Prospective Modification of Exclusive Patent License Potent and Selective Analogues of: Monamine Transporters; Methods of Making; and Uses Thereof, 45865-45866 [2017-21048]
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Federal Register / Vol. 82, No. 189 / Monday, October 2, 2017 / Notices
sradovich on DSK3GMQ082PROD with NOTICES
the corresponding reference listed drugs
or reference standards:
a. How to effectively integrate systems
pharmacology, PBPK, and the exposureclinical response relationship to
evaluate product risk and assist BE
evaluation?
b. What will be the next generation
methodologies in postmarket signal
detection to evaluate product
substitution or compare product
performance using the Sentinel database
or complementary toolsets?
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midnight, Eastern Standard Time. Early
registration is recommended because
seating is limited; therefore, FDA may
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due to a disability, please contact
Lanyan (Lucy) Fang (see FOR FURTHER
INFORMATION CONTACT) no later than 7
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VerDate Sep<11>2014
19:01 Sep 29, 2017
Jkt 244001
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ADDRESSES). A link to the transcript will
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ucm554182.htm.
Dated: September 26, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning,
Legislation, and Analysis.
[FR Doc. 2017–21017 Filed 9–29–17; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Modification of Exclusive
Patent License Potent and Selective
Analogues of: Monamine Transporters;
Methods of Making; and Uses Thereof
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
The National Institute of Drug
Abuse, an institute of the National
Institutes of Health, Department of
Health and Human Services is
contemplating the modification of grant
of an Exclusive Patent License to
EncepHeal Therapeutics, Inc., located in
Winston-Salem, North Carolina, to
practice the inventions embodied in the
patent applications listed in the
Supplementary Information section of
this notice.
DATES: Only written comments and/or
applications for a license which are
received by the National Institute on
Drug Abuse’s Technology Transfer
Office on or before October 17, 2017
will be considered.
SUMMARY:
PO 00000
Frm 00071
Fmt 4703
Sfmt 4703
45865
Requests for copies of the
patent application, inquiries, and
comments relating to the contemplated
modification of the Exclusive Patent
License should be directed to Martha
Lubet, Ph.D., Technology Transfer
Manager, NCI TTC, 9609 Medical Center
Drive, Room IE350, MSC 9702,
Rockville, MD 20850. Telephone: 240
276–5508. Facsimile: 240 276–5505.
Email: lubetm@mail.nih.gov.
SUPPLEMENTARY INFORMATION: The
following represents the intellectual
property to be licensed under the
prospective agreement:
U.S. provisional application 61/
774,878, filed March 8, 2013 entitled
‘‘Potent and Selective Inhibitors of
Monamine Transporters; Methods of
Making; and Uses Thereof’’ [HHS Ref.
No. E–073–2013/0–US–01];
PCT application PCT/US2014/021514,
filed March 7, 2014 entitled ‘‘Potent and
Selective Analogues of: Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–PCT–02];
U.S. application 14/772,486, filed
September 3, 2015 entitled ‘‘Potent and
Selective Analogues of Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–US–06];
EPO application 14714043.8, filed
September 1, 2015 entitled ‘‘Potent and
Selective Analogues of Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–EP–05];
Australian application 2014225550,
filed September 8, 2015 entitled ‘‘Potent
and Selective Analogues of Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–AU–03];
Australian application 2017202849,
filed April 28, 2017 entitled Potent and
Selective Analogues of Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–AU–07];
Canadian application 2903746, filed
September 2, 2015 entitled ‘‘Potent and
Selective Analogues of Monamine
Transporters; Methods of Making; and
Uses Thereof’’ [HHS Ref. No. E–073–
2013/0–CA–04];
The patent rights to these inventions
have been assigned to and/or
exclusively licensed to the Government
of the United States of America.
The Government previously
announced its intention to grant an
exclusive license to EncepHeal at FR
80:245 (December 22, 2015), pp. 79595–
79596.
