted the information
collection described below to the Office
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Federal Register notice of May 29, 2007
(72 FR 29489–29490) and has made this
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2007.
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E:\FR\FM\16OCN1.SGM
16OCN1
Agencies
[Federal Register Volume 72, Number 199 (Tuesday, October 16, 2007)]
[Notices]
[Page 58649]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-20372]
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DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No. PTO-P-2007-0037]
Grant of Interim Extension of the Term of U.S. Patent No.
4,971,802; MIFAMURTIDE
AGENCY: United States Patent and Trademark Office, Commerce.
ACTION: Notice of Interim Patent Term Extension.
-----------------------------------------------------------------------
SUMMARY: The United States Patent and Trademark Office has issued a
certificate under 35 U.S.C. 156(d)(5) for a one-year interim extension
of the term of U.S. Patent No. 4,971,802.
FOR FURTHER INFORMATION CONTACT: Raul Tamayo by telephone at (571) 272-
7728; by mail marked to his attention and addressed to the Commissioner
for Patents, Mail Stop Hatch-Waxman PTE, P.O. Box 1450, Alexandria, VA
22313-1450; by fax marked to his attention at (571) 273-7728, or by e-
mail to Raul.Tamayo@uspto.gov.
SUPPLEMENTARY INFORMATION: Section 156 of Title 35, United States Code,
generally provides that the term of a patent may be extended for a
period of up to five years if the patent claims a product, or a method
of making or using a product, that has been subject to certain defined
regulatory review, and that the patent may be extended for interim
periods of up to a year if the regulatory review is anticipated to
extend beyond the expiration date of the patent.
On August 8, 2007, IDM Pharma, agent/licensee of patent owner
Novartis, timely filed an application under 35 U.S.C. 156(d)(5) for an
interim extension of the term of U.S. Patent No. 4,971,802. Claims of
the patent cover the product Mifamurtide having the active ingredient
muramyl tripeptide phosphatidyl ethanolamine. The application
indicates, and the Food and Drug Administration has confirmed, that a
New Drug Application for the human drug product Mifamurtide has been
filed and is currently undergoing regulatory review before the Food and
Drug Administration for permission to market or use the product
commercially.
Review of the application indicates that, except for permission to
market or use the product commercially, the subject patent would be
eligible for an extension of the patent term under 35 U.S.C. 156, and
that the patent should be extended for one year as required by 35
U.S.C. 156(d)(5)(B). Because it is apparent that the regulatory review
period will continue beyond the expiration date of the patent (November
20, 2007), interim extension of the patent term under 35 U.S.C.
156(d)(5) is appropriate.
An interim extension under 35 U.S.C. 156(d)(5) of the term of U.S.
Patent No. 4,971,802 is granted for a period of one year from the
expiration date of the patent, i.e., until November 20, 2008.
Dated: October 4, 2007.
Jon W. Dudas,
Under Secretary of Commerce for Intellectual Property and Director of
the United States Patent and Trademark Office.
[FR Doc. E7-20372 Filed 10-15-07; 8:45 am]
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