Government-Owned Inventions; Availability for Licensing, 54578-54580 [2012-21749]
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54578
Federal Register / Vol. 77, No. 172 / Wednesday, September 5, 2012 / Notices
Dated: Board of Governors of the Federal
Reserve System, August 30, 2012.
Margaret Shanks,
Associate Secretary and Ombudsman.
[FR Doc. 2012–21808 Filed 9–4–12; 8:45 am]
[Notice–MA–2012–02; Docket No. 2012–
0004; Sequence 5]
BILLING CODE 6210–01–P
Maximum Per Diem Rates for the
Continental United States (CONUS)
FEDERAL RESERVE SYSTEM
AGENCY:
tkelley on DSK3SPTVN1PROD with NOTICES
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR Part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than September 28,
2012.
A. Federal Reserve Bank of Boston
(Richard Walker, Community Affairs
Officer) P.O. Box 55882, Boston,
Massachusetts 02106–2204:
1. Eastern Bank Corporation, Boston,
Massachusetts, to acquire Campello
Bancorp, and its subsidiary bank, The
Community Bank, A Massachusetts Cooperative Bank, both of Brockton,
Massachusetts.
Dated: Board of Governors of the Federal
Reserve System, August 30, 2012.
Margaret Shanks,
Associate Secretary and Ombudsman.
[FR Doc. 2012–21810 Filed 9–4–12; 8:45 am]
BILLING CODE 6210–01–P
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Office of Governmentwide
Policy (OGP), General Services
Administration (GSA).
ACTION: Notice of GSA Per Diem
Bulletin FTR 13–01, Fiscal Year (FY)
2013 Continental United States
(CONUS) per diem rates.
The General Services
Administration’s (GSA) Fiscal Year (FY)
2013 per diem review has resulted in
lodging and meal allowance changes for
certain locations within the continental
United States (CONUS) to provide for
reimbursement of Federal employees’
expenses covered by per diem. All
current non-standard area (NSA)
lodging per diem rates will remain at FY
2012 levels for FY 2013. The standard
lodging per diem rate of $77 will also
continue to remain the same for FY
2013. The meals and incidental expense
tiers remain unchanged for FY 2013 and
range from $46–$71. GSA identified 10
new NSAs: Bakersfield/Ridgecrest,
California (Kern County); Stockton,
California (San Joaquin County);
Hancock and Pearl River Counties in
Mississippi; Sidney/Glendive, Montana
(Richland and Dawson Counties);
Dickinson/Beulah, North Dakota (Stark,
Mercer, and Billings Counties); Minot,
North Dakota (Ward County); Williston,
North Dakota (Williams, Mountrail, and
McKenzie Counties); Carlsbad, New
Mexico (Eddy County); Watertown, New
York (Jefferson County); and Pasco,
Washington (Franklin County). The
CONUS per diem rates prescribed in
Bulletin 13–01 may be found at
www.gsa.gov/perdiem. GSA bases the
lodging rates on the average daily rate
that the lodging industry reports to an
independent organization. If a lodging
rate or a per diem rate is insufficient to
meet necessary expenses in any given
location, Federal executive agencies can
request that GSA review that location.
Please review numbers five and six of
GSA’s per diem Frequently Asked
Questions at (www.gsa.gov/perdiemfaqs)
for more information on the special
review process.
In addition, the Federal Travel
Regulation allows for actual expense
reimbursement as provided in §§ 301–
11.300 through 301–11.306.
DATES: This notice is effective on
September 5, 2012 and applies for travel
performed on or after October 1, 2012.
SUMMARY:
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For
clarification of content, contact Ms. Jill
Denning, Office of Governmentwide
Policy, Office of Asset and
Transportation Management, at 202–
208–7642, or by email at
travelpolicy@gsa.gov. Please cite Notice
of GSA Per Diem Bulletin FTR 13–01.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
GENERAL SERVICES
ADMINISTRATION
Background
GSA issues and publishes the CONUS
per diem rates, formerly published in
Appendix A to 41 CFR Chapter 301,
solely on the Internet at www.gsa.gov/
perdiem. This process, implemented in
2003, ensures more timely changes in
per diem rates established by GSA for
Federal employees on official travel
within CONUS. Notices published
periodically in the Federal Register,
such as this one, now constitute the
only notification of revisions in CONUS
per diem rates to agencies.
