Government-Owned Inventions; Availability for Licensing, 34024-34025 [E7-11854]
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Federal Register / Vol. 72, No. 118 / Wednesday, June 20, 2007 / Notices
levels of expression are achieved
through use of a specific promoter,
known as CMV/R, in which the Human
T-Lymphotrophic Virus (HTLV–1) Long
Terminal Repeat (LTR) R–U5 region is
substituted for a portion of the intron
downstream of the CMV immediate
early region 1 enhancer (Barouch et al.,
2005). Sequences of 95% or better
homology to CMV/R can be used as
well. CMV/R vectors are currently being
used in a number of clinical trials,
including vaccines against West Nile
Virus, Ebola virus, and HIV and
achieving promising results. The related
HIV vaccine technology is available for
licensing, as is the Ebola DNA vaccine
technology (non-exclusive licensing
only). The CMV/R vector can be used
for any DNA vaccine or for the
production of recombinant proteins in
high yields.
Applications: Vector for DNA
vaccines; High yield expression of
recombinant proteins.
Inventors: Gary Nabel and Zhi-yong
Yang (NIAID).
Patent Status: U.S. Patent No.
7,094,598 issued 22 Aug 2006 [HHS
Reference No. E–241–2001/1–US–01
(CMV/R)], applications pending in EP,
JP, CA, and AU; U.S. Patent Application
No. 10/491,121 filed 23 Aug 2004 [HHS
Reference No. E–241–2001/0–US–07
(Ebola DNA vaccine)], applications
pending in EP, JP, CA, and AU; U.S.
Patent Application No. 11/632,522 filed
16 Jan 2007 [HHS Reference No. E–267–
2004/1–US–08 (HIV DNA vaccine)].
Licensing Status: Available for nonexclusive licensing.
Licensing Contact: Susan Ano, Ph.D.;
301/435–5515; anos@mail.nih.gov.
Dated: June 11, 2007.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E7–11830 Filed 6–19–07; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
rwilkins on PROD1PC63 with NOTICES
AGENCY:
SUMMARY: The inventions listed below
are owned by an agency of the U.S.
Government and are available for
licensing in the U.S. in accordance with
35 U.S.C. 207 to achieve expeditious
VerDate Aug<31>2005
18:25 Jun 19, 2007
Jkt 211001
commercialization of results of
federally-funded research and
development. Foreign patent
applications are filed on selected
inventions to extend market coverage
for companies and may also be available
for licensing.
ADDRESSES: Licensing information and
copies of the U.S. patent applications
listed below may be obtained by writing
to the indicated licensing contact at the
Office of Technology Transfer, National
Institutes of Health, 6011 Executive
Boulevard, Suite 325, Rockville,
Maryland 20852–3804; telephone: 301/
496–7057; fax: 301/402–0220. A signed
Confidential Disclosure Agreement will
be required to receive copies of the
patent applications.
Vibrio Cholerae O139 Conjugate
Vaccines
Description of Technology: Cholera
remains an important public health
problem. Epidemic cholera is caused by
two Vibrio cholerae serotypes O1 and
O139. The disease is spread through
contaminated water. According to
information reported to the World
Health Organization in 1999, nearly
8,500 people died and another 223,000
were sickened with cholera worldwide.
This invention is a polysaccharideprotein conjugate vaccine to prevent
and treat infection by Vibrio cholerae
O139 comprising the capsular
polysaccharide (CPS) of V. cholerae
O139 conjugated through a dicarboxylic
acid dihydrazide linker to a mutant
diphtheria toxin carrier. In addition to
the conjugation methods, also claimed
in the invention are methods of
immunization against V. cholerae O139
using the conjugates of the invention.
The inventors have shown that the
conjugates of the invention elicited in
mice high levels of serum antibodies to
CPS, a surface antigen of Vibrio cholerae
O139, that have vibriocidal activity.
Clinical trials of the two most
immunogenic conjugates have been
planned by the inventors. The conjugate
vaccine is aimed for long lasting
immunity, especially in young children,
and can be administered in concurrent
with routine vaccines.
Inventors: Shousun Szu, Zuzana
Kossaczka, John Robbins (NICHD).
