Government-Owned Inventions; Availability for Licensing, 51835-51836 [06-7329]
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Federal Register / Vol. 71, No. 169 / Thursday, August 31, 2006 / Notices
Covell, WG Rice, E Appella. Synthesis
and biological properties of novel
pyridinioalkanoyl thiolesters (PATE) as
anti-HIV–1 agents that target the viral
nucleocapsid protein zinc fingers. J Med
Chem. 1999 Jan 14;42(1):67–86.
Patent Status: U.S. Patent Application
No. 10/485,165 filed 28 Jan 2004,
claiming priority to 03 Aug 2001 (HHS
Reference No. E–329–2000/0–US–06).
Licensing Status: Available for nonexclusive or exclusive licensing.
Licensing Contact: Sally H. Hu, Ph.D.,
M.B.A.; 301/435–5605;
hus@mail.nih.gov.
Novel Thioesters and Uses Thereof
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Description of Technology: The
human immunodeficiency virus (HIV) is
the causative agent of acquired
immunodeficiency syndrome (AIDS).
Drug-resistance is a critical factor
contributing to the gradual loss of
clinical benefit to treatments for HIV
infection. Accordingly, combination
therapies have further evolved to
address the mutating resistance of HIV.
However, there has been great concern
regarding the apparent growing
resistance of HIV strains to current
therapies.
The present invention provides for a
novel family of thioesters and uses
thereof. These thioesters are capable of
inactivating viruses by a variety of
mechanisms, particularly by
complexing with metal ion-complexing
zinc fingers. The invention further
provides for methods for inactivating a
virus, such as the human
immunodeficiency virus (HIV), using
these compounds, and thereby also
inhibiting transmission of the virus.
Inventors: James A. Turpin (NCI),
Yongsheng Song (NCI), John K. Inman
(NIAID), Mingjun Huang (NCI), Anders
Wallqvist (NCI), David G. Covell (NCI),
William G. Rice (NCI), Ettore Appella
(NCI), et al.
Patent Status: U.S. Patent No.
6,706,729 issued 16 Mar 2004 (HHS
Reference No. E–136–1998/0–US–10);
U.S. Patent Application No. 10/738,062
filed 16 Dec 2003 (HHS Reference No.
E–136–1998/0–US–11).
Licensing Status: Available for nonexclusive or exclusive licensing.
Licensing Contact: Sally H. Hu, Ph.D.,
M.B.A.; 301/435–5605;
hus@mail.nih.gov.
Dated: August 25, 2006.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 06–7327 Filed 8–30–06; 8:45 am]
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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.
A Novel Small Protein Antibiotic
Description of Technology: Due to the
increase in drug resistance among
bacteria, continued progress in the
development of new antibiotic
treatments is needed. Available for
licensing and commercial development
is the small protein SrgT, its analogs
and related peptides. SrgT is a 43 amino
acid protein that effectively inhibits
bacterial growth. This protein likely
exerts its antibiotic action by inhibiting
the metabolism of glucose in these
microorganisms. The claimed invention
includes methods for SrgT synthesis
and suggested modifications for
production of SrgT analogs and related
peptides, which may remain effective
against potential SrgT resistant bacteria.
Thus, the current technology provides a
novel approach to the treatment and
prevention of bacterial infections.
Application: Novel therapeutics and
prophylactics for bacterial infections.
Development Status: Preclinical data
is available at this time.
Inventors: Carin K. Vanderpool and
Susan Gottesman (NCI).
Selected Publication: CK Vanderpool,
S Gottesman. Involvement of a novel
transcriptional activator and small RNA
in post-transcriptional regulation of the
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51835
glucose phosphoenolpyruvate
phosphotransferase system. Mol
Microbiol. 2004 Nov; 54(4):1076–1089.
Patent Status: U.S. Provisional
Application No. 60/799,830 filed 11
May 2006 (HHS Reference No. E–166–
2006/0–US–01).
Licensing Status: Available for nonexclusive and exclusive licensing.
Licensing Contact: Cristina
Thalhammer-Reyero, Ph.D., M.B.A.;
301/435–4507; thalhamc@mail.nih.gov.
Methods and Compositions for the
Production of Highly Effective Vaccines
Against Cancers and Infections
Diseases
Description of Technology: Because
cancers and infectious diseases remain
prominent causes of death among adults
and children worldwide, the availability
of vaccines targeting these conditions is
a global health priority. With the current
vaccine development state-of-the-art,
there are limitless combinations of
enhancing molecules that can be used
with antigen vaccines targeting these
diseases. The technology offered for
licensing and commercial development
combines effective aspects of antigenvaccines, including peptides and other
forms of vaccination, with enhancing
molecules, including co-stimulation of
T cell immunity for efficient vaccine
development.
