Government-Owned Inventions; Availability for Licensing, 29769-29770 [05-10316]
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Federal Register / Vol. 70, No. 99 / Tuesday, May 24, 2005 / Notices
awareness, concern, and knowledge
related to food safety.
FDA agrees that the data from the
food safety survey should be distributed
publicly through peer review journal
articles and though government
publications. It is anticipated that for
the first 6 months after collection, the
data will be analyzed internally. After 6
29769
months a summary will be produced
and made available to the public. Peer
reviewed journal articles are planned
following the summary.
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
No. of
Respondents
Questionnaire
Pretest
Annual Frequency
per Response
Total Annual
Responses
Hours per
Response
27
1
10,000
1
4,000
0.30
1,200
200
Nonresponse
27
4,000
Survey
1
10,000
Screener
0.5
1
200
0.10
20
0.0167
Total
1 There
Total Hours
14
167
1,401
are no capital costs or operating and maintenance costs associated with this collection of information.
The burden estimate is based on
FDA’s experience with the 2001 survey.
Prior to the survey being fielded, a small
pretest of 27 individuals (each pretest
lasting half an hour) will be conducted.
FDA estimates that the survey will
require an average of 20 minutes per
respondent and that the variation in
burden across respondents will be
small, based on average interview times
for the 2001 survey. The proposed
number of respondents is 4,000, each of
whom will be asked to complete a onetime telephone interview that requires
no preparation time. Additionally, 200
initial nonrespondents will be asked to
participate in a short version of the
survey to conduct a nonresponse
analysis. The screener is estimated to
take 1 minute or less per response for
a total screener burden of 4,000
respondents plus 6,000 ineligibles
screened, taking an estimated 167 hours.
The total hours reporting burden to the
public is the sum of the pretest, the
screener, the completed surveys, and
the nonresponse surveys, resulting in an
estimated public reporting burden of
1,401 hours.
Dated: May 17, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–10289 Filed 5–23–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, DHHS.
AGENCY:
VerDate jul<14>2003
17:36 May 23, 2005
Jkt 205001
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.
Treatment of Human Viral Infections
(Resveratrol)
Drs. Steven Zeichner and Vyjayanthi
Krishnan (NCI).
U.S. Provisional Application No. 60/
588,013 filed 13 Jul 2004 (DHHS
Reference No. E–279–2004/0–US–01).
Licensing Contact: Sally Hu; 301/435–
5606; hus@mail.nih.gov.
This application describes the
methods for treating or preventing an
HIV infection by the administration of
an Egr 1 activator called Resveratrol (3,
5, 4″-trihydroxystilbene) and its
derivatives. It has been known that HIV,
once it infects a cell, integrates into the
cellular genome and can (1) rapidly
undergo lytic infection, or (2) lay
dormant for a period of time (latent
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
infection). The existence of latent
infected cells poses a great challenge to
HIV therapy because (1) there are no
good existing means that can separate
the latent infected cells from the
uninfected cells; (2) even when
antiretroviral drugs are able to
completely suppress detectable HIV
replication, these latent infected cells
will remain and HIV can subsequently
complete the viral replication cycle to
produce more virus. Since Resveratrol
and its derivatives can activate lytic
replication from latent infected cells via
its effects on Erk1/2 signaling,
Resveratrol and its derivatives may lead
to therapies in which Resveratrol and/
or its derivatives is given together with
highly active antiretroviral therapy in an
effort to decrease or eliminate the
reservoir of latent infected cells with
hope of perhaps eventually curing a
patient of HIV infection.
Treatment of Human Viral Infections
(Proteosome Inhibitors)
Drs. Steven Zeichner and Vyjayanthi
Krishnan (NCI).
U.S. Provisional Application No. 60/
587,810 filed 13 Jul 2004 (DHHS
Reference No. E–280–2004/0–US–01).
Licensing Contact: Sally Hu; 301/435–
5606; hus@mail.nih.gov.
This application describes the
methods for treating or preventing an
HIV infection by the administration of
proteosome inhibitors and their
derivatives. It has been known that HIV,
once it infects a cell, integrates into the
cellular genome and can (1) rapidly
undergo lytic infection, or (2) lay
dormant for a period of time (latent
infection). The existence of latent
infected cells poses a great challenge to
HIV therapy because (1) there are no
good existing means that can separate
E:\FR\FM\24MYN1.SGM
24MYN1
29770
Federal Register / Vol. 70, No. 99 / Tuesday, May 24, 2005 / Notices
the latent infected cells from the
uninfected cells; (2) even when
antiretroviral drugs are able to
completely suppress detectable HIV
replication, these latent infected cells
will remain and HIV can subsequently
complete the viral replication cycle to
produce more virus. Since proteosome
inhibitors can activate lytic replication
from latent infected cells, proteosome
inhibitors may lead to therapies in
which proteosome inhibitors are given
together with highly active antiretroviral
therapy in an effort to decrease or
eliminate the reservoir of latent infected
cells with hope of perhaps eventually
curing a patient of HIV infection.
Treatment of Human Viral Infections
(Imatinib)
Drs. Steven Zeichner and Vyjayanthi
Krishnan (NCI).