Dated: August 27, 2012.
Janet Dobbs,
Deputy Associate Administrator, Office of
Asset and Transportation Management.
[FR Doc. 2012–21854 Filed 9–4–12; 8:45 am]
BILLING CODE 6820–14–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:
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.
FOR FURTHER INFORMATION: 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.
SUMMARY:
E:\FR\FM\05SEN1.SGM
05SEN1
Federal Register / Vol. 77, No. 172 / Wednesday, September 5, 2012 / Notices
tkelley on DSK3SPTVN1PROD with NOTICES
Enhanced Nanoparticle Cell-Entry for
Cancer Therapy
Description of Technology:
Nanoparticles are being used as a
method of drug delivery for the
treatment of several diseases, cancer in
particular. While the use and versatility
of these particles have increased over
the years, the speed with which these
particles can enter the cells and deliver
the drugs remains challenging.
This technology describes a method of
modifying nanoparticles to markedly
enhance their entry into cancer cells
and their delivery of therapeutic drugs.
The nanoparticles use a multi-shell
calcium phosphate nanocore designed
with target-specific siRNA and an
endocytosis-enhancing agent. The
inventors have shown that the
intravenous systemic administration of
the enhanced nanoparticles noticeably
increases nanoparticle cell-entry along
with concomitant delivery of siRNA to
cancer cells in vivo. They further
demonstrate that the composite calcium
phosphate nanoparticle delivery of anticancer therapy can preferentially target
in vivo tumors and cause tumor growth
arrest. Consequently, these modified
nanoparticles can exert a greater effect
on cancer cells.
Potential Commercial Applications:
• Nanoparticle delivery of therapeutic
treatments to cancers cells.
• Nanoparticle delivery of imaging
agents for the identification and
monitoring of tumor cells.
Competitive Advantages:
• Preferentially taken up by cancer
cells and not normal cells
• Faster uptake into cells than other
nanoparticles
• Tissue and/or cell specific
• Can be customized for targeted
therapy
• Extremely versatile—can transport a
variety of therapeutic agents and the
constructs can incorporate siRNA,
chemotherapy agents, targeted drugs,
pro-drugs, tracers, and radioactive
molecules.
Development Stage:
• In vitro data available
• In vivo data available (animal)
Inventors: King F. Kwong and Lisa A.
Tobin (NCI)
Intellectual Property: HHS Reference
No. E–164–2012/0 — U.S. Patent
Application No. 61/648,735 filed 18
May 2012
Licensing Contact: Whitney Hastings;
301–451–7337; hastingw@mail.nih.gov
Collaborative Research Opportunity:
The Kwong Laboratory, Surgery Branch,
NCI, is seeking statements of capability
or interest from parties interested in
collaborative research to further
VerDate Mar<15>2010
19:14 Sep 04, 2012
Jkt 226001
develop, evaluate or commercialize
nanoparticles in anti-cancer therapy.
For collaboration opportunities, please
contact King F. Kwong, M.D. at
kwongk2@mail.nih.gov.
Therapy for Cancer and Other Diseases
Associated With Angiogenesis Driven
by Vascular Endothelial Growth FactorA
Description of Technology: Vascular
Endothelial Growth Factor-A (VEGF–A)
is an angiogenic agent that drives blood
vessel formation in solid tumors and
other diseases, such as macular
degeneration and diabetic retinopathy.
