Public Workshop on Medical Devices and Nanotechnology: Manufacturing, Characterization, and Biocompatibility Considerations; Correction, 53704 [2010-21801]
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53704
Federal Register / Vol. 75, No. 169 / Wednesday, September 1, 2010 / Notices
Name of Committee: Center for Inherited
Disease Research Access Committee.
Date: September 14, 2010.
Time: 11:30 a.m. to 12:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 5635
Fishers Lane, Suite 4069, Bethesda, MD
20892, (Telephone Conference Call)
Contact Person: Ken D. Nakamura, PhD,
Scientific Review Officer, Scientific Review
Branch, National Human Genome Research
Institute, National Institutes of Health, 5635
Fishers Lane, Suite 4076, MSC 9306,
Rockville, MD 20852, 301–402–0838.
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. 93.172, Human Genome
Research, National Institutes of Health, HHS)
Dated: August 26, 2010.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–21819 Filed 8–31–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive
License: Use of Pentosan Polysulfate
To Treat Certain Conditions of the
Prostate
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
AGENCY:
This is notice, in accordance
with 35 U.S.C. 209(c)(1) and 37 CFR
404.7(a)(1)(i), that the National
Institutes of Health (NIH), Department
of Health and Human Services, is
contemplating the grant of an exclusive
patent license to practice the invention
embodied in U.S. Patent Application
No. 10/209,331, filed July 30, 2002,
which was issued as U.S. Patent
6,828,309 on December 07, 2004,
entitled, ‘‘USE OF PENTOSAN
POLYSULFATE TO TREAT CERTAIN
CONDITIONS OF THE PROSTATE,’’
developed by Dr. Gary Striker (formerly
of NIDDK) [HHS Ref. No. E–104–1997/
0–US–03], to Swati Spentose Private
Limited, having a place of business in
Mumbai, India. The patent rights in this
invention have been assigned to the
United States of America.
The contemplated exclusive license
territory may be worldwide, and the
field of use may be limited to ‘‘the use
of pentosan polysulfate for the treatment
or prevention of benign prostatic
hyperplasia.’’
hsrobinson on DSK69SOYB1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
18:24 Aug 31, 2010
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Only written comments and/or
application for a license which are
received by the NIH Office of
Technology Transfer on or before
October 1, 2010 will be considered.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Requests for copies of the
patents, inquiries, comments, and other
materials relating to the contemplated
license should be directed to:
Suryanarayana Vepa, PhD, J.D.,
Licensing and Patenting Manager, Office
of Technology Transfer, National
Institutes of Health, 6011 Executive
Boulevard, Suite 325, Rockville, MD
20852–3804; Telephone: 301–435–5020;
Facsimile: 301–402–0220; E-mail:
vepas@mail.nih.gov.
[Docket No. FDA–2010–N–0427]
DATES:
ADDRESSES:
This
technology is a method for treating
Benign Prostatic Hyperplasia (BHP)
using the oral medication pentosan
polysulfate (PPS). PPS is a well known,
semi-synthetic polysaccharide extracted
from beech wood cellulose that is FDA
approved for the treatment of interstitial
fibrosis. The current technology builds
on the surprising discovery that PPS can
cause regression of scarring and lesions
in prostatic tissue. PPS reduces or
eliminates both smooth muscle cell
proliferation and extracellular matrix
deposition, and so reduces the size of
the prostate gland and decreases
associated obstructive symptoms.
The prospective exclusive license will
be royalty-bearing and will comply with
the terms and conditions of 35 U.S.C.
209 and 37 CFR 404.7. The prospective
exclusive license may be granted unless,
within 30 days from the date of this
published Notice, the NIH receives
written evidence and argument that
establishes that the grant of the license
would not be consistent with the
requirements of 35 U.S.C. 209 and 37
CFR 404.7.
Applications for a license in the
prospective field of use filed in response
to this notice will be treated as
objections to the grant of the
contemplated exclusive license.
Comments and objections submitted in
response to this notice will not be made
available for public inspection, and, to
the extent permitted by law, will not be
released under the Freedom of
Information Act, 5 U.S.C. 552.
SUPPLEMENTARY INFORMATION:
Food and Drug Administration
Public Workshop on Medical Devices
and Nanotechnology: Manufacturing,
Characterization, and Biocompatibility
Considerations; Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; correction.
The Food and Drug
Administration (FDA) is correcting a
notice that appeared in the Federal
Register of August 23, 2010 (75 FR
51829). The notice announced the
public workshop entitled ‘‘Medical
Devices & Nanotechnology:
Manufacturing, Characterization, and
Biocompatibility Considerations.’’ The
notice was published with an incorrect
registration Web site. This document
corrects that Web site.
SUMMARY:
Paul
Gadiock, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, rm. 4432, Silver Spring,
MD 20993–0002, 301–796–5736.
FOR FURTHER INFORMATION CONTACT:
In FR Doc.
2010–20837, appearing on page 51829
in the Federal Register of Monday,
August 23, 2010, the following
correction is made:
1. On page 51829, in the second
column, in the Registration and
Requests for Oral Presentations section,
in the first full paragraph, beginning in
the third line, ‘‘https://www.fda.gov/
MedicalDevices/NewsEvents/
WorskshopsConferences/default.htm’’ is
corrected to read ‘‘https://www.fda.gov/
MedicalDevices/NewsEvents/
WorkshopsConferences/default.htm’’.
SUPPLEMENTARY INFORMATION:
Dated: August 27, 2010.
David Dorsey,
Acting Deputy Commissioner for Policy,
Planning and Budget.
[FR Doc. 2010–21801 Filed 8–31–10; 8:45 am]
BILLING CODE 4160–01–S
Dated: August 25, 2010.
Richard U. Rodriguez,
Director, Division of Technology Development
& Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 2010–21818 Filed 8–31–10; 8:45 am]
BILLING CODE 4140–01–P
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Agencies
[Federal Register Volume 75, Number 169 (Wednesday, September 1, 2010)]
[Notices]
[Page 53704]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-21801]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0427]
Public Workshop on Medical Devices and Nanotechnology:
Manufacturing, Characterization, and Biocompatibility Considerations;
Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is correcting a notice
that appeared in the Federal Register of August 23, 2010 (75 FR 51829).
The notice announced the public workshop entitled ``Medical Devices &
Nanotechnology: Manufacturing, Characterization, and Biocompatibility
Considerations.'' The notice was published with an incorrect
registration Web site. This document corrects that Web site.
FOR FURTHER INFORMATION CONTACT: Paul Gadiock, Food and Drug
Administration, 10903 New Hampshire Ave., Bldg. 66, rm. 4432, Silver
Spring, MD 20993-0002, 301-796-5736.
SUPPLEMENTARY INFORMATION: In FR Doc. 2010-20837, appearing on page
51829 in the Federal Register of Monday, August 23, 2010, the following
correction is made:
1. On page 51829, in the second column, in the Registration and
Requests for Oral Presentations section, in the first full paragraph,
beginning in the third line, ``https://www.fda.gov/MedicalDevices/NewsEvents/WorskshopsConferences/default.htm'' is corrected to read
``https://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/default.htm''.
Dated: August 27, 2010.
David Dorsey,
Acting Deputy Commissioner for Policy, Planning and Budget.
[FR Doc. 2010-21801 Filed 8-31-10; 8:45 am]
BILLING CODE 4160-01-S