National Institutes of Neurological Disorders and Stroke; Notice of Closed Meetings, 37030-37031 [07-3292]
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Federal Register / Vol. 72, No. 129 / Friday, July 6, 2007 / Notices
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Modification of Recombinant AntiTumor RNase (rapLR1) for Optimal Use
in the Large Scale Manufacture of
Stable and Potent RapLR1-Antibody
Conjugates
Description of Technology: This
technology involves modified rapLR1
molecules having an improved capacity
for conjugation to targeting moieties.
Previously, techniques for attaching
wild-type rapLR1 to a targeting moiety
required an excess of RNase, leading to
high production costs. The inventors
have now mutated specific amino acids
in rapLR1 to allow a more efficient (and
therefore less costly) conjugation
reaction.
Members of the ribonuclease A
(RNase A) superfamily, such as rapLR1,
have the ability to efficiently kill a wide
range of cancer cells. Ligand binding
moieties such as antibodies or peptides
can be used to target RNases to a
particular cell or cell type that expresses
a marker, e.g., a marker that is
associated with cancer. The current
invention provides rapLR1 molecules
that have been genetically modified to
contain a cysteine at a specific location
that does not interfere with the
enzymatic activity of the molecule. The
inserted cysteine provides the advantage
of a site-directed and specific
attachment of rapLR1 to targeting
moieties, which results in more efficient
production of the therapeutic. This
significantly reduces the cost of bringing
rapLR1-related cancer therapeutics to
market.
Applications: Targeted anti-cancer
therapy molecules; Targeting moiety can
be interchanged based on target cancer
cells; Targeting any disease in which the
cell is transformed and presents unique
levels of cell surface markers.
Advantages: RapLR1 delivery,
specificity and toxicity to cancer cells is
increased by conjugation to a targeting
moiety; Modified rapLR1 increases
conjugation efficiency, making the
preparation of the anti-cancer agents
more cost effective without sacrificing
specificity.
Benefits: Cancer is the second leading
cause of death in the United States, with
approximately 600,000 cancer-related
deaths occurring in 2006 alone. Because
rapLR1 can be used to treat a number of
different cancers (depending on the
targeting moiety), there is a powerful
social benefit from this technology:
Improving the duration and quality of
life of a wide range of cancer patients.
Furthermore, the cancer therapeutic
market is expected to reach $27 billion
by 2009. Because rapLR1 can now be
efficiently conjugated to targeting
moieties, there is an opportunity to
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occupy a significant niche in that
predicted market, with lower cost to the
licensee.
Inventors: Dianne L. Newton et al.
(NCI).
U.S. Patent Status: Pending PCT
Application PCT/US2006/038180,
published as WO 2007/041361 (HHS
Reference No. E–265–2005/0–PCT–02).
Licensing Contact: David A.
Lambertson, PhD; Phone: (301) 435–
4632; Fax: (301) 402–0220; E-mail:
lambertsond@mail.nih.gov.
Methods for Expression and
Purification of Immunotoxins
Description of Technology: The
invention concerns immunotoxins and
methods of making the immunotoxins.
Targeting of the immunotoxins occurs
via an antibody that is specific to T
cells. This allows the specific ablation
of malignant T cells and resting T cells.
The transient ablation of resting T cells
can ‘‘reset’’ the immune system by
accentuating tolerizing responses. As a
result, the immunotoxin can be used to
treat autoimmune disease, malignant T
cell-related cancers, and graft-versushost disease. The toxin portion of the
immunotoxin is engineered to maintain
bioactivity when produced in yeast,
specifically Pichia pastoris. This system
allows the production of dimeric
antibody fragments with increased
binding affinity and potency.
Applications: Immunotoxins
produced by this method can be used
for the treatment of autoimmune
diseases such as multiple sclerosis,
lupus, type I diabetes, aplastic anemia;
Immunotoxins produced by this method
can be used for treatment of T-cell
leukemias and lymphomas such as
cutaneous T cell leukemia/lymphoma
(CTCL); Immunotoxins produced by this
method can be used for increasing
immune tolerance in patients requiring
transplants/grafts.