Several therapies that target the ability
of VEGF to stimulate angiogenesis have
been approved. These therapies regulate
VEGF–A activity by binding VEGF–A,
thereby blocking VEGF–A from binding
to its receptor on target cells. This
technology utilizes a different approach
to regulating VEGF–A activity by
providing a VEGF–A protein antagonist
that is produced by engineering native
VEGF–A protein. The engineered
VEGF–A protein disrupts heparan
sulfate proteoglycan binding to the
VEGF–A/VEGF receptor complex, an
activity that is essential for the
angiogenic properties of native VEGF–
A. The antagonist has a binding affinity
for both FLT–1 (VEGFR–1) and KDR/
FLK–1 (VEGFR–2) that is equivalent to
that of native VEGF–A and specifically
antagonizes all VEGF–A-stimulated
signaling events.
Potential Commercial Applications:
Therapy for solid tumors or other
diseases associated with angiogenic
activity modulated by Vascular
Endothelial Growth Factor-A
expression.
Competitive Advantages:
• Specificity/Selectivity
• Cost-effectiveness in production
Development Stage:
• Early-stage
• In vitro data available
• In vivo data available (animal)
Inventors: Donald P. Bottaro and
Fabiola Cecchi (NCI)
Intellectual Property: HHS Reference
No. E–230–2011/0 — U.S. Patent
Application No. 61/639,230 filed 27 Apr
2012
Licensing Contact: Susan S. Rucker,
CLP; 301–435–4478;
ruckersu@mail.nih.gov
Collaborative Research Opportunity:
The National Cancer Institute’s Urologic
Oncology Branch is seeking statements
of capability or interest from parties
interested in collaborative research to
further develop, evaluate or
commercialize antagonists to VEGF–A
and hepatocyte growth factor (HGF) that
block signal transduction and associated
PO 00000
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54579
cellular responses by competitive
displacement of native growth factors
and concomitant disruption of heparan
sulfate proteoglycan binding to the
growth factor-receptor complex. For
collaboration opportunities, please
contact John Hewes, Ph.D. at
hewesj@mail.nih.gov.
Methods for Identifying and Isolating
Pancreatic Precursor Cells
Description of Technology: Diabetes
results when beta cell performance is
compromised through loss of cells or
reduced cell function. Anti-diabetic
drugs that stimulate insulin production,
such as sulfonylureas and meglitinides,
have limited efficacy when beta cell
responsiveness is deficient. There exists
a critical need for methods to increase
beta cell responsiveness by enhancing
cell function or by increasing beta cell
numbers.
Notch has been shown to play an
important role in pancreas development
and diabetes and NIA investigators
discovered that pancreatic precursor
cells can be identified and isolated
using Notch and its ligands. This
technology describes methods for
identifying pancreatic precursor cells
using a Notch ligand, as well as
methods for isolating pancreatic
precursor cells from a pancreatic cell
sample, such as pancreatic islet cells or
pancreatic extra-islet cells from a
diabetic patient.
Potential Commercial Applications:
• Isolation and expansion of
pancreatic progenitor cells for diabetes
therapy
• Development of a diagnostic test to
monitor beta cell function
Competitive Advantages:
• New diagnostic strategies for
diabetes
• Potential use in regenerative
medicine (pancreatic precursor cells
recently have been shown to have the
potential to develop into other cell
types)
Development Stage:
• Early-stage
• In vitro data available
Inventors: Josephine M. Egan and
Maire Doyle (NIA)
Publication: Kim W, et al. Notch
signaling in pancreatic endocrine cell
and diabetes. Biochem Biophys Res
Commun. 2010 Feb 12;392(3):247–51.
[PMID 20035712]
Intellectual Property: HHS Reference
No. E–262–2003/0 —
• U.S. Provisional Application No.
60/590,281 filed 22 Jul 2004
• PCT Application No. PCT/US2005/
026207 filed 22 Jul 2005, which
published as WO 2006/023209 on 02
Mar 2006
E:\FR\FM\05SEN1.SGM
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54580
Federal Register / Vol. 77, No. 172 / Wednesday, September 5, 2012 / Notices
• U.S. Patent No. 7,888,116 issued 15
Feb 2012
Licensing Contact: Tara L. Kirby,
Ph.D.; 301–435–4426;
tarak@mail.nih.gov
Dated: August 28, 2012.
