Government-Owned Inventions; Availability for Licensing, 66788-66789 [E6-19408]
Download as PDF
<![CDATA[
66788
Federal Register / Vol. 71, No. 221 / Thursday, November 16, 2006 / Notices
Proposed Project: Health Resources and
Services Administration Core Clinical
Measures Implementation Feasibility
Study
In response to the Health and Human
Service’s Department-wide objectives
and HRSA’s strategic goals, a set of core
clinical performance measures have
been established. These measures will
assist in the evaluation of HRSA
program performance in defined clinical
areas to facilitate quality improvement
activities for HRSA and its grantees. The
purpose of the proposed voluntary
feasibility study is to learn from HRSA’s
health service delivery grantees, which
have different reporting capacities,
about their abilities to report national
standardized measures. More
specifically, the study will help HRSA
to understand: (1) The factors involved
in the HRSA grantee decision making
processes around measure selection/
choice; (2) Grantees’ data collection
capacity including tools, processes and
infrastructure; (3) Level of grantee effort
involved in measure reporting; and (4)
How the performance process will
impact the grantees’ quality
improvement efforts. Overall the
feasibility study will allow HRSA to
query its grantees related to the newly
Responses
per
respondent
Number of
respondents
introduced core clinical performance
measure set.
The feasibility study includes the
actual data collection of the proposed
clinical measures along with a report
form to assess burden, data collection
and reporting capacity, and technical
assistance needs. Additionally, the
study will provide HRSA with the
opportunity to refine instructions and
performance measure definitions
accordingly in preparation for the actual
implementation of the clinical
measures.
The estimated annualized response
burden is as follows:
Total
responses
Hours per
response
Total hour
burden
Clinical Measures ...............................................................
Report Form .......................................................................
50
50
1
1
50
50
40
1.5
2,000
75
Total ............................................................................
50
........................
50
..........................
2075
Send comments to Susan G. Queen,
Ph.D., HRSA Reports Clearance Officer,
Room 10–33, Parklawn Building, 5600
Fishers Lane, Rockville, MD 20857.
Written comments should be received
within 60 days of this notice.
Dated: November 8, 2006.
Cheryl R. Dammons,
Director, Division of Policy Review and
Coordination.
[FR Doc. E6–19377 Filed 11–15–06; 8:45 am]
BILLING CODE 4165–15–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.
pwalker on PROD1PC61 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
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
VerDate Aug<31>2005
20:27 Nov 15, 2006
Jkt 211001
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.
Second Generation Nitric OxideReleasing Non-Steroidal AntiInflammatory Drugs Possessing a
Diazeniumdiolate Group (NONO–
NSAIDs)
Description of Technology: Nonsteroidal anti-inflammatory drugs
(NSAIDs) are one of the most useful
clinical therapies for the treatment of
pain, fever and inflammation. It is
estimated that more than 30 million
people take NSAIDs every day.
However, the major mechanism by
which NSAIDs exert their antiinflammatory activity is also responsible
for the gastrointestinal, renal and
hepatic side effects observed in patients
undergoing long-term treatment of
chronic conditions. The most common
side effects associated with NSAID
administration are gastroduodenal
erosions and ulcerations affecting
around 15% of chronic NSAID users.
While many of these clinical
manifestations are mild, they may
develop into serious events such as
bleeding, perforation, obstruction, and
sudden death. Therefore, the gastric
irritant effect of NSAIDs (particularly
aspirin) can be a deterrent to its longterm use for the prophylactic prevention
of adverse cardiovascular events such as
stroke and myocardial infarction, or as
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
a safe chemopreventive agent to avoid
the recurrence of colorectal cancer
(CRC).
One of the main strategies that have
emerged to improve the safety profile of
NSAIDs is the linkage of a nitric oxide
(NO)-releasing moiety to the structure of
classical NSAIDs (NO–NSAIDs).