Advantages: Method produces GMP
quality immunotoxin and can be scaled
up to industry scales; Modified toxin
moiety has reduced glycosylation in this
system, resulting in a more effective and
efficient immunotoxin; Immunotoxin
doesn’t produce the deleterious sideeffects seen with other methods of
treating autoimmune disease, malignant
T cell leukemia/lymphoma and graftversus-host disease.
Benefits: New methods and
compositions with limited side-effects
have the potential to revolutionize
treatment of autoimmune disease;
provides an opportunity to capture a
significant market share for the millions
of people who suffer from an
autoimmune disease.
Inventors: David Neville et al. (NIMH)
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Patent Status: U.S. Patent Application
No. 10/566,886 filed 01 Feb 2006, which
published as U.S. 2006/0216782 on 28
Sep 2006 (HHS Reference No. E–043–
1997/2–US–03); U.S. Patent No.
6,632,928 issued 14 Oct 2003 (HHS
Reference No. E–044–1997/0–US–07);
U.S. Patent Application No. 10/435,567
filed 09 May 2003, which published as
2003/0185825 on 02 Oct 2003 (HHS
Reference No. E–044–1997/0–US–08);
U.S. Patent Application No. 10/296,085
filed 18 Nov 2002, which published as
2004/0127682 on 01 Jul 2004 (HHS
Reference No. E–044–1997/1–US–06);
Foreign rights are also available.
Licensing Status: Available for
exclusive or non-exclusive licensing.
Licensing Contact: David A.
Lambertson, PhD; 301/435–4632;
lambertsond@mail.nih.gov.
Collaborative Research Opportunity:
The National Institute of Mental Health,
Laboratory of Molecular Biology, is
seeking statements of capability or
interest from parties interested in
collaborative research to further
develop, evaluate, or commercialize
methods of expression and purification
of immunotoxins. Please contact David
Neville at davidn@mail.nih.gov for more
information.
Dated: June 28, 2007.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E7–13128 Filed 7–5–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institutes of Neurological
Disorders and Stroke; Notice of Closed
Meetings
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
meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in section 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.
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Federal Register / Vol. 72, No. 129 / Friday, July 6, 2007 / Notices
Name of Committee: National Institutes of
Neurological Disorders and Stroke Special
Emphasis Panel, Texas–SNRP.
Date: July 16–17, 2007.
Time: 8 a.m. to 1 p.m.
Agenda: To review and evaluate grant
applications.
Place: Marriott San Antonio Riverwalk,
711 East River Walk, San Antonio, TX 78205.
Contact Person: Philip F. Wiethorn,
Scientific Review Administrator, DHHS/NIH/
NINDS/DER/SRB, 6001 Executive Boulevard;
MSC 9529, Neuroscience Center; Room 3203,
Bethesda, MD 20892–9529, (301) 496–5388,
wiethorp@ninds.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.
Name of Committee: National Institutes of
Neurological Disorders and Stroke Special
Emphasis Panel, Neurofibromatosis/
Tuberous Sclerosis.
Date: July 24, 2007.
Time: 11 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Telephone
Conference Call).
Contact Person: Shantadurga Rajaram,
PHD, Scientific Review Administrator,
Scientific Review Branch, NIH/NINDS/
Neuroscience Center, 6001 Executive Blvd.,
Suite 3208, Msc 9529, Bethesda, MD 20852,
(301) 435–6033, rajarams@mail.nih.gov.
The 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. 93.853, Clinical Research
Related to Neurological Disorders; 93.854,
Biological Basis Research in the
Neurocsciences, National Institutes of Health,
HHS)
Dated: June 29, 2007.
Anna Snouffer,
Acting Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 07–3292 Filed 7–5–07; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
mstockstill on PROD1PC66 with NOTICES
National Institute of Child Health and
Human Development; 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.,
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as amended. The contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development
Special Emphasis Panel, International and
Domestic Pediatric and Maternal HIV Studies
Coordinating Center.