Richard U. Rodriguez,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 2012–21749 Filed 9–4–12; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
tkelley on DSK3SPTVN1PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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: Healthcare
Delivery and Methodologies Integrated
Review Group, Health Disparities and
Equity Promotion Study Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hotel Monaco Alexandria, 480
King Street, Alexandria, VA 22314.
Contact Person: Delia Olufokunbi
Sam, Ph.D., Scientific Review Officer,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge
Drive, Room 3158, MSC 7770, Bethesda,
MD 20892, 301–435–0684,
olufokunbisamd@csr.nih.gov.
Name of Committee: Surgical
Sciences, Biomedical Imaging and
Bioengineering Integrated Review
Group, Biomedical Imaging Technology
B Study Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Washington Rockville,
1750 Rockville Pike, Rockville, MD
20852.
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19:14 Sep 04, 2012
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Contact Person: Lee Rosen, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room
5116, MSC 7854, Bethesda, MD 20892,
(301) 435–1171. rosenl@csr.nih.gov.
Name of Committee: Immunology
Integrated Review Group,
Hypersensitivity, Autoimmune, and
Immune-mediated Diseases Study
Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Renaissance Washington
Dupont Circle, 1143 New Hampshire
Avenue, Washington, DC 20037.
Contact Person: Bahiru Gametchu,
DVM, Ph.D., Scientific Review Officer,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge
Drive, Room 4204, MSC 7812, Bethesda,
MD 20892, 301–408–9329,
gametchb@csr.nih.gov.
Name of Committee: Cell Biology
Integrated Review Group, Membrane
Biology and Protein Processing Study
Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: One Washington Circle Hotel,
One Washington Circle, Washington, DC
20037.
Contact Person: Janet M Larkin, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room
5142, MSC 7840, Bethesda, MD 20892,
301–806–2765, larkinja@csr.nih.gov.
Name of Committee: Biological
Chemistry and Macromolecular
Biophysics Integrated Review Group,
Biochemistry and Biophysics of
Membranes Study Section.
Date: October 4, 2012.
Time: 8 a.m. to 7 p.m.
Agenda: To review and evaluate grant
applications.
Place: St. Gregory Hotel, 2033 M
Street NW., Washington, DC 20036.
Contact Person: Nuria E. Assa-Munt,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive, Room
4164, MSC 7806, Bethesda, MD 20892,
(301) 451–1323, assamunu@csr.nih.gov.
Name of Committee: Biological
Chemistry and Macromolecular
Biophysics Integrated Review Group,
Macromolecular Structure and Function
C Study Section.
Date: October 4, 2012.
Time: 8 a.m. to 7 p.m.
Agenda: To review and evaluate grant
applications.
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Place: Doubletree Hotel Washington,
1515 Rhode Island Ave. NW.,
Washington, DC 20005.
Contact Person: William A.
Greenberg, Ph.D., Scientific Review
Officer, Center for Scientific Review,
National Institutes of Health, 6701
Rockledge Drive, Room 4168, MSC
7806, Bethesda, MD 20892, (301) 435–
1726, greenbergwa@csr.nih.gov.
Name of Committee: Immunology
Integrated Review Group,
Transplantation, Tolerance, and Tumor
Immunology Study Section.
Date: October 4–5, 2012.
Time: 8a.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: Renaissance Washington,
Dupont Circle, 1143 New Hampshire
Avenue NW., Washington, DC 20037.
Contact Person: Jin Huang, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room
4199, MSC 7812, Bethesda, MD 20892,
301–435–1230, jh377p@nih.gov.
Name of Committee: Musculoskeletal,
Oral and Skin Sciences Integrated
Review Group, Skeletal Biology
Structure and Regeneration Study
Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Daniel F McDonald,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive, Room
4110, MSC 7814, Bethesda, MD 20892,
(301) 435–1215, mcdonald@csr.nih.gov.
