Prospective Grant of Exclusive License: Development of Autologous Tumor Infiltrating Lymphocyte Adoptive Cells for the Treatment of Lung, Breast, Bladder, and HPV-Positive Cancers, 30080-30081 [2015-12539]
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Federal Register / Vol. 80, No. 100 / Tuesday, May 26, 2015 / Notices
subsequent changes to the Web sites after this
document publishes in the Federal Register.)
Reis, H., and C. Judd, Handbook of Research
Methods in Social and Personality
Psychology, 2nd Ed. New York:
Cambridge University Press (2014).
Kerig, P.K., and D.H. Baucom, (Eds.). Couple
Observational Coding Systems, Mahwah,
NJ: Erlbaum (2004).
Bakeman, R., Behavioral Observation and
Coding, In H.T. Reis & C.M. Judd (Eds.)
Handbook of Research Methods in Social
and Personality Psychology,pp. 138–159.
New York: Cambridge University Press
(2000).
Ewart, C.K., C.B. Taylor, H.C. Kraemer, and
W.S. Agras. ‘‘High Blood Pressure and
Marital Discord: Not Being Nasty Matters
More Than Being Nice,’’ Health
Psychology, 10, pp. 155–163 (1991).
Spitzberg, B.H., and W.R. Cupach, Handbook
of Interpersonal Competence Research,
NY: Springer-Verlag (1989).
Gottman, J.M., What Predicts Divorce? The
Relationship Between Marital Processes
and Marital Outcomes. Hillsdale, NJ:
Erlbaum (1994).
Rohrmann, B., ‘‘Risk Attitude Scales:
Concepts, Questionnaires, Utilizations
[Project Report],’’ University of
Melbourne, Australia. Retrieved from
https://www.rohrmannresearch.net/pdfs/
rohrmann-racreport.pdf (2005).
Dated: May 18, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015–12582 Filed 5–22–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Mandatory Guidelines for Federal
Workplace Drug Testing Programs
Substance Abuse and Mental
Health Services Administration
(SAMHSA), Department of Health and
Human Services.
ACTION: HHS Approval of Entities That
Certify Medical Review Officers (MRO).
AGENCY:
The current version of the
Department of Health and Human
Services (HHS) Mandatory Guidelines
for Federal Workplace Drug Testing
Programs (Mandatory Guidelines),
effective on October 1, 2010, addresses
the role and qualifications of Medical
Review Officers (MROs) and HHS
approval of entities that certify MROs.
Subpart M—Medical Review Officer
(MRO), Section 13.1(b) of the Mandatory
Guidelines, ‘‘Who may serve as an
MRO?’’ states as follows: ‘‘Nationally
recognized entities that certify MROs or
subspecialty boards for physicians
performing a review of Federal
employee drug test results that seek
approval by the Secretary must submit
their qualifications and a sample
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SUMMARY:
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examination. Based on an annual
objective review of the qualifications
and content of the examination, the
Secretary shall annually publish a list in
the Federal Register of those entities
and boards that have been approved.’’
HHS has completed its review of
entities that certify MROs, in
accordance with requests submitted by
such entities to HHS.
The HHS Secretary approves the
following MRO certifying entities that
offer MRO certification through
examination:
American Association of Medical
Review Officers (AAMRO), P.O. Box
12873, Research Triangle Park, NC
27709; Phone: (800) 489–1839; Fax:
(919) 490–1010; Email: cferrell@
aamro.com; Web site: https://
www.aamro.com/.
Medical Review Officer Certification
Council (MROCC), 836 Arlington
Heights Road, #327, Elk Grove
Village, IL 60007; Phone: (847) 631–
0599; Fax: (847) 483–1282; Email:
mrocc@mrocc.org; Web site: https://
www.mrocc.org/.
DATES: HHS approval is effective May
26, 2015.
FOR FURTHER INFORMATION CONTACT:
Jennifer Fan, Pharm.D., J.D., Division of
Workplace Programs (DWP), Center for
Substance Abuse Prevention (CSAP),
Substance Abuse and Mental Health
Services Administration (SAMHSA), 1
Choke Cherry Road, Room 7–1038,
Rockville, MD 20857; Telephone: (240)
276–1759; Email: jennifer.fan@
samhsa.hhs.gov
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
General Medical Sciences Initial Review
Group; Training and Workforce Development
Subcommittee—C.
Date: June 8, 2015.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hotel Monaco Alexandria, 480 King
Street, Alexandria, VA 22314.