Related Publication: Z Kossaczka et
al. Vibrio cholerae O139 conjugate
vaccines: synthesis and immunogenicity
of V. cholerae O139 capsular
polysaccharide conjugates with
recombinant diphtheria toxin mutant in
mice. Infect Immun. 2000
Sep;68(9):5037–5043.
Patent Status:
PCT Application No. PCT/US00/24119
filed 01 Sep 2000, which published as
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
WO 02/20059 on 14 Mar 2002 (HHS
Reference No. E–274–2000/0–PCT–
01)
U.S. Patent Application No. 10/363,618
filed 01 Sep 2000 (HHS Reference No.
E–274–2000/0–US–02)
U.S. Patent Application No. 11/695,735
filed 03 Apr 2007 (HHS Reference No.
E–274–2000/0–US–03)
Licensing Status: Available for
exclusive or non-exclusive licensing.
Licensing Contact: Peter A. Soukas,
J.D.; 301/435–4646;
soukasp@mail.nih.gov
Collaborative Research Opportunity:
The NICHD/LDMI is seeking statements
of capability or interest from parties
interested in collaborative research to
further develop, evaluate, or
commercialize Vibrio cholera O139 or
O1 conjugate vaccines. Please contact
John D. Hewes, Ph.D. at 301–435–3121
or hewesj@mail.nih.gov for more
information.
CC Chemokine Receptor 5 DNA, New
Animal Models and Therapeutic Agents
for HIV Infection
Description of Technology:
Chemokine receptors are expressed by
many cells, including lymphoid cells,
and function to mediate cell trafficking
and localization. CC chemokine receptor
5 (CCR5) is a seven-transmembrane, G
protein-coupled receptor (GPCR) which
regulates trafficking and effector
functions of memory/effector Tlymphocytes, macrophages, and
immature dendritic cells. Chemokine
binding to CCR5 leads to cellular
activation through pertussis toxinsensitive heterotrimeric G proteins as
well as G protein-independent
signalling pathways. Like many other
GPCRs, CCR5 is regulated by agonistdependent processes which involve G
protein coupled receptor kinase (GRK)dependent phosphorylation, betaarrestin-mediated desensitization and
internalization.
Human CCR5 also functions as the
main coreceptor for the fusion and entry
of many strains of human
immunodeficiency virus (HIV–1, HIV–
2). HIV–1 transmission almost
invariably involves such CCR5-specific
variants (designated R5); individuals
lacking functional CCR5 (by virtue of
homozygosity for a defective CCR5
allele) are almost completely resistant to
HIV–1 infection. Specific blocking of
CCR5 (e.g. with chemokine ligands,
anti-CCR5 antibodies, CCR5-blocking
low MW inhibitors, etc.) inhibits entry/
infection of target cells by R5 HIV
strains. Cells expressing CCR5 and CD4
are useful for screening for agents that
inhibit HIV by binding to CCR5. Such
agents represent potential new
E:\FR\FM\20JNN1.SGM
20JNN1
rwilkins on PROD1PC63 with NOTICES
Federal Register / Vol. 72, No. 118 / Wednesday, June 20, 2007 / Notices
approaches to block HIV transmission
and to treat infected people. A small
animal expressing both human CCR5
along with human CD4 supports entry
of HIV into target cells, a necessary
hurdle that must be overcome for
development of a small animal model
(e.g. transgenic mouse, rat, rabbit, mink)
to study HIV infection and its
inhibition.
The invention embodies the CCR5
genetic sequence, cell lines and
transgenic animals, the cells of which
coexpress human CD4 and CCR5, and
which may represent valuable tools for
the study of HIV infection and for
screening anti-HIV agents. The
invention also embodies anti-CCR5
agents that block HIV env-mediated
membrane fusion associated with HIV
entry into human CD4-positive target
cells or between HIV-infected cells and
uninfected human CD4-positive target
cells.
Inventors: Christophe Combadiere, Yu
Feng, Ghalib Alkahatib, Edward A.