The claimed invention includes a
non-viral polynucleotide vector
encoding immune enhancing molecules,
such as the T cell co-stimulatory
molecule B7.1 (CD80), which
significantly enhance cellular immune
responses when combined with antigen
stimulation. Delivery of this costimulatory molecule as non-replicating
DNA with any antigenic form, peptides
in this case, overcomes the problems of
combining enhancing molecules with
the antigen in the same DNA vector, coinfecting or transfecting these molecules
in the same antigen presenting or tumor
cell, or manufacturing enhancing
molecules in the same format as the
antigens. Furthermore, the use of this
chimeric vaccine with the enhancing
molecule expressed as polynucleotide
vector overcomes the low antigenicity
and safety considerations of viral
vectors, as well as the instability and
conformational maintenance challenges
associated with the use of full-length
protein delivery. Furthermore,
polynucleotide’s constructs encoding
enhancing molecules are inexpensive to
produce and can potentially be used
along with any form of antigen vaccine
delivery system, including peptides,
full-length proteins and naked DNA
antigens.
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51836
Federal Register / Vol. 71, No. 169 / Thursday, August 31, 2006 / Notices
Applications: (1) Significant
enhancement of immunological
responses to antigen vaccines; (2)
Development of safe and effective
vaccines for cancer and various
infectious diseases; (3) Cost effective
vaccine to test the combination of
immune enhancing molecules with any
form of antigen vaccine.
Development Status: Preclinical data
is available at this time.
Inventors: Samir Khleif and Jay
Berzofsky (NCI).
Patent Status: U.S. Patent Application
No. 09/810,310 filed 14 Mar 2001 (HHS
Reference No. E–128–2000/0-US–02).
Licensing Status: Available for nonexclusive or exclusive licensing.
Licensing Contact: Cristina
Thalhammer-Reyero, Ph.D., M.B.A.;
301/435–4507; thalhamc@mail.nih.gov.
Collaborative Research Opportunity:
The National Cancer Institute Vaccine
Branch is seeking statements of
capability or interest from parties
interested in collaborative research to
further develop, evaluate, or
commercialize methods and
compositions for the production of
highly effective vaccines. Please contact
Betty Tong, Ph.D., at 301–594–4263 or
tongb@mail.nih.gov for more
information.
Dated: August 25, 2006.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 06–7329 Filed 8–30–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, HHS.
AGENCY:
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.
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.
ADDRESSES:
The Mucus Slurper: A Novel Device to
Keep the Endotracheal Tube (ETT) Free
of all Mucus, Without Suctioning.
Description of Technology: Available
for licensing and commercial
development is a mucus slurping device
to remove all mucus, before mucus
reaches the tip of the endotracheal tube
(ETT); thus, no mucus ever enters the
ETT, and the ETT remains always
clean—without suctioning. A
Mallinckrodt Hi-Lo CASS (continuous
aspiration of subglottic secretions)
endotracheal tube is modified by
appending to the distal-most tip of a
cut-off CASS tube a molded, hollow,
concentric plastic ring with 3–4 (or
more) small (less than 1 mm in
diameter) suction ports, the latter
positioned in the most dependent part
of the ETT (Figure 1). The CASS line
was extended to the very tip of the ETT,
and suction was activated for
approximately 0.5 s, synchronized to
the early part of expiration; and
repeated once a minute, or as desired.
All mucus was collected in a small inline vial. Healthy, anesthetized and
paralyzed sheep, were intubated with a
modified 8 mm CASS ETT tube with
attached ‘‘Mucus Slurper’’; with sheep
lying prone, trachea/neck oriented
below horizontal. Never suctioned. At
the end of the 72 h study, sheep were
electively euthanized, and autopsied.
Figure 1. Normal arterial blood gases.
No traces of mucus were found along
the entire length of the ETT. There were
no gross abnormalities of the tracheal
mucosa; Bacterial cultures of the 5 lobes
of the lungs were negative. The Mucus
Slurper represents a new concept that
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may significantly contribute to
improved care of patients intubated and
mechanically ventilated; with no need
for suctioning/cleaning, and free of
ventilator associated pneumonia.
Applications: (1) Prevention of
ventilator associated pneumonia; (2)
Intubation; (3) Mucus clearance.
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Market: All patients intubated for
longer than 18 hours.
Development Status: Pre-clinical data
available from sheep.
Inventors: Theodor Kolobow,
Gianluigi Li Bassi, Francesco Curto
(NHLBI).