U.S. Provisional Application No. 60/
588,015 filed 13 Jul 2004 (DHHS
Reference No. E–281–2004/0–US–01).
Licensing Contact: Sally Hu; 301/435–
5606; hus@mail.nih.gov.
This application describes the
methods for treating or preventing a HIV
infection by the administration of ablkinase inhibitor called imatinib and its
derivatives. Several available agents can
inhibit HIV replication by targeting one
or another viral protein, such as the
viral reverse transcriptase, protease,
envelope fusion process, or integrase, or
by targeting the interaction of a viral
component with a host cell component,
for example the host cell viral receptor
or co-receptor. However, HIV can
readily become resistant to these drugs,
and new therapeutic approaches for HIV
infection are needed. The studies
described in the application show that
the expression of many host cell genes
changes in response to HIV replication,
and show that targeting one of these
changes with imatinib can inhibit viral
replication. Thus targeting the host cell,
and making the host cell less hospitable
to the virus can inhibit viral replication.
The application thus describes a new
agent that inhibits viral replication by
acting on the host cell, which may offer
new approaches to therapy for HIV
infection. These approaches may be less
likely to engender rapid resistance in
the virus to the therapy.
Treatment of Human Viral Infections
(Farnesyl Transferase Inhibitors)
Drs. Steven Zeichner and Vyjayanthi
Krishnan (NCI).
U.S. Provisional Application No. 60/
587,771 filed 13 Jul 2004 (DHHS
Reference No. E–282–2004/0–US–01).
Licensing Contact: Sally Hu; 301/435–
5606; hus@mail.nih.gov.
VerDate jul<14>2003
17:36 May 23, 2005
Jkt 205001
This application describes the
methods for treating or preventing an
HIV infection by the administration of
farnesyl transferase inhibitors such as
FTI277, L–744832, BMS214662,
R115777 and SCH66336. It has been
known that HIV, once it infects a cell,
integrates into the cellular genome and
can (1) rapidly undergo lytic infection,
or (2) lay dormant for a period of time
(latent infection). The existence of latent
infected cells poses a great challenge to
HIV therapy because (1) there are no
good existing means that can separate
the latent infected cells from the
uninfected cells; (2) even when
antiretroviral drugs are able to
completely suppress detectable HIV
replication, these latent infected cells
will remain and HIV can subsequently
complete the viral replication cycle to
produce more virus. Since farnesyl
transferase inhibitors can activate lytic
replication from latent infected cells by
modulating membrane-bound Ras-Rho
levels, farnesyl transferase inhibitors
may lead to therapies in which farnesyl
transferase inhibitor is given together
with highly active antiretroviral therapy
in an effort to decrease or eliminate the
reservoir of latent infected cells with
hope of perhaps eventually curing a
patient of HIV infection.
Dated: May 17, 2005.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 05–10316 Filed 5–23–05; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
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
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.
Frm 00056
Fmt 4703
Dated: May 16, 2005.
LaVerne Y. Stringfield,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–10327 Filed 5–23–05; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Dental and
Craniofacial Research; Notice of
Meeting
BILLING CODE 4140–01–P
PO 00000
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel
Review of Research Projects (Cooperative
Agreements) U01s.
Date: May 27, 2005.
Time: 9 a.m. to 11 a.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Valerie L. Prenger, PhD,
Health Scientist Administrator, Review
Branch, Room 7214, Division of Extramural
Affairs, National Heart, Lung, and Blood
Institute, 6701 Rockledge Drive, MSC 7924,
Bethesda, MD 20892–7924, (301) 435–0270,
prengerv@nhlbi.nih.gov.
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.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Sfmt 4703
Notice is hereby given of a Conference
on Research Training Initiatives,
sponsored by the National Institute of
Dental and Craniofacial Research
(NIDCR).
The conference will be open to the
public as indicated below, with
attendance limited to space available.
This meeting will also be made
available by video cast at
https://videocast.nih.gov/.
Conference Name: Research Training
Initiatives.
Date: June 9, 2005.
Open: 8:30 a.m. to 5 p.m.
Agenda: The conference will focus on
a variety of issues relating to research
training. A significant portion of the
meeting will be devoted to discussion of
training of both clinician scientists and
basic scientists, from building a
pipeline, through undergraduate,
graduate and postgraduate research
training culminating in bridging to
scientific independence.
E:\FR\FM\24MYN1.SGM
24MYN1
]]>Agencies
[Federal Register Volume 70, Number 99 (Tuesday, May 24, 2005)]
[Notices]
[Pages 29769-29770]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10316]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, DHHS.
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.
Treatment of Human Viral Infections (Resveratrol)
Drs. Steven Zeichner and Vyjayanthi Krishnan (NCI).
U.S. Provisional Application No. 60/588,013 filed 13 Jul 2004 (DHHS
Reference No. E-279-2004/0-US-01).
Licensing Contact: Sally Hu; 301/435-5606; hus@mail.nih.gov.