Berger, Philip M. Murphy, Christopher
C. Broder, Paul E. Kennedy (NIAID).
Publication: This technology was
reported in Alkhatib et al., ‘‘CC CKR5:
a RANTES, MIP–1alpha, MIP–1beta
receptor as a fusion cofactor for
macrophage-tropic HIV–1,’’ Science
1996 Jun 28;272(5270):1955–1958.
Patent Status:
U.S. Provisional Application No. 60/
018,508 filed 28 May 1996 (HHS
Reference No. E–090–1996/0–US–01)
U.S. Patent Application No. 08/864,458
filed 28 May 1997 (HHS Reference
No. E–090–1996/0–US–04)
U.S. Patent No. 7,151,087 issued 19 Dec
2006 (HHS Reference No. E–090–
1996/0–US–06)
U.S. Patent Application No. 10/439,845
filed 15 May 2003 (HHS Reference
No. E–090–1996/0–US–05)
U.S. Patent Application No. 10/846,185
filed 14 May 2004 (HHS Reference
No. E–090–1996/0–US–07)
U.S. Patent Application No. 11/594,375
filed 07 Nov 2006 (HHS Reference No.
E–090–1996/0–US–08)
PCT Application No. PCT/US97/09586
filed 28 May 1997 (HHS Reference
No. E–090–1996/0–PCT–02)
European Patent Application No.
97929777.7 filed 28 May 1997 (HHS
Reference No. E–090–1996/0–EP–03)
Licensing Status: The technology is
available for exclusive or nonexclusive
licensing.
Licensing Contact: Peter Soukas; 301/
435–4646; soukasp@mail.nih.gov.
Collaborative Research Opportunity:
The NIAID Laboratory of Molecular
Immunology and Laboratory of Viral
Diseases are seeking statements of
VerDate Aug<31>2005
18:25 Jun 19, 2007
Jkt 211001
capability or interest from parties
interested in collaborative research to
further develop, evaluate, or
commercialize CCR5-related products.
Please contact Philip Murphy (301–496–
8616, pmm@nih.gov) or Edward Berger
(301–402–2481,
edward_berger@nih.gov) for more
information.
Dated: June 11, 2007.
Steven M. Ferguson,
Director,Division of Technology Development
and Transfer,Office of Technology
Transfer,National Institutes of Health.
[FR Doc. E7–11854 Filed 6–19–07; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes on Health
National Institute on Drug Abuse;
Notice of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the following
meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel, Special
Review.
Date: June 28, 2007.
Time: 1:30 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6101
Executive Boulevard, Rockville, MD 20852.
(Telephone Conference Call).
Contact Person: Kesinee Nimit, MD, Health
Scientist Administrator, Office of Extramural
Affairs, National Institute on Drug Abuse,
NIH, DHHS, Room 220, MSC 8401, 6101
Executive Boulevard, Bethesda, MD 20892–
8401, (301) 435–1432.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel,
Pathway to Independence Award.
Date: July 11, 2007.
Time: 1 p.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
34025
Place: National Institutes of Health, 6101
Executive Boulevard, Rockville, MD 20852.
(Telephone Conference Call).
Contact Person: Gerald L. McLaughin, PhD,
Scientific Review Administrator, Office of
Extramural Affairs, National Institute on
Drug Abuse, NIH, DHHS, Room 220, MSC
8401, 6101 Executive Boulevard, Bethesda,
MD 20892–8401, (301) 402–6626.
gm145a@nih.gov.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel, NIDA–
K Conflicts.
Date: July 17, 2007.
Time: 5 p.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: Doubletree Bethesda, 8120
Wisconsin Ave., Bethesda, MD 20814.
Contact Person: Mark Swieter, PhD, Chief,
Training and Special Projects Review Branch,
Office of Extramural Affairs, National
Institute on Drug Abuse, NIH, DHHS, Suite
220, 6101 Executive Boulevard, Bethesda,
MD 20892–8401, (301) 435–1389.
ms80x@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.279, Drug Abuse and
Addiction Research Programs, National
Institutes of Health, HHS).
Dated: June 13, 2007.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 07–3012 Filed 6–19–07; 8:45 am]
BILLING CODE 4140-–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Allergy and
Infectious Diseases; Notice of
ClosedMeetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the following
meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel, T–Cell Immunology.