However, all NO-releasing NSAIDs
published so far have a nitrooxyalkyl
group as the NO-releasing group. An
important drawback to this design is the
fact that production of NO (only one
equivalent) from organic nitrate esters
requires a metabolic three-electron
reduction in vivo, and this activation
decreases in efficiency on continued use
of the drugs, contributing to ‘‘nitrate
tolerance’’.
This invention describes the design,
synthesis and biological evaluation of
novel NO-releasing non-steroidal antiinflammatory prodrugs (NONO–
NSAIDs) possessing a N-diazen-1-ium1,2-diolate (NONOate), which offers
additional advantages compared with
organic nitrate-based NO–NSAIDs:
(a) Simultaneous release of the
corresponding NSAID and NO.
(b) Production of two equivalents of
NO (twice as much) by a first-order rate.
(c) Metabolic activation (hydrolysis)
mediated by non-specific esterases,
which unlike redox metabolism, is not
expected to produce tolerance upon
long-term treatment.
Applications: This invention provides
a group of anti-inflammatory, analgesic,
and gastrointestinal safe prodrugs,
which are expected to be a suitable
alternative for the prophylactic
prevention of adverse cardiovascular
E:\FR\FM\16NON1.SGM
16NON1
Federal Register / Vol. 71, No. 221 / Thursday, November 16, 2006 / Notices
pwalker on PROD1PC61 with NOTICES
events such as stroke and myocardial
infarction, as well as cancer
chemoprevention.
Market: (1) An estimated 60 million
people in the United States use NSAIDs
regularly; (2) An estimated $5 billion are
spent each year in the United States on
prescription NSAIDs and approximately
$2 billion are spent on over-the-counter
NSAIDs.
Development Status: Pre-clinical data
is available.
Inventors: Carlos Velazquez Martinez
(NCI) et al.
Related Publication: C Velazquez, PN
Praveen Rao, EE Knaus. Novel
nonsteroidal anti-inflammatory drugs
possessing a nitric oxide donor diazen1-ium-1,2-diolate moiety: Design,
synthesis, biological evaluation, and
nitric oxide release studies. J Med
Chem. 2005 Jun16;48(12):4061–4067.
Patent Status: U.S. Provisional
Application 60/794,421 filed 24 Apr
2006 (HHS Reference No. E–186–2006/
0–US–01).
Licensing Status: Available for
exclusive and non-exclusive licensing.
Licensing Contact: Norbert Pontzer,
PhD, J.D.; 301/435–5502;
pontzern@mail.nih.gov.
Collaborative Research Opportunity:
The Chemistry Section of the Laboratory
of Comparative Carcinogenesis is
seeking statements of capability or
interest from parties interested in
collaborative research to further
develop, evaluate, or commercialize the
prodrugs described, as new and safer
analgesic, anti-inflammatory, antithrombotic, and cancer
chemopreventive agents. Please contact
Betty Tong, Ph.D. at 301–594–4263 or
tongb@mail.nih.gov for more
information.
Rat or Mouse Exhibiting Behaviors
Associated With Human Schizophrenia
Description of Technology: A newly
developed animal model for
schizophrenia is valuable for assaying
pharmaceutical compounds for treating
this disorder. Schizophrenia is a
neuropsychiatric disorder characterized
by cognitive deficits, bizarre behavior
and/or hallucinations. Presently, there
has been no satisfactory animal model
for testing promising therapies for this
disorder.
This invention provides a unique and
surprisingly accurate animal model for
human schizophrenia. The animals are
brain damaged while prepubescent. The
brain damage consists of a ventral
hippocampus lesion induced by
exposure of the hippocampus region to
a neurotoxin. When the animal reaches
puberty, abnormal behavior and a
number of biological phenomena
VerDate Aug<31>2005
20:27 Nov 15, 2006
Jkt 211001
associated with schizophrenic
symptoms emerge.
