Government-Owned Inventions; Availability for Licensing, 58862-58863 [E7-20518]
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Federal Register / Vol. 72, No. 200 / Wednesday, October 17, 2007 / Notices
or research reagent antibodies. Please
contact Thomas Stackhouse at
stackhot@mail.nih.gov or 301–846–5465
for more information.
sroberts on PROD1PC70 with NOTICES
Optical Slice Motion Tracker
Description of Technology: Available
for licensing and commercial
development is an apparatus that
adjusts the focal plane of a microscope
in order to track plane motion of a
sample. The apparatus includes a motor
that can change the focal plane by
moving the objective of the microscope
and a computer that reads image data
from the microscope photomultiplier
tube (PMT). The apparatus uses time
between images to perform a navigator
function comprising quickly scanning
many nearby focal planes with a
minimum field of view and utilizing
pattern matching to calculate an offset
distance to adjust the focal plane. The
apparatus permits imaging of moving
structures, such as living tissue, over
time by compensating for motion in the
direction of the focal plane. The use of
navigator movement to track an
optically selected slice can be
implemented in any of various research
or medical devices.
Applications: Microscopy; Cell
biology.
Development Status: Early-stage;
Prototype.
Inventors: James L. Schroeder
(NHLBI), Robert S. Balaban (NHLBI),
Thomas J. Pohida (CIT), John W.
Kakareka (CIT), Randall Pursley (CIT).
Patent Status: U.S. Provisional
Application No. 60/904,683 filed 02 Mar
2007 (HHS Reference No. E–114–2007/
0–US–01). The issued and pending
patent rights are solely owned by the
United States Government.
Licensing Status: Licensing on a nonexclusive basis and exclusive to
qualified applicants whose application
for licensure complies with 37 CFR 404.
Licensing Contact: Michael A.
Shmilovich, Esq.; 301/435–5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity:
The NHLBI is seeking statements of
capability or interest from parties
interested in collaborative research to
further develop, evaluate, or
commercialize the optical slice motion
tracker. Please contact Lili Portilla at
301–594–4273 or via e-mail at
Lilip@nih.gov for more information.
A Fundus Photo-Stimulation System
and Method
Description of Technology: Available
for licensing and commercial
development is an optical system which
permits targeted photo-stimulation of
the retina by positioning the stimulus
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location under visual guidance through
a fundus camera. The system is
designed to elicit, under direct infra-red
visual control of stimulus size and
position in the retina,
electroretinograms (ERGs) in response to
photo-stimulation from selected regions
of the retina, as well as to present small
light stimuli to a selected area to explore
visual sensitivity properties. For
example, the detected ERGs can be the
basis for diagnosing or characterizing
patient retina with early stage retinal
disease versus healthy retina from the
opposite eye. The system can be
mounted on commercially available
fundus cameras that have infra-red
capabilities (or would accept infra-red
bandpass filtering of their retinal
illumination output) and will accept a
near IR CCD camera connected to a TV
mounted on the photographic-camera
port.
The optical system can comprise a
targeting light path originating from a
deep red laser and a stimulus light path
originating from a Xenon strobe lamp.
Both light paths are brought into
collinear alignment by a beam splitter.
The light paths are transmitted to the
eye through an adjustable turning mirror
and a focusing lens. A beam splitter in
front of the fundus camera objective
lens merges the optical path of the
fundus camera with that of the targeting
optical path and the stimulus light path.
The merged beams are brought to a
focus at or close to the lens of the eye.
A movable aperture is interposed on the
collinear beams and imaged on the
retina such that its lateral position and
size can be adjusted by the operator to
select the retinal area to be photostimulated. This arrangement ensures
that the stimulating light flashes
illuminate the same field as was
selected using the deep red targeting
laser. This system permits projection of
repeatable visible-light flashes with
variable size and location onto the
retina.
Applications: Diagnosis of retinal
disease; Electroretinograms.
Development Status: Early-stage;
Prototype available.
Inventors: Paul Smith (ORS), Edward
Wellner (ORS), Francisco de Monasterio
(NEI).
Patent Status: U.S. Provisional
Application No. 60/935,107 filed 26 Jul
2007 (HHS Reference No. E–279–2006/
0–US–01). The pending patent rights are
solely owned by the United States
Government.
