Prospective Grant of Exclusive License: Use of Licensee's proprietary delivery formulation containing synthetic peptides of the CEA antigen (or modifications, derivatives, fragments, or immunogenic epitopes thereof) as claimed in the Licensed Patent Rights, alone or in combination with at least one other synthetic peptide for use in the prevention and/or treatment of adenocarcinomas in humans. For the avoidance of doubt, said delivery formulation specifically excludes all poxviruses, eukaryotic expression vectors, and recombinant yeast, 26413 [E7-8888]
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Federal Register / Vol. 72, No. 89 / Wednesday, May 9, 2007 / Notices
Dated: May 2, 2007.
Judith Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 07–2299 Filed 5–8–07; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive
License: Use of Licensee’s proprietary
delivery formulation containing
synthetic peptides of the CEA antigen
(or modifications, derivatives,
fragments, or immunogenic epitopes
thereof) as claimed in the Licensed
Patent Rights, alone or in combination
with at least one other synthetic
peptide for use in the prevention and/
or treatment of adenocarcinomas in
humans. For the avoidance of doubt,
said delivery formulation specifically
excludes all poxviruses, eukaryotic
expression vectors, and recombinant
yeast
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
sroberts on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: This is notice, in accordance
with 35 U.S.C. 209(c)(1) and 37 CFR
Part 404.7(a)(1)(i), that the National
Institutes of Health, Department of
Health and Human Services, is
contemplating the grant of an exclusive
patent license to practice the inventions
embodied in U.S. Patent 6,756,038 and
PCT Application Serial No. PCT/US98/
19794 and foreign equivalents thereof,
entitled ‘‘Agonist and Antagonist
Peptides of Carcinoembryonic Antigen
(CEA)’’ (E–099–1996/0), to Immatics
Biotechnologies, GmbH, which is
located in Tuebingen, Germany. The
patent rights in these inventions have
been assigned to the United States of
America.
The prospective exclusive license
territory may be worldwide and the
field of use may be limited to the use
of Licensee’s proprietary delivery
formulation containing synthetic
peptides of the CEA antigen (or
modifications, derivatives, fragments, or
immunogenic epitopes thereof) as
claimed in the Licensed Patent Rights,
alone or in combination with at least
one other synthetic peptide for use in
the prevention and/or treatment of
adenocarcinomas in humans. For the
avoidance of doubt, said delivery
formulation specifically excludes all
poxviruses, eukaryotic expression
vectors, and recombinant yeast.
VerDate Aug<31>2005
18:12 May 08, 2007
Jkt 211001
Only written comments and/or
applications for a license which are
received by the NIH Office of
Technology Transfer on or before July 9,
2007 will be considered.
ADDRESSES: Requests for copies of the
patent application, inquiries, comments,
and other materials relating to the
contemplated exclusive license should
be directed to: Michelle A. Booden,
PhD., Technology Licensing Specialist,
Office of Technology Transfer, National
Institutes of Health, 6011 Executive
Boulevard, Suite 325, Rockville, MD
20852–3804; Telephone: (301) 451–
7337; Facsimile: (301) 402–0220; E-mail:
boodenm@mail.nih.gov.
SUPPLEMENTARY INFORMATION: The
technology describes the composition
and use of nucleic acid sequences that
encode agonist and one antagonist
peptide variants of the human
carcinoembryonic antigen (CEA)
peptide, including but not limited to
CAP–1. CEA is an antigen, which is
expressed on the surface of various
types of cancer cells. It is capable of
stimulating a specific cytolytic T cell
response, as is CAP–1, which is a highly
immunogenic epitope of CEA.
Therefore, CAP–1 agonists which are
capable of eliciting a CEA-specific
cytolytic T cell response, such as those
identified by the inventors, may
represent potential immunogens for use
as therapeutic agents or vaccines against
various cancers, and possibly also for
use against autoimmune diseases. In
fact, at least one of the agonist peptides
appears to be more immunogenic than
the native CAP–1 peptide. CAP–1
antagonists which are capable of
reducing or eliminating this T cell
response, such as the antagonist peptide
variant identified by the inventors, may
represent potential agents for use
against autoimmune responses to CEA
or to agonist peptide variants thereof.
The prospective exclusive license will
be royalty bearing and will comply with
the terms and conditions of 35 U.S.C.
209 and 37 CFR Part 404.7. The
prospective 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 establishes that the grant
of the license would not be consistent
with the requirements of 35 U.S.C. 209
and 37 CFR Part 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 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
DATES:
PO 00000
Frm 00081
Fmt 4703
Sfmt 4703
26413
under the Freedom of Information Act,
5 U.S.C. 552.
Dated: May 1, 2007.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E7–8888 Filed 5–8–07; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of an Exclusive
License: Development and
Commercialization of Therapeutic
Products for Rheumatoid Arthritis (RA)
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
AGENCY:
SUMMARY: This notice, in accordance
with 35 U.S.C. § 209(c)(1) and 37 CFR
Part 404.7(a)(1)(i), announces that the
Department of Health and Human
Services is contemplating the grant of an
exclusive license to practice the
inventions embodied in PCT
Application No. PCT/US01/04125, filed
February 9, 2001, entitled
‘‘Identification of a Novel Domain in the
Tumor Necrosis Factor Receptor Family
that Mediates Pre-ligand Receptor
Assembly and Function’’ [E–095–2000/
0–PCT–02]; U.S. Patent No. 7,148,061,
issued December 12, 2006, entitled
‘‘Identification of Novel Domain in the
Tumor Necrosis Factor Receptor Family
that Mediates Pre-ligand Receptor
Assembly and Function’’ [E–095–2000/
0–US–03]; U.S. Patent Application No.