The present invention also provides
methods of assaying the antischizophrenic potential of
pharmaceutical compositions. The
methods involve (a) Inducing or creating
a lesion in the ventral hippocampus of
a prepubescent mammal, (b) nurturing
or raising the mammal until
postpuberty, (c) administering to the
mammal a pharmaceutical composition
thought to have anti-schizophrenic
properties; and (d) determining the
mammal’s response to the
pharmaceutical composition. The antischizophrenic potential of the
pharmaceutical composition is assessed
by objectively measuring the mammal’s
behavior following administration of the
pharmaceutical composition. The
behaviors which are measured typically
include the following: locomotor
activity in a cage, in unfamiliar or novel
environments, after injection or
administration of drugs (e.g.,
amphetamines), after mild electric
shock, after exposure to sensory stimuli
(e.g., noise), in water (swim test), after
immobilization, in social interactions,
and in various learning and reward
paradigms.
The neurotoxin used can be selected
from a number of known agents which
lethally affect neurons usually, but not
exclusively, by over-exciting their
glummate receptors. Examples of such
neurotoxins include ibotenic acid, Nmethyl-D-aspartic acid, kainic acid,
dihydrokainate, DL-homocysteate, Lcysteate, L-aspartate, L-glutamate,
colchicine, ferric chloride, omegaconotoxin GVIA, 6-hydroxy-dopamine.
Advantage: This is the first model
showing postpubertal emergence of
abnormalities similar to those reported
in schizophrenia.
Applications: (1) Animal model for
human schizophrenia; (2) Screening
methods for Anti-schizophrenics.
Development Status: Validated, well
characterized and ready for use.
Inventors: Daniel R. Weinberger,
Barbara K. Lipska, and George E. Jaskiw
(NIMH).
Publications:
1. AHC Wong, BK Lipska, O Likhodi,
E Boffa, DR Weinberger, JL Kennedy,
HHM Van Tol. Cortical gene expression
in the neonatal ventral-hippocampal
lesion rat model. Schizophr Res. 2005
Sep 15;77(2–3):261–270.
2. BK Lipska. Using animal models to
test a neurodevelopmental hypothesis of
schizophrenia. J Psychiatry Neurosci.
2004 Jul;29(4):282–286.
3. BK Lipska and DR Weinberger. To
model a psychiatric disorder in animals:
schizophrenia as a reality test.
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
66789
Neuropsychopharmacology 2000
Sep;23(3):223–239.
4. BK Lipska, GE Jaskiw, DR
Weinberger. Postpubertal emergence of
hyperresponsiveness to stress and to
amphetamine after neonatal excitotoxic
damage: a potential animal model of
schizophrenia.
Neuropsychopharmacology 1993
Aug;9(1):67–75.
Patent Status: U.S. Patent No.
5,549,884 issued 27 Aug 1996 (HHS
Reference No. E–013–1993/0–US–01).
Availability: Available for nonexclusive licensing.
Licensing Contact: Norbert Pontzer,
Ph.D., J.D.; 301/435–5502;
pontzern@mail.nih.gov.
Dated: November 8, 2006.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E6–19408 Filed 11–15–06; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Human Genome Research
Institute; Notice of Closed Meeting
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
meeting.
The meeting 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
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 Human
Genome Research Institute Special Emphasis
Panel; ENCODE RFA.
Date: December 6–7, 2006.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: The Watergate, 2650 Virginia
Avenue, NW., Washington, DC 20037.
Contact Person: Rudy O. Pozzatti, PhD,
Scientific Review Administrator, Office of
Scientific Review, National Human Genome
Research Institute, National Institutes of
Health, Bethesda, MD 20892, 301 402–0838.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.172, Human Genome
Research, National Institutes of Health, HHS)
E:\FR\FM\16NON1.SGM
16NON1
]]>Agencies
[Federal Register Volume 71, Number 221 (Thursday, November 16, 2006)]
[Notices]
[Pages 66788-66789]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-19408]
-----------------------------------------------------------------------
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.