Contact Person: Mona R. Trempe, Ph.D.,
Scientific Review Officer, Office of Scientific
Review, National Institute of General Medical
Sciences, National Institutes of Health, 45
Center Drive, Room 3An.12A, Bethesda, MD
20892–4874, 301–594–3998, trempemo@
mail.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. 93.375, Minority Biomedical
Research Support; 93.821, Cell Biology and
Biophysics Research; 93.859, Pharmacology,
Physiology, and Biological Chemistry
Research; 93.862, Genetics and
Developmental Biology Research; 93.88,
Minority Access to Research Careers; 93.96,
Special Minority Initiatives, National
Institutes of Health, HHS)
Dated: May 19, 2015.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–12543 Filed 5–22–15; 8:45 am]
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Dated: May 15, 2015.
Sylvia M. Burwell,
Secretary.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2015–12559 Filed 5–22–15; 8:45 am]
National Institutes of Health
BILLING CODE 4160–20–P
Prospective Grant of Exclusive
License: Development of Autologous
Tumor Infiltrating Lymphocyte
Adoptive Cells for the Treatment of
Lung, Breast, Bladder, and HPVPositive Cancers
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of General Medical
Sciences; Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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
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AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
This is notice, in accordance
with 35 U.S.C. 209 and 37 CFR 404, that
the National Institutes of Health,
Department of Health and Human
Services, is contemplating the grant of
an exclusive patent license to the
current licensee, Lion Biotechnologies,
Inc., which is located in Woodland
Hills, California to practice the
inventions embodied in the following
patent applications and applications
claiming priority to these applications:
SUMMARY:
E:\FR\FM\26MYN1.SGM
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mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 80, No. 100 / Tuesday, May 26, 2015 / Notices
1. U.S. Provisional Patent Application
No. 61/237,889, filed August 26, 2009
entitled ‘‘Adoptive cell therapy with
young T cells’’ (HHS Ref No. E–273–
2009/0–US–01);
2. U.S. Patent No. 8,383,099 issued
February 26, 2013 entitled ‘‘Adoptive
cell therapy with young T cells’’ (HHS
Ref No. E–273–2009/0–US–02);
3. U.S. Patent Application No. 13/
742,541 filed January 16, 2013 entitled
‘‘Adoptive cell therapy with young T
cells’’ (HHS Ref No. E–273–2009/0–US–
03);
4. U.S. Provisional Patent Application
No. 61/466,200 filed March 22, 2011
entitled ‘‘Methods of growing tumor
infiltrating lymphocytes in gaspermeable containers’’ (HHS Ref No. E–
114–2011/0–US–01);
5. PCT Application No. PCT/US2012/
029744 filed March 20, 2012 entitled
‘‘Methods of growing tumor infiltrating
lymphocytes in gas-permeable
containers’’ (HHS Ref No. E–114–2011/
0–US–01);
6. U.S. Patent Application No. 13/
424,646 filed May 20, 2012 entitled
‘‘Methods of growing tumor infiltrating
lymphocytes in gas-permeable
containers’’ (HHS Ref No. E–114–2011/
0–US–01);
7. U.S. Provisional Patent Application
No. 61/846,161 filed July 15, 2013
entitled ‘‘Methods of Preparing Antihuman Papillomavirus Antigen T Cells’’
(HHS Ref No. E–494–2013/0–US–01);
8. PCT Application No. PCT/US2014/
046478 filed July 14, 2014 entitled
‘‘Methods of Preparing Anti-human
Papillomavirus Antigen T Cells’’ (HHS
Ref No. E–494–2013/0–PCT–02);
The patent rights in these inventions
have been assigned to the United States
of America.
The prospective exclusive license
territory may be worldwide and the
field of use may be limited to the use
of the Licensed Patent Rights to
develop, manufacture, distribute, sell
and use unselected whole autologous
tumor infiltrating lymphocyte (TIL)
adoptive cell therapy products for the
treatment of lung, breast, bladder, and
HPV-positive cancers. Specifically
excluded from this license are methods
of generating or using selected
subpopulations of TIL and the use of T
cell receptors isolated from TIL.
DATES: Only written comments and/or
applications for a license which are
received by the NIH Office of
Technology Transfer on or before June
25, 2015 will be considered.
ADDRESSES: Requests for copies of the
patent application, inquiries, comments,
and other materials relating to the
contemplated exclusive license should
VerDate Sep<11>2014
17:50 May 22, 2015
Jkt 235001
be directed to: Whitney A. Hastings,
Ph.D., Senior Licensing and Patenting
Manager, Office of Technology Transfer,
National Institutes of Health, 6011
Executive Boulevard, Suite 325,
Rockville, MD 20852–3804; Telephone:
(301) 451–7337; Facsimile: (301) 402–
0220; Email: hastingw@mail.nih.gov.