Licensing Status: Available for
licensing and commercialization. Nonexclusive rights are available. Exclusive
rights may be available to qualified
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applicants and are subject to the
provisions set forth in 37 CFR 404.7.
Licensing Contact: Michael A.
Shmilovich, Esq.; 301/435–5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity:
The Laboratory of Bioengineering and
Physical Science, NIBIB is seeking
statements of capability or interest from
parties interested in collaborative
research to further develop, evaluate, or
commercialize the Fundus PhotoStimulation System and Method. Please
contact Dr. Paul Smith at
smithpa@mail.nih.gov for more
information.
Dated: October 10, 2007.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E7–20517 Filed 10–16–07; 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.
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
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.
Method for Inducing T-Cell
Proliferation
Description of Technology: This
technology relates to the use of thymic
stromal lymphopoietin (TSLP) to induce
CD4+ T cell proliferation. This
proliferation could be of particular
E:\FR\FM\17OCN1.SGM
17OCN1
Federal Register / Vol. 72, No. 200 / Wednesday, October 17, 2007 / Notices
relevance for patients in whom this cell
population has been significantly
reduced by HIV/AIDS or other
conditions resulting in
immunodeficiency. The proliferation of
isolated CD4+ T cells can be induced
through direct contact with TSLP or a
nucleic acid encoding TSLP. The patent
application also describes methods of
inducing or enhancing an immune
response through administration of
CD4+ T cells that have been isolated
and induced to proliferate using TSLP
or a nucleic acid encoding TSLP. TSLPR
knockout mice are also described in the
patent application and available for
licensing through a biological materials
license agreement.
Applications: Immunotherapy.
Development Status: Animal (mouse)
data available.
Inventor: Warren J. Leonard et al.
(NHLBI).
Patent Status: U.S. Provisional
Application No. 60/555,898 filed 23 Mar
2004 (HHS Reference No. E–104–2004/
0–US–01); U.S. Utility Application No.
11/762,357 filed 13 June 2007 (HHS
Reference No. E–104–2004/1–US–02).
Licensing Status: Available for
licensing.
Licensing Contact: Susan Ano, Ph.D.;
301/435–5515; anos@mail.nih.gov.
sroberts on PROD1PC70 with NOTICES
Retrovirus-Like Particles as Vaccines
and Immunogens
Description of Technology: This
technology describes retrovirus-like
particles and their production from
retroviral constructs in which the gene
encoding of all but seven amino acids of
the nucleocapsid (NC) protein was
deleted. NC is critical for both genomic
RNA packaging into the virion and viral
integration into the host cell. Therefore,
this deletion functionally eliminates
two essential steps in retrovirus
replication, thereby resulting in noninfectious retrovirus-like particles that
maintain their full complement of
antigenic proteins. Furthermore,
efficient formation of these particles
requires inhibition of the protease
enzymatic activity, either by mutation to
the protease gene in the construct or by
protease inhibitor thereby ensuring the
production of non-infectious retroviruslike particles by altering two
independent targets. These particles can
be used in vaccines or immunogenic
compositions. Specific examples using
HIV–1 constructs are given.
Applications: Retroviral vaccine;
Immunogenic compositions.
Development Status: In vitro data
available.
Inventor: David E. Ott (NCI).
Publications:
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19:05 Oct 16, 2007
Jkt 214001
1. DE Ott et al. Elimination of protease
activity restores efficient virion
production to a human
immunodeficiency virus type 1
nucleocapsid deletion mutant. J Virol.
2003 May;77(10):5547–5556.
2. DE Ott et al. Redundant roles for
nucleocapsid and matrix RNA-binding
sequences in human immunodeficiency
virus type 1 assembly. J Virol. 2005
Nov;79(22), 13839–13847.
Patent Status: U.S. Patent Application
No. 11/413,614 filed 27 Apr 2006 (HHS
Reference No. E–236–2003/0–US–02).
Licensing Status: Available for nonexclusive or exclusive licensing.
Licensing Contact: Susan Ano, Ph.D.;
301/435–5515; anos@mail.nih.gov.
Collaborative Research Opportunity:
The NCI, CCR, AIDS Vaccine Program is
seeking statements of capability or
interest from parties interested in
collaborative research to further
develop, evaluate, or commercialize
whole retrovirus-like particle vaccines.