Name of Committee: Surgical
Sciences, Biomedical Imaging and
Bioengineering Integrated Review
Group, Biomedical Imaging Technology
A Study Section.
Date: October 4–5, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Washington Rockville,
1750 Rockville Pike, Rockville, MD
20852.
Contact Person: Behrouz Shabestari,
Ph.D., Scientific Review Officer, Center
for Scientific Review, National Institutes
of Health, 6701 Rockledge Drive, Room
5126, MSC 7854, Bethesda, MD 20892,
(301) 435–2409, shabestb@csr.nih.gov.
Name of Committee: Population
Sciences and Epidemiology Integrated
Review Group, Kidney, Nutrition,
Obesity and Diabetes Study Section.
Date: October 4–5, 2012.
E:\FR\FM\05SEN1.SGM
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Agencies
[Federal Register Volume 77, Number 172 (Wednesday, September 5, 2012)]
[Notices]
[Pages 54578-54580]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-21749]
=======================================================================
-----------------------------------------------------------------------
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.
FOR FURTHER INFORMATION: 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.
[[Page 54579]]
Enhanced Nanoparticle Cell-Entry for Cancer Therapy
Description of Technology: Nanoparticles are being used as a method
of drug delivery for the treatment of several diseases, cancer in
particular. While the use and versatility of these particles have
increased over the years, the speed with which these particles can
enter the cells and deliver the drugs remains challenging.
This technology describes a method of modifying nanoparticles to
markedly enhance their entry into cancer cells and their delivery of
therapeutic drugs. The nanoparticles use a multi-shell calcium
phosphate nanocore designed with target-specific siRNA and an
endocytosis-enhancing agent. The inventors have shown that the
intravenous systemic administration of the enhanced nanoparticles
noticeably increases nanoparticle cell-entry along with concomitant
delivery of siRNA to cancer cells in vivo. They further demonstrate
that the composite calcium phosphate nanoparticle delivery of anti-
cancer therapy can preferentially target in vivo tumors and cause tumor
growth arrest. Consequently, these modified nanoparticles can exert a
greater effect on cancer cells.
Potential Commercial Applications:
Nanoparticle delivery of therapeutic treatments to cancers
cells.
Nanoparticle delivery of imaging agents for the
identification and monitoring of tumor cells.
Competitive Advantages:
Preferentially taken up by cancer cells and not normal
cells
Faster uptake into cells than other nanoparticles
Tissue and/or cell specific
Can be customized for targeted therapy
Extremely versatile--can transport a variety of
therapeutic agents and the constructs can incorporate siRNA,
chemotherapy agents, targeted drugs, pro-drugs, tracers, and
radioactive molecules.
Development Stage:
In vitro data available
In vivo data available (animal)
Inventors: King F. Kwong and Lisa A. Tobin (NCI)
Intellectual Property: HHS Reference No. E-164-2012/0 -- U.S.
Patent Application No. 61/648,735 filed 18 May 2012
Licensing Contact: Whitney Hastings; 301-451-7337;
hastingw@mail.nih.gov
Collaborative Research Opportunity: The Kwong Laboratory, Surgery
Branch, NCI, is seeking statements of capability or interest from
parties interested in collaborative research to further develop,
evaluate or commercialize nanoparticles in anti-cancer therapy. For
collaboration opportunities, please contact King F. Kwong, M.D. at
kwongk2@mail.nih.gov.