This application describes the methods for treating or preventing
an HIV infection by the administration of an Egr 1 activator called
Resveratrol (3, 5, 4''-trihydroxystilbene) and its derivatives. It has
been known that HIV, once it infects a cell, integrates into the
cellular genome and can (1) rapidly undergo lytic infection, or (2) lay
dormant for a period of time (latent infection). The existence of
latent infected cells poses a great challenge to HIV therapy because
(1) there are no good existing means that can separate the latent
infected cells from the uninfected cells; (2) even when antiretroviral
drugs are able to completely suppress detectable HIV replication, these
latent infected cells will remain and HIV can subsequently complete the
viral replication cycle to produce more virus. Since Resveratrol and
its derivatives can activate lytic replication from latent infected
cells via its effects on Erk1/2 signaling, Resveratrol and its
derivatives may lead to therapies in which Resveratrol and/or its
derivatives is given together with highly active antiretroviral therapy
in an effort to decrease or eliminate the reservoir of latent infected
cells with hope of perhaps eventually curing a patient of HIV
infection.
Treatment of Human Viral Infections (Proteosome Inhibitors)
Drs. Steven Zeichner and Vyjayanthi Krishnan (NCI).
U.S. Provisional Application No. 60/587,810 filed 13 Jul 2004 (DHHS
Reference No. E-280-2004/0-US-01).
Licensing Contact: Sally Hu; 301/435-5606; hus@mail.nih.gov.
This application describes the methods for treating or preventing
an HIV infection by the administration of proteosome inhibitors and
their derivatives. It has been known that HIV, once it infects a cell,
integrates into the cellular genome and can (1) rapidly undergo lytic
infection, or (2) lay dormant for a period of time (latent infection).
The existence of latent infected cells poses a great challenge to HIV
therapy because (1) there are no good existing means that can separate
[[Page 29770]]
the latent infected cells from the uninfected cells; (2) even when
antiretroviral drugs are able to completely suppress detectable HIV
replication, these latent infected cells will remain and HIV can
subsequently complete the viral replication cycle to produce more
virus. Since proteosome inhibitors can activate lytic replication from
latent infected cells, proteosome inhibitors may lead to therapies in
which proteosome inhibitors are given together with highly active
antiretroviral therapy in an effort to decrease or eliminate the
reservoir of latent infected cells with hope of perhaps eventually
curing a patient of HIV infection.
Treatment of Human Viral Infections (Imatinib)
Drs. Steven Zeichner and Vyjayanthi Krishnan (NCI).
U.S. Provisional Application No. 60/588,015 filed 13 Jul 2004 (DHHS
Reference No. E-281-2004/0-US-01).
Licensing Contact: Sally Hu; 301/435-5606; hus@mail.nih.gov.
This application describes the methods for treating or preventing a
HIV infection by the administration of abl-kinase inhibitor called
imatinib and its derivatives. Several available agents can inhibit HIV
replication by targeting one or another viral protein, such as the
viral reverse transcriptase, protease, envelope fusion process, or
integrase, or by targeting the interaction of a viral component with a
host cell component, for example the host cell viral receptor or co-
receptor. However, HIV can readily become resistant to these drugs, and
new therapeutic approaches for HIV infection are needed. The studies
described in the application show that the expression of many host cell
genes changes in response to HIV replication, and show that targeting
one of these changes with imatinib can inhibit viral replication. Thus
targeting the host cell, and making the host cell less hospitable to
the virus can inhibit viral replication. The application thus describes
a new agent that inhibits viral replication by acting on the host cell,
which may offer new approaches to therapy for HIV infection. These
approaches may be less likely to engender rapid resistance in the virus
to the therapy.
Treatment of Human Viral Infections (Farnesyl Transferase Inhibitors)
Drs. Steven Zeichner and Vyjayanthi Krishnan (NCI).
U.S. Provisional Application No. 60/587,771 filed 13 Jul 2004 (DHHS
Reference No. E-282-2004/0-US-01).
Licensing Contact: Sally Hu; 301/435-5606; hus@mail.nih.gov.
This application describes the methods for treating or preventing
an HIV infection by the administration of farnesyl transferase
inhibitors such as FTI277, L-744832, BMS214662, R115777 and SCH66336.
It has been known that HIV, once it infects a cell, integrates into the
cellular genome and can (1) rapidly undergo lytic infection, or (2) lay
dormant for a period of time (latent infection). The existence of
latent infected cells poses a great challenge to HIV therapy because
(1) there are no good existing means that can separate the latent
infected cells from the uninfected cells; (2) even when antiretroviral
drugs are able to completely suppress detectable HIV replication, these
latent infected cells will remain and HIV can subsequently complete the
viral replication cycle to produce more virus. Since farnesyl
transferase inhibitors can activate lytic replication from latent
infected cells by modulating membrane-bound Ras-Rho levels, farnesyl
transferase inhibitors may lead to therapies in which farnesyl
transferase inhibitor is given together with highly active
antiretroviral therapy in an effort to decrease or eliminate the
reservoir of latent infected cells with hope of perhaps eventually
curing a patient of HIV infection.
Dated: May 17, 2005.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 05-10316 Filed 5-23-05; 8:45 am]
BILLING CODE 4140-01-P