Please contact John D. Hewes, Ph.D. at
301–435–3121 or hewesj@mail.nih.gov
for more information.
Potent HIV–1 Entry Inhibitors and
Immunogens
Description of Technology: This
technology relates to HIV antigenic
constructs with flexible, heterologous
linkers joining gp120 and gp41. The
HIV–1 envelope Glycoprotein (Env)
undergoes conformational changes
while driving entry. The inventors
developed these constructs to mimic
some of the intermediate Env
conformations. Tethered molecules of
the invention were stable and potently
inhibited cell fusion. Both gp120 and
gp41 contain epitopes that may be
necessary for the immune system to
mount a robust and effective immune
response to HIV. By connecting the two
components, the current invention
stabilizes the exposure of conserved
epitopes, thereby increasing the chances
that antibodies will form that react with
these sites.
Applications: HIV vaccine.
Development Status: In vitro data
available.
Inventors: Dimiter S. Dimitrov et al.
(NCI).
Patent Status: U.S. Utility Application
No. 10/506,651 filed 02 Sept 2004 (HHS
Reference No. E–039–2002/0–US–02).
Licensing Status: Available for
exclusive or non-exclusive licensing.
Licensing Contact: Susan Ano, Ph.D.;
301/435–5515; anos@mail.nih.gov.
Collaborative Research Opportunity:
The National Cancer Institute’s
Nanobiology Program is seeking
statements of capability or interest from
parties interested in collaborative
PO 00000
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Fmt 4703
Sfmt 4703
58863
research to further develop or evaluate
immune response constructs. Please
contact John D. Hewes, Ph.D. at 301–
435–3121 or hewesj@mail.nih.gov for
more information.
Dated: October 10, 2007.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E7–20518 Filed 10–16–07; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive
License: Adult Human Dental Pulp
Stem Cells, Postnatal Stem Cells, and
Multipotent Postnatal Stem Cells From
Human Periodontal Ligament
National Institutes of Health,
Public Health Service, HHS.
AGENCY:
ACTION:
Notice.
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 (NIH), Department
of Health and Human Services (HHS), is
contemplating the grant of an exclusive
license worldwide to practice the
invention embodied in United States
issued Patent Number 7,052,907 titled:
‘‘Adult Human Dental Pulp Stem Cells
in vitro and in vivo’’ referenced at HHS
as E–233–2000/0–US–03 and
corresponding foreign patent
applications, United States Patent
Application Number 10/553,633 titled:
‘‘Postnatal Stem Cells and Uses
Thereof’’ referenced at HHS as E–018–
2003/0–US–02 and corresponding
foreign patent applications, United
States Patent Application Number 11/
433,627 titled: ‘‘Multipotent Postnatal
Stem Cells from Human Periodontal
Ligament’’ referenced at DHHS as E–
033–2004/0–US–03 and corresponding
patent applications, to Angioblast
Systems, Inc. having a place of business
in the state of New York. The field of
use may be limited to the following:
FDA or similar foreign body approved
therapeutic for (1) regeneration/repair of
the periodontal ligament lost from
chronic periodontitis, (2) regeneration/
repair of dentin/pulp complex lost
during deep carious lesions and (3)
regeneration/repair of neural networks.
The United States of America is the
assignee of the patent rights in this
invention. The territory may be
worldwide.
E:\FR\FM\17OCN1.SGM
17OCN1
Agencies
[Federal Register Volume 72, Number 200 (Wednesday, October 17, 2007)]
[Notices]
[Pages 58862-58863]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-20518]
-----------------------------------------------------------------------
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.
Method for Inducing T-Cell Proliferation
Description of Technology: This technology relates to the use of
thymic stromal lymphopoietin (TSLP) to induce CD4+ T cell
proliferation. This proliferation could be of particular
[[Page 58863]]
relevance for patients in whom this cell population has been
significantly reduced by HIV/AIDS or other conditions resulting in
immunodeficiency. The proliferation of isolated CD4+ T cells can be
induced through direct contact with TSLP or a nucleic acid encoding
TSLP. The patent application also describes methods of inducing or
enhancing an immune response through administration of CD4+ T cells
that have been isolated and induced to proliferate using TSLP or a
nucleic acid encoding TSLP. TSLPR knockout mice are also described in
the patent application and available for licensing through a biological
materials license agreement.