Therapy for Cancer and Other Diseases Associated With Angiogenesis
Driven by Vascular Endothelial Growth Factor-A
Description of Technology: Vascular Endothelial Growth Factor-A
(VEGF-A) is an angiogenic agent that drives blood vessel formation in
solid tumors and other diseases, such as macular degeneration and
diabetic retinopathy. Several therapies that target the ability of VEGF
to stimulate angiogenesis have been approved. These therapies regulate
VEGF-A activity by binding VEGF-A, thereby blocking VEGF-A from binding
to its receptor on target cells. This technology utilizes a different
approach to regulating VEGF-A activity by providing a VEGF-A protein
antagonist that is produced by engineering native VEGF-A protein. The
engineered VEGF-A protein disrupts heparan sulfate proteoglycan binding
to the VEGF-A/VEGF receptor complex, an activity that is essential for
the angiogenic properties of native VEGF-A. The antagonist has a
binding affinity for both FLT-1 (VEGFR-1) and KDR/FLK-1 (VEGFR-2) that
is equivalent to that of native VEGF-A and specifically antagonizes all
VEGF-A-stimulated signaling events.
Potential Commercial Applications: Therapy for solid tumors or
other diseases associated with angiogenic activity modulated by
Vascular Endothelial Growth Factor-A expression.
Competitive Advantages:
Specificity/Selectivity
Cost-effectiveness in production
Development Stage:
Early-stage
In vitro data available
In vivo data available (animal)
Inventors: Donald P. Bottaro and Fabiola Cecchi (NCI)
Intellectual Property: HHS Reference No. E-230-2011/0 -- U.S.
Patent Application No. 61/639,230 filed 27 Apr 2012
Licensing Contact: Susan S. Rucker, CLP; 301-435-4478;
ruckersu@mail.nih.gov
Collaborative Research Opportunity: The National Cancer Institute's
Urologic Oncology Branch is seeking statements of capability or
interest from parties interested in collaborative research to further
develop, evaluate or commercialize antagonists to VEGF-A and hepatocyte
growth factor (HGF) that block signal transduction and associated
cellular responses by competitive displacement of native growth factors
and concomitant disruption of heparan sulfate proteoglycan binding to
the growth factor-receptor complex. For collaboration opportunities,
please contact John Hewes, Ph.D. at hewesj@mail.nih.gov.
Methods for Identifying and Isolating Pancreatic Precursor Cells
Description of Technology: Diabetes results when beta cell
performance is compromised through loss of cells or reduced cell
function. Anti-diabetic drugs that stimulate insulin production, such
as sulfonylureas and meglitinides, have limited efficacy when beta cell
responsiveness is deficient. There exists a critical need for methods
to increase beta cell responsiveness by enhancing cell function or by
increasing beta cell numbers.
Notch has been shown to play an important role in pancreas
development and diabetes and NIA investigators discovered that
pancreatic precursor cells can be identified and isolated using Notch
and its ligands. This technology describes methods for identifying
pancreatic precursor cells using a Notch ligand, as well as methods for
isolating pancreatic precursor cells from a pancreatic cell sample,
such as pancreatic islet cells or pancreatic extra-islet cells from a
diabetic patient.
Potential Commercial Applications:
Isolation and expansion of pancreatic progenitor cells for
diabetes therapy
Development of a diagnostic test to monitor beta cell
function
Competitive Advantages:
New diagnostic strategies for diabetes
Potential use in regenerative medicine (pancreatic
precursor cells recently have been shown to have the potential to
develop into other cell types)
Development Stage:
Early-stage
In vitro data available
Inventors: Josephine M. Egan and Maire Doyle (NIA)
Publication: Kim W, et al. Notch signaling in pancreatic endocrine
cell and diabetes. Biochem Biophys Res Commun. 2010 Feb 12;392(3):247-
51. [PMID 20035712]
Intellectual Property: HHS Reference No. E-262-2003/0 --
U.S. Provisional Application No. 60/590,281 filed 22 Jul
2004
PCT Application No. PCT/US2005/026207 filed 22 Jul 2005,
which published as WO 2006/023209 on 02 Mar 2006
[[Page 54580]]
U.S. Patent No. 7,888,116 issued 15 Feb 2012
Licensing Contact: Tara L. Kirby, Ph.D.; 301-435-4426;
tarak@mail.nih.gov
Dated: August 28, 2012.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 2012-21749 Filed 9-4-12; 8:45 am]
BILLING CODE 4140-01-P