The Notice of Intent to Grant (NOITG)
specified a Field of Use as ‘‘Use of
ADDRESSES:
E:\FR\FM\02OCN1.SGM
02OCN1
sradovich on DSK3GMQ082PROD with NOTICES
45866
Federal Register / Vol. 82, No. 189 / Monday, October 2, 2017 / Notices
analogues of monamine transporters to
treat substance use disorders and sleep
disorders within the scope of the
Licensed Patent Rights’’. Comments/
Objections were not received in
response to the NOITG. After
consideration, an exclusive license was
granted to EncepHeal with a Licensed
Field of Use of: ‘‘Use of analogues of
monamine transporters to treat
substance use disorders within the
scope of the Licensed Patent Rights’’.
This Notice advises the public that the
NIH intends to modify the Licensed
Field of Use originally granted to
EncepHeal. Specifically, the National
Institute on Drug Abuse is proposing to
modify the Licensed Field of Use to be
‘‘use of a lead compound to treat one or
more of the following: Substance use
disorders, cognitive deficits, sleep
disorders, attention deficit hyperactivity
disorder and depressive disorders. The
modification to the Licensed Field of
Use in the Exclusive Patent License
requires EncepHeal to select a lead
compound for each of the disorders
listed in the Field of Use and that upon
selection of a lead compound for a
disorder, the other compounds of the
technology will become available for
licensing to other companies.
The technology is directed to novel
analogues of modafinil. Modafinil
(marketed as Provisil in United States)
is approved by FDA to treat narcolepsy
and other sleep disorders. Modafinil has
been studied as a possible treatment for
cognitive dysfunction in disorders such
as attention-deficit hyperactivity
disorders (ADHD) as well as cocaine
and methamphetamine addiction.
However, it has a relatively low affinity
for dopamine transporter (DAT) and is
water-insoluble, thus requiring large
doses to achieve pharmacological
effects. Early studies indicated that
modafinil reduced cocaine intake more
effectively than placebo; however,
subsequent larger studies reported only
modest effectiveness in reducing
cocaine intake. The library of
compounds in the technology are
analogs of modafinil and are designed to
have higher affinities for DAT and
improved water solubility. The National
Institute on Drug Abuse has conducted
preliminary experiments on many of the
compounds and has identified several
compounds that have higher affinities
than modafinil for the DAT and lower
affinity than modafinil for several other
off target receptors. Preliminary studies
at the National Institute on Drug Abuse
indicate that some of the compounds
have in vivo activity in rodents to
inhibit cocaine taking behavior and are
not selectively self-administered
VerDate Sep<11>2014
19:01 Sep 29, 2017
Jkt 244001
themselves (i.e. have low abuse
liability).
This notice is made in accordance
with 35 U.S.C. 209 and 37 CFR part 404
and incorporates by reference:
‘‘Prospective Grant of Exclusive Option
License: Potent and Selective Analogues
of: Monamine Transporters; Methods of
Making; and Uses Thereof’’ FR 80:245
(December 22, 2015), pp. 79595–79596.
The prospective modification of the
Exclusive Patent License will be royalty
bearing and may be granted unless
within fifteen (15) days from date of this
published notice, the National Institute
on Drug Abuse receives written
evidence and argument that establishes
that the grant of modification to the
license would not be consistent with the
requirements of 35 U.S.C. 209 and 37
CFR Part 404.
Complete applications for a license in
the field of use filed in response to this
notice will be treated as objections to
the grant of the contemplated
modification to Exclusive Patent
License. Comments and objections
submitted 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: September 22, 2107.
Richard U. Rodriguez,
Associate Director, Technology Transfer
Center, National Cancer Institute.
[FR Doc. 2017–21048 Filed 9–29–17; 8:45 am]
BILLING CODE 4040–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Neurological
Disorders and Stroke; Notice of Closed
Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, 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 of
Neurological Disorders and Stroke Special
Emphasis Panel; Program Project Grant P01.
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
Date: October 23, 2017.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852
(Teleconference Meeting).