Date: July 10, 2007.
Time: 11 a.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
E:\FR\FM\20JNN1.SGM
20JNN1
Agencies
[Federal Register Volume 72, Number 118 (Wednesday, June 20, 2007)]
[Notices]
[Pages 34024-34025]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-11854]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The inventions listed below are owned by an agency of the U.S.
Government and are available for licensing in the U.S. in accordance
with 35 U.S.C. 207 to achieve expeditious commercialization of results
of federally-funded research and development. Foreign patent
applications are filed on selected inventions to extend market coverage
for companies and may also be available for licensing.
ADDRESSES: Licensing information and copies of the U.S. patent
applications listed below may be obtained by writing to the indicated
licensing contact at the Office of Technology Transfer, National
Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville,
Maryland 20852-3804; telephone: 301/496-7057; fax: 301/402-0220. A
signed Confidential Disclosure Agreement will be required to receive
copies of the patent applications.
Vibrio Cholerae O139 Conjugate Vaccines
Description of Technology: Cholera remains an important public
health problem. Epidemic cholera is caused by two Vibrio cholerae
serotypes O1 and O139. The disease is spread through contaminated
water. According to information reported to the World Health
Organization in 1999, nearly 8,500 people died and another 223,000 were
sickened with cholera worldwide. This invention is a polysaccharide-
protein conjugate vaccine to prevent and treat infection by Vibrio
cholerae O139 comprising the capsular polysaccharide (CPS) of V.
cholerae O139 conjugated through a dicarboxylic acid dihydrazide linker
to a mutant diphtheria toxin carrier. In addition to the conjugation
methods, also claimed in the invention are methods of immunization
against V. cholerae O139 using the conjugates of the invention. The
inventors have shown that the conjugates of the invention elicited in
mice high levels of serum antibodies to CPS, a surface antigen of
Vibrio cholerae O139, that have vibriocidal activity. Clinical trials
of the two most immunogenic conjugates have been planned by the
inventors. The conjugate vaccine is aimed for long lasting immunity,
especially in young children, and can be administered in concurrent
with routine vaccines.
Inventors: Shousun Szu, Zuzana Kossaczka, John Robbins (NICHD).
Related Publication: Z Kossaczka et al. Vibrio cholerae O139
conjugate vaccines: synthesis and immunogenicity of V. cholerae O139
capsular polysaccharide conjugates with recombinant diphtheria toxin
mutant in mice. Infect Immun. 2000 Sep;68(9):5037-5043.
Patent Status:
PCT Application No. PCT/US00/24119 filed 01 Sep 2000, which published
as WO 02/20059 on 14 Mar 2002 (HHS Reference No. E-274-2000/0-PCT-01)
U.S. Patent Application No. 10/363,618 filed 01 Sep 2000 (HHS Reference
No. E-274-2000/0-US-02)
U.S. Patent Application No. 11/695,735 filed 03 Apr 2007 (HHS Reference
No. E-274-2000/0-US-03)
Licensing Status: Available for exclusive or non-exclusive
licensing.
Licensing Contact: Peter A. Soukas, J.D.; 301/435-4646;
soukasp@mail.nih.gov
Collaborative Research Opportunity: The NICHD/LDMI is seeking
statements of capability or interest from parties interested in
collaborative research to further develop, evaluate, or commercialize
Vibrio cholera O139 or O1 conjugate vaccines. Please contact John D.
Hewes, Ph.D. at 301-435-3121 or hewesj@mail.nih.gov for more
information.
CC Chemokine Receptor 5 DNA, New Animal Models and Therapeutic Agents
for HIV Infection
Description of Technology: Chemokine receptors are expressed by
many cells, including lymphoid cells, and function to mediate cell
trafficking and localization. CC chemokine receptor 5 (CCR5) is a
seven-transmembrane, G protein-coupled receptor (GPCR) which regulates
trafficking and effector functions of memory/effector T-lymphocytes,
macrophages, and immature dendritic cells. Chemokine binding to CCR5
leads to cellular activation through pertussis toxin-sensitive
heterotrimeric G proteins as well as G protein-independent signalling
pathways. Like many other GPCRs, CCR5 is regulated by agonist-dependent
processes which involve G protein coupled receptor kinase (GRK)-
dependent phosphorylation, beta-arrestin-mediated desensitization and
internalization.