Publications:
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]]>Agencies
[Federal Register Volume 71, Number 169 (Thursday, August 31, 2006)]
[Notices]
[Pages 51835-51836]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-7329]
-----------------------------------------------------------------------
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.
A Novel Small Protein Antibiotic
Description of Technology: Due to the increase in drug resistance
among bacteria, continued progress in the development of new antibiotic
treatments is needed. Available for licensing and commercial
development is the small protein SrgT, its analogs and related
peptides. SrgT is a 43 amino acid protein that effectively inhibits
bacterial growth. This protein likely exerts its antibiotic action by
inhibiting the metabolism of glucose in these microorganisms. The
claimed invention includes methods for SrgT synthesis and suggested
modifications for production of SrgT analogs and related peptides,
which may remain effective against potential SrgT resistant bacteria.
Thus, the current technology provides a novel approach to the treatment
and prevention of bacterial infections.
Application: Novel therapeutics and prophylactics for bacterial
infections.
Development Status: Preclinical data is available at this time.
Inventors: Carin K. Vanderpool and Susan Gottesman (NCI).
Selected Publication: CK Vanderpool, S Gottesman. Involvement of a
novel transcriptional activator and small RNA in post-transcriptional
regulation of the glucose phosphoenolpyruvate phosphotransferase
system. Mol Microbiol. 2004 Nov; 54(4):1076-1089.
Patent Status: U.S. Provisional Application No. 60/799,830 filed 11
May 2006 (HHS Reference No. E-166-2006/0-US-01).
Licensing Status: Available for non-exclusive and exclusive
licensing.
Licensing Contact: Cristina Thalhammer-Reyero, Ph.D., M.B.A.; 301/
435-4507; thalhamc@mail.nih.gov.
Methods and Compositions for the Production of Highly Effective
Vaccines Against Cancers and Infections Diseases
Description of Technology: Because cancers and infectious diseases
remain prominent causes of death among adults and children worldwide,
the availability of vaccines targeting these conditions is a global
health priority. With the current vaccine development state-of-the-art,
there are limitless combinations of enhancing molecules that can be
used with antigen vaccines targeting these diseases. The technology
offered for licensing and commercial development combines effective
aspects of antigen-vaccines, including peptides and other forms of
vaccination, with enhancing molecules, including co-stimulation of T
cell immunity for efficient vaccine development.
The claimed invention includes a non-viral polynucleotide vector
encoding immune enhancing molecules, such as the T cell co-stimulatory
molecule B7.1 (CD80), which significantly enhance cellular immune
responses when combined with antigen stimulation. Delivery of this co-
stimulatory molecule as non-replicating DNA with any antigenic form,
peptides in this case, overcomes the problems of combining enhancing
molecules with the antigen in the same DNA vector, co-infecting or
transfecting these molecules in the same antigen presenting or tumor
cell, or manufacturing enhancing molecules in the same format as the
antigens. Furthermore, the use of this chimeric vaccine with the
enhancing molecule expressed as polynucleotide vector overcomes the low
antigenicity and safety considerations of viral vectors, as well as the
instability and conformational maintenance challenges associated with
the use of full-length protein delivery. Furthermore, polynucleotide's
constructs encoding enhancing molecules are inexpensive to produce and
can potentially be used along with any form of antigen vaccine delivery
system, including peptides, full-length proteins and naked DNA
antigens.
[[Page 51836]]
Applications: (1) Significant enhancement of immunological
responses to antigen vaccines; (2) Development of safe and effective
vaccines for cancer and various infectious diseases; (3) Cost effective
vaccine to test the combination of immune enhancing molecules with any
form of antigen vaccine.
Development Status: Preclinical data is available at this time.
Inventors: Samir Khleif and Jay Berzofsky (NCI).
Patent Status: U.S. Patent Application No. 09/810,310 filed 14 Mar
2001 (HHS Reference No. E-128-2000/0-US-02).
Licensing Status: Available for non-exclusive or exclusive
licensing.
Licensing Contact: Cristina Thalhammer-Reyero, Ph.D., M.B.A.; 301/
435-4507; thalhamc@mail.nih.gov.
Collaborative Research Opportunity: The National Cancer Institute
Vaccine Branch is seeking statements of capability or interest from
parties interested in collaborative research to further develop,
evaluate, or commercialize methods and compositions for the production
of highly effective vaccines. Please contact Betty Tong, Ph.D., at 301-
594-4263 or tongb@mail.nih.gov for more information.
Dated: August 25, 2006.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 06-7329 Filed 8-30-06; 8:45 am]
BILLING CODE 4140-01-P