Contact Person: Ana Olariu, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, NINDS/NIH/DHHS, Neuroscience
Center, 6001 Executive Blvd., Suite 3204,
MSC 9529, Bethesda, MD 20892–9529, (301)
496–9223, ana.olariu@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Initial
Review Group; Neurological Sciences and
Disorders A.
Date: October 23–24, 2017.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Melrose Hotel, 2430 Pennsylvania
Avenue NW., Washington, DC 20037.
Contact Person: Natalia Strunnikova,
Ph.D., Scientific Review Officer, Scientific
Review Branch, NINDS/NIH/DHHS,
Neuroscience Center, 6001 Executive Blvd.,
Suite 3204, MSC 9529, Bethesda, MD 20892–
9529, (301) 402–0288, natalia.strunnikova@
nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; K99/R00 Review.
Date: October 23, 2017.
Time: 11:30 a.m. to 1:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Crystal City, 2399 Jefferson
Davis Highway, Arlington, VA 22202.
Contact Person: Elizabeth A. Webber,
Ph.D., Scientific Review Officer, Scientific
Review Branch, NINDS/NIH/DHHS,
Neuroscience Center, 6001 Executive Blvd.,
Suite 3204, MSC 9529, Bethesda, MD 20892–
9529, (301) 496–1917, webbere@mail.nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Initial
Review Group; Neurological Sciences and
Disorders B.
Date: October 26–27, 2017.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Admiral Fell Inn, 888 South
Broadway, Baltimore, MD 21231.
Contact Person: Birgit Neuhuber, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, NINDS/NIH/DHHS, Neuroscience
Center, 6001 Executive Blvd., Suite 3204,
MSC 9529, Bethesda, MD 20892–9529, (301)
496–9223, neuhuber@ninds.nih.gov@nih.gov.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; Ruth L. Kirschstein National
Research Service Award (NRSA) Institutional
Research Training Grant (T32) Program.
Date: October 30–31, 2017.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hotel Monaco, 700 F Street NW.,
Washington, DC 20001.
Contact Person: William Benzing, Ph.D.,
Scientific Review Officer, Scientific Review
E:\FR\FM\02OCN1.SGM
02OCN1
Agencies
[Federal Register Volume 82, Number 189 (Monday, October 2, 2017)]
[Notices]
[Pages 45865-45866]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-21048]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Modification of Exclusive Patent License Potent and
Selective Analogues of: Monamine Transporters; Methods of Making; and
Uses Thereof
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The National Institute of Drug Abuse, an institute of the
National Institutes of Health, Department of Health and Human Services
is contemplating the modification of grant of an Exclusive Patent
License to EncepHeal Therapeutics, Inc., located in Winston-Salem,
North Carolina, to practice the inventions embodied in the patent
applications listed in the Supplementary Information section of this
notice.
DATES: Only written comments and/or applications for a license which
are received by the National Institute on Drug Abuse's Technology
Transfer Office on or before October 17, 2017 will be considered.
ADDRESSES: Requests for copies of the patent application, inquiries,
and comments relating to the contemplated modification of the Exclusive
Patent License should be directed to Martha Lubet, Ph.D., Technology
Transfer Manager, NCI TTC, 9609 Medical Center Drive, Room IE350, MSC
9702, Rockville, MD 20850. Telephone: 240 276-5508. Facsimile: 240 276-
5505. Email: lubetm@mail.nih.gov.
SUPPLEMENTARY INFORMATION: The following represents the intellectual
property to be licensed under the prospective agreement:
U.S. provisional application 61/774,878, filed March 8, 2013
entitled ``Potent and Selective Inhibitors of Monamine Transporters;
Methods of Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-US-
01];
PCT application PCT/US2014/021514, filed March 7, 2014 entitled
``Potent and Selective Analogues of: Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-PCT-02];
U.S. application 14/772,486, filed September 3, 2015 entitled
``Potent and Selective Analogues of Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-US-06];
EPO application 14714043.8, filed September 1, 2015 entitled
``Potent and Selective Analogues of Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-EP-05];
Australian application 2014225550, filed September 8, 2015 entitled
``Potent and Selective Analogues of Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-AU-03];
Australian application 2017202849, filed April 28, 2017 entitled
Potent and Selective Analogues of Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-AU-07];
Canadian application 2903746, filed September 2, 2015 entitled
``Potent and Selective Analogues of Monamine Transporters; Methods of
Making; and Uses Thereof'' [HHS Ref. No. E-073-2013/0-CA-04];
The patent rights to these inventions have been assigned to and/or
exclusively licensed to the Government of the United States of America.