Date: July 31, 2007.
Time: 11:55 a.m. to 1:30 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institutes of Health, 6100
Executive Boulevard, Rockville, MD 20852
(Telephone Conference Call).
Contact Person: Hameed Khan, PhD,
Scientific Review Administrator, Division of
Scientific Review, National Institute of Child
Health and Human Development, NIH, 6100
Executive Blvd., Room 5B01 Bethesda, MD
20892, (301) 435–6902, khanh@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment Program, National
Institutes of Health, HHS)
Dated: June 29, 2007.
Anna Snouffer,
Acting Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 07–3294 Filed 7–5–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Drug Abuse;
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.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel, Imaging
of Drug Use Prevention Messages (R21).
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37031
Date: July 24, 2007.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: The Fairmont Washington, DC, 2401
M Street, NW, Washington, DC 20037.
Contact Person: Mark R. Green, PhD,
Deputy Director, Office of Extramural Affairs,
National Institute on Drug Abuse, NIH,
DHHS, Room 220, MSC 8401, 6101 Executive
Boulevard, Bethesda, Md 20892–8401, (301)
435–1431, mgreen1@nida.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. 93.279, Drug Abuse and
Addiction Research Programs. National
Institutes of Health, HHS)
Dated: June 29, 2007.
Anna Snoufer,
Acting Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 07–3295 Filed 7–05–07; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of
Closed Meetings
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
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: National Institute on
Aging Special Emphasis Panel, Cognition and
Hippocampal Aging.
Date: July 17, 2007.
Time: 1 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, 7201 Wisconsin Avenue,
2C212, Bethesda, MD 20814 (Telephone
Conference Call).
Contact Person: William Cruce, PhD,
Health Scientist Administrator, Scientific
Review Office, National Institute on Aging,
National Institutes of Health, Room 2C212,
7201 Wisconsin Avenue, Bethesda, MD
20814, 301–402–7704, crucew@nia.nih.gov.
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Agencies
[Federal Register Volume 72, Number 129 (Friday, July 6, 2007)]
[Notices]
[Pages 37030-37031]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-3292]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Institutes of Neurological Disorders and Stroke; Notice
of Closed Meetings
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
meetings.
The meetings will be closed to the public in accordance with the
provisions set forth in section 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.
[[Page 37031]]
Name of Committee: National Institutes of Neurological Disorders
and Stroke Special Emphasis Panel, Texas-SNRP.
Date: July 16-17, 2007.
Time: 8 a.m. to 1 p.m.
Agenda: To review and evaluate grant applications.
Place: Marriott San Antonio Riverwalk, 711 East River Walk, San
Antonio, TX 78205.
Contact Person: Philip F. Wiethorn, Scientific Review
Administrator, DHHS/NIH/NINDS/DER/SRB, 6001 Executive Boulevard; MSC
9529, Neuroscience Center; Room 3203, Bethesda, MD 20892-9529, (301)
496-5388, wiethorp@ninds.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.
Name of Committee: National Institutes of Neurological Disorders
and Stroke Special Emphasis Panel, Neurofibromatosis/Tuberous
Sclerosis.
Date: July 24, 2007.
Time: 11 a.m. to 5 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institutes of Health, Neuroscience Center, 6001
Executive Boulevard, Rockville, MD 20852 (Telephone Conference
Call).
Contact Person: Shantadurga Rajaram, PHD, Scientific Review
Administrator, Scientific Review Branch, NIH/NINDS/Neuroscience
Center, 6001 Executive Blvd., Suite 3208, Msc 9529, Bethesda, MD
20852, (301) 435-6033, rajarams@mail.nih.gov.
The 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. 93.853,
Clinical Research Related to Neurological Disorders; 93.854,
Biological Basis Research in the Neurocsciences, National Institutes
of Health, HHS)
Dated: June 29, 2007.
Anna Snouffer,
Acting Director, Office of Federal Advisory Committee Policy.
[FR Doc. 07-3292 Filed 7-5-07; 8:45 am]
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