Prospective Grant of Exclusive License: Treatment of Acute and Chronic Neurological Injuries Involving Axonal Regeneration, 38714 [2015-16500]
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Federal Register / Vol. 80, No. 129 / Tuesday, July 7, 2015 / Notices
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Dated: June 30, 2015.
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[FR Doc. 2015–16503 Filed 7–6–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
tkelley on DSK3SPTVN1PROD with NOTICES
National Institutes of Health
Prospective Grant of Exclusive
License: Treatment of Acute and
Chronic Neurological Injuries Involving
Axonal Regeneration
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
VerDate Sep<11>2014
20:31 Jul 06, 2015
Jkt 235001
This is notice, in accordance
with 35 U.S.C. 209 and 37 CFR part 404,
that the National Institutes of Health,
Department of Health and Human
Services, is contemplating the grant of
an exclusive patent license to practice
the following inventions embodied in
the following patent applications:
SUMMARY:
HHS Ref. No.: E–214–2012/0
Titled: ‘‘Compositions and Methods for the
Treatment of Central Nervous System
Injury’’
1. US Provisional Patent Application No.:
61/705,555 HHS Ref. No.: E–214–2012/
0–US–01 Filing Date: September 25,
2012
2. PCT Patent Application No.: PCT/
US2013/061693 HHS Ref. No.: E–214–
2012/0–PCT–02 Filing Date: September
25, 2013
3. Australian Patent Application No.:
2013–32367 HHS Ref No.: E–214–2012/
0–AU–03 Filing Date: September 25,
2013
4. European Patent Application No.:
13771750 HHS Ref. No.: E–214–2012/0–
EP–04 Filing Date: September 25, 2013
5. U.S. Patent Application No.: 14/430,850
HHS Ref. No.: E–214–2012/0–US–06
Filing Date: September 25, 2013
to BioAxone Biosciences Incorporated
(‘‘BioAxone’’), a company incorporated
under the laws of the State of Delaware
having an office in at least Cambridge,
Massachusetts, U.S.A. The patent rights
in these inventions have been assigned
to the United States of America.
BioAxone is seeking all worldwide
territories for this license. The field of
use may be limited to ‘‘Treatment of
human acute and chronic neurological
injuries involving axonal regeneration,
as monotherapy or in combination with
other therapeutic drugs or medical
devices’’.
Only written comments and/or
applications for a license which are
received by the NIH Office of
Technology Transfer on or before
August 6, 2015 will be considered.
ADDRESSES: Requests for copies of the
patent application, patents, inquiries,
comments, and other materials relating
to the contemplated exclusive license
should be directed to: Cristina
Thalhammer-Reyero, Ph.D., M.B.A.,
Office of Technology Transfer, National
Institutes of Health, 6011 Executive
Boulevard, Suite 325, Rockville, MD
20852–3804; Telephone: (301) 435–
4507; Facsimile: (301) 402–0220; Email:
thalhamc@mail.nih.gov. A signed
confidentiality nondisclosure agreement
will be required to receive copies of any
patent applications or patents that have
not been published or issued by the
United States Patent and Trademark
Office or the World Intellectual Property
Organization.
DATES:
PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
This
technology, and its corresponding
patent applications, is directed to
methods of treating or preventing spinal
cord injury or a glial scar by
administering an agent that reduces the
amount or activity of a 4-sulfacted
GalNAc in a chondroitin
glycosaminoglycan chain, wherein said
agent includes human enzyme,
arylsulfatase B (ARSB). This technology,
and its corresponding patent
applications, is also directed to methods
of increasing neuron growth,
proliferation, or migration by
administering an agent that reduces the
amount or activity of a 4-sulfacted
GalNAc in a chondroitin
glycosaminoglycan chain, wherein said
agent includes ARSB. This technology
may be useful as a means to treat
paralysis and motor defects induced by
spinal cord injury, such as by promoting
axonal regrowth.
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 part 404. The
prospective exclusive license may be
granted unless within thirty (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 part 404.