Human CCR5 also functions as the main coreceptor for the fusion and
entry of many strains of human immunodeficiency virus (HIV-1, HIV-2).
HIV-1 transmission almost invariably involves such CCR5-specific
variants (designated R5); individuals lacking functional CCR5 (by
virtue of homozygosity for a defective CCR5 allele) are almost
completely resistant to HIV-1 infection. Specific blocking of CCR5
(e.g. with chemokine ligands, anti-CCR5 antibodies, CCR5-blocking low
MW inhibitors, etc.) inhibits entry/infection of target cells by R5 HIV
strains. Cells expressing CCR5 and CD4 are useful for screening for
agents that inhibit HIV by binding to CCR5. Such agents represent
potential new
[[Page 34025]]
approaches to block HIV transmission and to treat infected people. A
small animal expressing both human CCR5 along with human CD4 supports
entry of HIV into target cells, a necessary hurdle that must be
overcome for development of a small animal model (e.g. transgenic
mouse, rat, rabbit, mink) to study HIV infection and its inhibition.
The invention embodies the CCR5 genetic sequence, cell lines and
transgenic animals, the cells of which coexpress human CD4 and CCR5,
and which may represent valuable tools for the study of HIV infection
and for screening anti-HIV agents. The invention also embodies anti-
CCR5 agents that block HIV env-mediated membrane fusion associated with
HIV entry into human CD4-positive target cells or between HIV-infected
cells and uninfected human CD4-positive target cells.
Inventors: Christophe Combadiere, Yu Feng, Ghalib Alkahatib, Edward
A. Berger, Philip M. Murphy, Christopher C. Broder, Paul E. Kennedy
(NIAID).
Publication: This technology was reported in Alkhatib et al., ``CC
CKR5: a RANTES, MIP-1alpha, MIP-1beta receptor as a fusion cofactor for
macrophage-tropic HIV-1,'' Science 1996 Jun 28;272(5270):1955-1958.
Patent Status:
U.S. Provisional Application No. 60/018,508 filed 28 May 1996 (HHS
Reference No. E-090-1996/0-US-01)
U.S. Patent Application No. 08/864,458 filed 28 May 1997 (HHS Reference
No. E-090-1996/0-US-04)
U.S. Patent No. 7,151,087 issued 19 Dec 2006 (HHS Reference No. E-090-
1996/0-US-06)
U.S. Patent Application No. 10/439,845 filed 15 May 2003 (HHS Reference
No. E-090-1996/0-US-05)
U.S. Patent Application No. 10/846,185 filed 14 May 2004 (HHS Reference
No. E-090-1996/0-US-07)
U.S. Patent Application No. 11/594,375 filed 07 Nov 2006 (HHS Reference
No. E-090-1996/0-US-08)
PCT Application No. PCT/US97/09586 filed 28 May 1997 (HHS Reference No.
E-090-1996/0-PCT-02)
European Patent Application No. 97929777.7 filed 28 May 1997 (HHS
Reference No. E-090-1996/0-EP-03)
Licensing Status: The technology is available for exclusive or
nonexclusive licensing.
Licensing Contact: Peter Soukas; 301/435-4646;
soukasp@mail.nih.gov.
Collaborative Research Opportunity: The NIAID Laboratory of
Molecular Immunology and Laboratory of Viral Diseases are seeking
statements of capability or interest from parties interested in
collaborative research to further develop, evaluate, or commercialize
CCR5-related products. Please contact Philip Murphy (301-496-8616,
pmm@nih.gov) or Edward Berger (301-402-2481, edward_berger@nih.gov)
for more information.
Dated: June 11, 2007.
Steven M. Ferguson,
Director,Division of Technology Development and Transfer,Office of
Technology Transfer,National Institutes of Health.
[FR Doc. E7-11854 Filed 6-19-07; 8:45 am]
BILLING CODE 4140-01-P