Applications: Immunotherapy.
Development Status: Animal (mouse) data available.
Inventor: Warren J. Leonard et al. (NHLBI).
Patent Status: U.S. Provisional Application No. 60/555,898 filed 23
Mar 2004 (HHS Reference No. E-104-2004/0-US-01); U.S. Utility
Application No. 11/762,357 filed 13 June 2007 (HHS Reference No. E-104-
2004/1-US-02).
Licensing Status: Available for licensing.
Licensing Contact: Susan Ano, Ph.D.; 301/435-5515;
anos@mail.nih.gov.
Retrovirus-Like Particles as Vaccines and Immunogens
Description of Technology: This technology describes retrovirus-
like particles and their production from retroviral constructs in which
the gene encoding of all but seven amino acids of the nucleocapsid (NC)
protein was deleted. NC is critical for both genomic RNA packaging into
the virion and viral integration into the host cell. Therefore, this
deletion functionally eliminates two essential steps in retrovirus
replication, thereby resulting in non-infectious retrovirus-like
particles that maintain their full complement of antigenic proteins.
Furthermore, efficient formation of these particles requires inhibition
of the protease enzymatic activity, either by mutation to the protease
gene in the construct or by protease inhibitor thereby ensuring the
production of non-infectious retrovirus-like particles by altering two
independent targets. These particles can be used in vaccines or
immunogenic compositions. Specific examples using HIV-1 constructs are
given.
Applications: Retroviral vaccine; Immunogenic compositions.
Development Status: In vitro data available.
Inventor: David E. Ott (NCI).
Publications:
1. DE Ott et al. Elimination of protease activity restores
efficient virion production to a human immunodeficiency virus type 1
nucleocapsid deletion mutant. J Virol. 2003 May;77(10):5547-5556.
2. DE Ott et al. Redundant roles for nucleocapsid and matrix RNA-
binding sequences in human immunodeficiency virus type 1 assembly. J
Virol. 2005 Nov;79(22), 13839-13847.
Patent Status: U.S. Patent Application No. 11/413,614 filed 27 Apr
2006 (HHS Reference No. E-236-2003/0-US-02).
Licensing Status: Available for non-exclusive or exclusive
licensing.
Licensing Contact: Susan Ano, Ph.D.; 301/435-5515;
anos@mail.nih.gov.
Collaborative Research Opportunity: The NCI, CCR, AIDS Vaccine
Program is seeking statements of capability or interest from parties
interested in collaborative research to further develop, evaluate, or
commercialize whole retrovirus-like particle vaccines. Please contact
John D. Hewes, Ph.D. at 301-435-3121 or hewesj@mail.nih.gov for more
information.
Potent HIV-1 Entry Inhibitors and Immunogens
Description of Technology: This technology relates to HIV antigenic
constructs with flexible, heterologous linkers joining gp120 and gp41.
The HIV-1 envelope Glycoprotein (Env) undergoes conformational changes
while driving entry. The inventors developed these constructs to mimic
some of the intermediate Env conformations. Tethered molecules of the
invention were stable and potently inhibited cell fusion. Both gp120
and gp41 contain epitopes that may be necessary for the immune system
to mount a robust and effective immune response to HIV. By connecting
the two components, the current invention stabilizes the exposure of
conserved epitopes, thereby increasing the chances that antibodies will
form that react with these sites.
Applications: HIV vaccine.
Development Status: In vitro data available.
Inventors: Dimiter S. Dimitrov et al. (NCI).
Patent Status: U.S. Utility Application No. 10/506,651 filed 02
Sept 2004 (HHS Reference No. E-039-2002/0-US-02).
Licensing Status: Available for exclusive or non-exclusive
licensing.
Licensing Contact: Susan Ano, Ph.D.; 301/435-5515;
anos@mail.nih.gov.
Collaborative Research Opportunity: The National Cancer Institute's
Nanobiology Program is seeking statements of capability or interest
from parties interested in collaborative research to further develop or
evaluate immune response constructs. Please contact John D. Hewes,
Ph.D. at 301-435-3121 or hewesj@mail.nih.gov for more information.
Dated: October 10, 2007.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. E7-20518 Filed 10-16-07; 8:45 am]
BILLING CODE 4140-01-P