Second Generation Nitric Oxide-Releasing Non-Steroidal Anti-
Inflammatory Drugs Possessing a Diazeniumdiolate Group (NONO-NSAIDs)
Description of Technology: Non-steroidal anti-inflammatory drugs
(NSAIDs) are one of the most useful clinical therapies for the
treatment of pain, fever and inflammation. It is estimated that more
than 30 million people take NSAIDs every day. However, the major
mechanism by which NSAIDs exert their anti-inflammatory activity is
also responsible for the gastrointestinal, renal and hepatic side
effects observed in patients undergoing long-term treatment of chronic
conditions. The most common side effects associated with NSAID
administration are gastroduodenal erosions and ulcerations affecting
around 15% of chronic NSAID users. While many of these clinical
manifestations are mild, they may develop into serious events such as
bleeding, perforation, obstruction, and sudden death. Therefore, the
gastric irritant effect of NSAIDs (particularly aspirin) can be a
deterrent to its long-term use for the prophylactic prevention of
adverse cardiovascular events such as stroke and myocardial infarction,
or as a safe chemopreventive agent to avoid the recurrence of
colorectal cancer (CRC).
One of the main strategies that have emerged to improve the safety
profile of NSAIDs is the linkage of a nitric oxide (NO)-releasing
moiety to the structure of classical NSAIDs (NO-NSAIDs). However, all
NO-releasing NSAIDs published so far have a nitrooxyalkyl group as the
NO-releasing group. An important drawback to this design is the fact
that production of NO (only one equivalent) from organic nitrate esters
requires a metabolic three-electron reduction in vivo, and this
activation decreases in efficiency on continued use of the drugs,
contributing to ``nitrate tolerance''.
This invention describes the design, synthesis and biological
evaluation of novel NO-releasing non-steroidal anti-inflammatory
prodrugs (NONO-NSAIDs) possessing a N-diazen-1-ium-1,2-diolate
(NONOate), which offers additional advantages compared with organic
nitrate-based NO-NSAIDs:
(a) Simultaneous release of the corresponding NSAID and NO.
(b) Production of two equivalents of NO (twice as much) by a first-
order rate.
(c) Metabolic activation (hydrolysis) mediated by non-specific
esterases, which unlike redox metabolism, is not expected to produce
tolerance upon long-term treatment.
Applications: This invention provides a group of anti-inflammatory,
analgesic, and gastrointestinal safe prodrugs, which are expected to be
a suitable alternative for the prophylactic prevention of adverse
cardiovascular
[[Page 66789]]
events such as stroke and myocardial infarction, as well as cancer
chemoprevention.
Market: (1) An estimated 60 million people in the United States use
NSAIDs regularly; (2) An estimated $5 billion are spent each year in
the United States on prescription NSAIDs and approximately $2 billion
are spent on over-the-counter NSAIDs.
Development Status: Pre-clinical data is available.
Inventors: Carlos Velazquez Martinez (NCI) et al.
Related Publication: C Velazquez, PN Praveen Rao, EE Knaus. Novel
nonsteroidal anti-inflammatory drugs possessing a nitric oxide donor
diazen-1-ium-1,2-diolate moiety: Design, synthesis, biological
evaluation, and nitric oxide release studies. J Med Chem. 2005
Jun16;48(12):4061-4067.
Patent Status: U.S. Provisional Application 60/794,421 filed 24 Apr
2006 (HHS Reference No. E-186-2006/0-US-01).
Licensing Status: Available for exclusive and non-exclusive
licensing.
Licensing Contact: Norbert Pontzer, PhD, J.D.; 301/435-5502;
pontzern@mail.nih.gov.
Collaborative Research Opportunity: The Chemistry Section of the
Laboratory of Comparative Carcinogenesis is seeking statements of
capability or interest from parties interested in collaborative
research to further develop, evaluate, or commercialize the prodrugs
described, as new and safer analgesic, anti-inflammatory, anti-
thrombotic, and cancer chemopreventive agents. Please contact Betty
Tong, Ph.D. at 301-594-4263 or tongb@mail.nih.gov for more information.