The Government previously announced its intention to grant an
exclusive license to EncepHeal at FR 80:245 (December 22, 2015), pp.
79595-79596.
The Notice of Intent to Grant (NOITG) specified a Field of Use as
``Use of
[[Page 45866]]
analogues of monamine transporters to treat substance use disorders and
sleep disorders within the scope of the Licensed Patent Rights''.
Comments/Objections were not received in response to the NOITG. After
consideration, an exclusive license was granted to EncepHeal with a
Licensed Field of Use of: ``Use of analogues of monamine transporters
to treat substance use disorders within the scope of the Licensed
Patent Rights''. This Notice advises the public that the NIH intends to
modify the Licensed Field of Use originally granted to EncepHeal.
Specifically, the National Institute on Drug Abuse is proposing to
modify the Licensed Field of Use to be ``use of a lead compound to
treat one or more of the following: Substance use disorders, cognitive
deficits, sleep disorders, attention deficit hyperactivity disorder and
depressive disorders. The modification to the Licensed Field of Use in
the Exclusive Patent License requires EncepHeal to select a lead
compound for each of the disorders listed in the Field of Use and that
upon selection of a lead compound for a disorder, the other compounds
of the technology will become available for licensing to other
companies.
The technology is directed to novel analogues of modafinil.
Modafinil (marketed as Provisil in United States) is approved by FDA to
treat narcolepsy and other sleep disorders. Modafinil has been studied
as a possible treatment for cognitive dysfunction in disorders such as
attention-deficit hyperactivity disorders (ADHD) as well as cocaine and
methamphetamine addiction. However, it has a relatively low affinity
for dopamine transporter (DAT) and is water-insoluble, thus requiring
large doses to achieve pharmacological effects. Early studies indicated
that modafinil reduced cocaine intake more effectively than placebo;
however, subsequent larger studies reported only modest effectiveness
in reducing cocaine intake. The library of compounds in the technology
are analogs of modafinil and are designed to have higher affinities for
DAT and improved water solubility. The National Institute on Drug Abuse
has conducted preliminary experiments on many of the compounds and has
identified several compounds that have higher affinities than modafinil
for the DAT and lower affinity than modafinil for several other off
target receptors. Preliminary studies at the National Institute on Drug
Abuse indicate that some of the compounds have in vivo activity in
rodents to inhibit cocaine taking behavior and are not selectively
self-administered themselves (i.e. have low abuse liability).
This notice is made in accordance with 35 U.S.C. 209 and 37 CFR
part 404 and incorporates by reference: ``Prospective Grant of
Exclusive Option License: Potent and Selective Analogues of: Monamine
Transporters; Methods of Making; and Uses Thereof'' FR 80:245 (December
22, 2015), pp. 79595-79596. The prospective modification of the
Exclusive Patent License will be royalty bearing and may be granted
unless within fifteen (15) days from date of this published notice, the
National Institute on Drug Abuse receives written evidence and argument
that establishes that the grant of modification to the license would
not be consistent with the requirements of 35 U.S.C. 209 and 37 CFR
Part 404.
Complete applications for a license in the field of use filed in
response to this notice will be treated as objections to the grant of
the contemplated modification to Exclusive Patent License. Comments and
objections submitted 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: September 22, 2107.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer
Institute.
[FR Doc. 2017-21048 Filed 9-29-17; 8:45 am]
BILLING CODE 4040-01-P