Properly filed competing applications
for a license in response to this notice
will be treated as objections to the
contemplated 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:
Dated: June 30, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology
Transfer, National Institutes of Health.
[FR Doc. 2015–16500 Filed 7–6–15; 8:45 am]
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Reduction Act of 1995, the National
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SUMMARY:
E:\FR\FM\07JYN1.SGM
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[Federal Register Volume 80, Number 129 (Tuesday, July 7, 2015)]
[Notices]
[Page 38714]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-16500]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive License: Treatment of Acute and
Chronic Neurological Injuries Involving Axonal Regeneration
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This is notice, in accordance with 35 U.S.C. 209 and 37 CFR
part 404, that the National Institutes of Health, Department of Health
and Human Services, is contemplating the grant of an exclusive patent
license to practice the following inventions embodied in the following
patent applications:
HHS Ref. No.: E-214-2012/0
Titled: ``Compositions and Methods for the Treatment of Central
Nervous System Injury''
1. US Provisional Patent Application No.: 61/705,555 HHS Ref.
No.: E-214-2012/0-US-01 Filing Date: September 25, 2012
2. PCT Patent Application No.: PCT/US2013/061693 HHS Ref. No.:
E-214-2012/0-PCT-02 Filing Date: September 25, 2013
3. Australian Patent Application No.: 2013-32367 HHS Ref No.: E-
214-2012/0-AU-03 Filing Date: September 25, 2013
4. European Patent Application No.: 13771750 HHS Ref. No.: E-
214-2012/0-EP-04 Filing Date: September 25, 2013
5. U.S. Patent Application No.: 14/430,850 HHS Ref. No.: E-214-
2012/0-US-06 Filing Date: September 25, 2013
to BioAxone Biosciences Incorporated (``BioAxone''), a company
incorporated under the laws of the State of Delaware having an office
in at least Cambridge, Massachusetts, U.S.A. The patent rights in these
inventions have been assigned to the United States of America. BioAxone
is seeking all worldwide territories for this license. The field of use
may be limited to ``Treatment of human acute and chronic neurological
injuries involving axonal regeneration, as monotherapy or in
combination with other therapeutic drugs or medical devices''.
DATES: Only written comments and/or applications for a license which
are received by the NIH Office of Technology Transfer on or before
August 6, 2015 will be considered.
ADDRESSES: Requests for copies of the patent application, patents,
inquiries, comments, and other materials relating to the contemplated
exclusive license should be directed to: Cristina Thalhammer-Reyero,
Ph.D., M.B.A., Office of Technology Transfer, National Institutes of
Health, 6011 Executive Boulevard, Suite 325, Rockville, MD 20852-3804;
Telephone: (301) 435-4507; Facsimile: (301) 402-0220; Email:
thalhamc@mail.nih.gov. A signed confidentiality nondisclosure agreement
will be required to receive copies of any patent applications or
patents that have not been published or issued by the United States
Patent and Trademark Office or the World Intellectual Property
Organization.
SUPPLEMENTARY INFORMATION: This technology, and its corresponding
patent applications, is directed to methods of treating or preventing
spinal cord injury or a glial scar by administering an agent that
reduces the amount or activity of a 4-sulfacted GalNAc in a chondroitin
glycosaminoglycan chain, wherein said agent includes human enzyme,
arylsulfatase B (ARSB). This technology, and its corresponding patent
applications, is also directed to methods of increasing neuron growth,
proliferation, or migration by administering an agent that reduces the
amount or activity of a 4-sulfacted GalNAc in a chondroitin
glycosaminoglycan chain, wherein said agent includes ARSB. This
technology may be useful as a means to treat paralysis and motor
defects induced by spinal cord injury, such as by promoting axonal
regrowth.
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 part
404. The prospective exclusive license may be granted unless within
thirty (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 part 404.
Properly filed competing applications for a license in response to
this notice will be treated as objections to the contemplated 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.
Dated: June 30, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology Transfer, National Institutes of
Health.
[FR Doc. 2015-16500 Filed 7-6-15; 8:45 am]
BILLING CODE 4140-01-P