Rat or Mouse Exhibiting Behaviors Associated With Human Schizophrenia
Description of Technology: A newly developed animal model for
schizophrenia is valuable for assaying pharmaceutical compounds for
treating this disorder. Schizophrenia is a neuropsychiatric disorder
characterized by cognitive deficits, bizarre behavior and/or
hallucinations. Presently, there has been no satisfactory animal model
for testing promising therapies for this disorder.
This invention provides a unique and surprisingly accurate animal
model for human schizophrenia. The animals are brain damaged while
prepubescent. The brain damage consists of a ventral hippocampus lesion
induced by exposure of the hippocampus region to a neurotoxin. When the
animal reaches puberty, abnormal behavior and a number of biological
phenomena associated with schizophrenic symptoms emerge.
The present invention also provides methods of assaying the anti-
schizophrenic potential of pharmaceutical compositions. The methods
involve (a) Inducing or creating a lesion in the ventral hippocampus of
a prepubescent mammal, (b) nurturing or raising the mammal until
postpuberty, (c) administering to the mammal a pharmaceutical
composition thought to have anti-schizophrenic properties; and (d)
determining the mammal's response to the pharmaceutical composition.
The anti-schizophrenic potential of the pharmaceutical composition is
assessed by objectively measuring the mammal's behavior following
administration of the pharmaceutical composition. The behaviors which
are measured typically include the following: locomotor activity in a
cage, in unfamiliar or novel environments, after injection or
administration of drugs (e.g., amphetamines), after mild electric
shock, after exposure to sensory stimuli (e.g., noise), in water (swim
test), after immobilization, in social interactions, and in various
learning and reward paradigms.
The neurotoxin used can be selected from a number of known agents
which lethally affect neurons usually, but not exclusively, by over-
exciting their glummate receptors. Examples of such neurotoxins include
ibotenic acid, N-methyl-D-aspartic acid, kainic acid, dihydrokainate,
DL-homocysteate, L-cysteate, L-aspartate, L-glutamate, colchicine,
ferric chloride, omega-conotoxin GVIA, 6-hydroxy-dopamine.
Advantage: This is the first model showing postpubertal emergence
of abnormalities similar to those reported in schizophrenia.
Applications: (1) Animal model for human schizophrenia; (2)
Screening methods for Anti-schizophrenics.
Development Status: Validated, well characterized and ready for
use.
Inventors: Daniel R. Weinberger, Barbara K. Lipska, and George E.
Jaskiw (NIMH).
Publications:
1. AHC Wong, BK Lipska, O Likhodi, E Boffa, DR Weinberger, JL
Kennedy, HHM Van Tol. Cortical gene expression in the neonatal ventral-
hippocampal lesion rat model. Schizophr Res. 2005 Sep 15;77(2-3):261-
270.
2. BK Lipska. Using animal models to test a neurodevelopmental
hypothesis of schizophrenia. J Psychiatry Neurosci. 2004 Jul;29(4):282-
286.
3. BK Lipska and DR Weinberger. To model a psychiatric disorder in
animals: schizophrenia as a reality test. Neuropsychopharmacology 2000
Sep;23(3):223-239.
4. BK Lipska, GE Jaskiw, DR Weinberger. Postpubertal emergence of
hyperresponsiveness to stress and to amphetamine after neonatal
excitotoxic damage: a potential animal model of schizophrenia.
Neuropsychopharmacology 1993 Aug;9(1):67-75.
Patent Status: U.S. Patent No. 5,549,884 issued 27 Aug 1996 (HHS
Reference No. E-013-1993/0-US-01).
Availability: Available for non-exclusive licensing.
Licensing Contact: Norbert Pontzer, Ph.D., J.D.; 301/435-5502;
pontzern@mail.nih.gov.
Dated: November 8, 2006.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. E6-19408 Filed 11-15-06; 8:45 am]
BILLING CODE 4140-01-P