11/637,272, filed December 12, 2006,
entitled ‘‘Identification of Novel Domain
in the Tumor Necrosis Factor Receptor
Family that Mediates Pre-ligand
Receptor Assembly and Function’’ [E–
095–2000/0–US–08]; PCT Application
No. PCT/US06/24909, filed June 26,
2006, entitled ‘‘A Potential Novel
Therapeutic Protein Molecule of
Inflammatory Arthritis Targeting the
Pre-ligand Assembly Domain (PLAD) of
Tumor Necrosis Factor Receptor Type
1’’ [E–095–2000/4–PCT–01]; European
Patent Application No. 01910476.9,
filed February 9, 2001, entitled
‘‘Identification of Novel Domain in the
Tumor Necrosis Factor Receptor Family
that Mediates Pre-ligand Receptor
Assembly and Function’’ [E–095–2000/
0–EP–06]; Australian Patent Application
No. 2001238076, filed on February 9,
2001, entitled ‘‘Identification of Novel
Domain in the Tumor Necrosis Factor
Receptor Family that Mediates Pre-
E:\FR\FM\09MYN1.SGM
09MYN1
Agencies
[Federal Register Volume 72, Number 89 (Wednesday, May 9, 2007)]
[Notices]
[Page 26413]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-8888]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive License: Use of Licensee's
proprietary delivery formulation containing synthetic peptides of the
CEA antigen (or modifications, derivatives, fragments, or immunogenic
epitopes thereof) as claimed in the Licensed Patent Rights, alone or in
combination with at least one other synthetic peptide for use in the
prevention and/or treatment of adenocarcinomas in humans. For the
avoidance of doubt, said delivery formulation specifically excludes all
poxviruses, eukaryotic expression vectors, and recombinant yeast
AGENCY: National Institutes of Health, Public Health Service, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This is notice, in accordance with 35 U.S.C. 209(c)(1) and 37
CFR Part 404.7(a)(1)(i), that the National Institutes of Health,
Department of Health and Human Services, is contemplating the grant of
an exclusive patent license to practice the inventions embodied in U.S.
Patent 6,756,038 and PCT Application Serial No. PCT/US98/19794 and
foreign equivalents thereof, entitled ``Agonist and Antagonist Peptides
of Carcinoembryonic Antigen (CEA)'' (E-099-1996/0), to Immatics
Biotechnologies, GmbH, which is located in Tuebingen, Germany. The
patent rights in these inventions have been assigned to the United
States of America.
The prospective exclusive license territory may be worldwide and
the field of use may be limited to the use of Licensee's proprietary
delivery formulation containing synthetic peptides of the CEA antigen
(or modifications, derivatives, fragments, or immunogenic epitopes
thereof) as claimed in the Licensed Patent Rights, alone or in
combination with at least one other synthetic peptide for use in the
prevention and/or treatment of adenocarcinomas in humans. For the
avoidance of doubt, said delivery formulation specifically excludes all
poxviruses, eukaryotic expression vectors, and recombinant yeast.
DATES: Only written comments and/or applications for a license which
are received by the NIH Office of Technology Transfer on or before July
9, 2007 will be considered.
ADDRESSES: Requests for copies of the patent application, inquiries,
comments, and other materials relating to the contemplated exclusive
license should be directed to: Michelle A. Booden, PhD., Technology
Licensing Specialist, Office of Technology Transfer, National
Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville,
MD 20852-3804; Telephone: (301) 451-7337; Facsimile: (301) 402-0220; E-
mail: boodenm@mail.nih.gov.
SUPPLEMENTARY INFORMATION: The technology describes the composition and
use of nucleic acid sequences that encode agonist and one antagonist
peptide variants of the human carcinoembryonic antigen (CEA) peptide,
including but not limited to CAP-1. CEA is an antigen, which is
expressed on the surface of various types of cancer cells. It is
capable of stimulating a specific cytolytic T cell response, as is CAP-
1, which is a highly immunogenic epitope of CEA. Therefore, CAP-1
agonists which are capable of eliciting a CEA-specific cytolytic T cell
response, such as those identified by the inventors, may represent
potential immunogens for use as therapeutic agents or vaccines against
various cancers, and possibly also for use against autoimmune diseases.
In fact, at least one of the agonist peptides appears to be more
immunogenic than the native CAP-1 peptide. CAP-1 antagonists which are
capable of reducing or eliminating this T cell response, such as the
antagonist peptide variant identified by the inventors, may represent
potential agents for use against autoimmune responses to CEA or to
agonist peptide variants thereof.
The prospective exclusive license will be royalty bearing and will
comply with the terms and conditions of 35 U.S.C. 209 and 37 CFR Part
404.7. The prospective 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 establishes that the grant
of the license would not be consistent with the requirements of 35
U.S.C. 209 and 37 CFR Part 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 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: May 1, 2007.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. E7-8888 Filed 5-8-07; 8:45 am]
BILLING CODE 4140-01-P