Isolating
cells from the tumor infiltrating
lymphocytes (TIL) of a patient tumor
sample provides a suitable initial
lymphocyte culture for further in vitro
manipulations. NIH scientist have
discovered that taking the isolated cells
through one cycle of rapid expansion
(including exposure to IL–2), rather than
multiple cycles, yields lymphocyte
cultures with higher affinity and longer
persistence in patients. In addition, they
have found that through the use of gas
permeable (GP) flasks, they could obtain
large quantities of highly reactive TIL
from patient tumor samples for anticancer immunotherapy. If an adoptive T
cell transfer immunotherapy is to gain
regulatory approval and successfully
treat a wide array of patients, it will
need to be rapid, reliable, and
technically simple. One of the most
critical factors to this approach is the
generation of effective lymphocyte
cultures that will rapidly and repeatedly
attack the target cells when infused into
patients.
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.
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 exclusive
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.
SUPPLEMENTARY INFORMATION:
Dated: May 19, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology
Transfer, National Institutes of Health.
[FR Doc. 2015–12539 Filed 5–22–15; 8:45 am]
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30081
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Request From the Interagency
Committee on Human Nutrition
Research (ICHNR) for Comments on
the Draft National Nutrition Research
Roadmap 2015–2020: Advancing
Nutrition Research To Improve and
Sustain Health
The Draft National Nutrition
Research Roadmap (NNRR) identifies
research priorities for human nutrition
and describes the role of ICHNR
departments and agencies in addressing
those priorities over the next five to ten
years. ICHNR seeks input about
identified research and resource gaps
and opportunities and the short- and
long-term initiatives proposed to
address them. To review the NNRR,
please visit https://prevention.nih.gov/
nnrr.
SUMMARY:
To ensure consideration, your
responses must be received by 11:59
p.m. Eastern Standard Time on June 25,
2015.
ADDRESSES: Responses to this Notice
must be submitted via email to
NNRRfeedback@nih.gov or postal mail
to the National Institutes of Health,
Division of Nutrition Research
Coordination, Two Democracy Plaza,
Room 635, 6707 Democracy
Boulevard—MSC 5461, Bethesda,
Maryland 20892–5461.
FOR FURTHER INFORMATION CONTACT: Dr.
Sheila Fleischhacker, Senior Public
Health & Science Policy Advisor,
National Institutes of Health, Division of
Nutrition Research Coordination, Two
Democracy Plaza, Room 635, 6707
Democracy Boulevard—MSC 5461,
Bethesda, Maryland 20892–5461.
Telephone: 301–594–7440, Fax: 301–
480–3768, Email: NNRRfeedback@
nih.gov.
DATES:
SUPPLEMENTARY INFORMATION:
Background
Improved nutrition could be one of
the most cost-effective approaches to
address many of the societal,
environmental, and economic
challenges facing the nation today,
including the morbidity, mortality, and
economic burden associated with
chronic diseases and disorders. That is,
nutrition plays an integral role in
human growth and development, in the
maintenance of good health and
functionality, and in the prevention and
treatment of infectious, acute and
chronic diseases, as well as genetic
disorders such as inborn errors of
E:\FR\FM\26MYN1.SGM
26MYN1
Agencies
[Federal Register Volume 80, Number 100 (Tuesday, May 26, 2015)]
[Notices]
[Pages 30080-30081]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-12539]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive License: Development of Autologous
Tumor Infiltrating Lymphocyte Adoptive Cells for the Treatment of Lung,
Breast, Bladder, and HPV-Positive Cancers
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This is notice, in accordance with 35 U.S.C. 209 and 37 CFR
404, that the National Institutes of Health, Department of Health and
Human Services, is contemplating the grant of an exclusive patent
license to the current licensee, Lion Biotechnologies, Inc., which is
located in Woodland Hills, California to practice the inventions
embodied in the following patent applications and applications claiming
priority to these applications:
[[Page 30081]]
1. U.S. Provisional Patent Application No. 61/237,889, filed August
26, 2009 entitled ``Adoptive cell therapy with young T cells'' (HHS Ref
No. E-273-2009/0-US-01);
2. U.S. Patent No. 8,383,099 issued February 26, 2013 entitled
``Adoptive cell therapy with young T cells'' (HHS Ref No. E-273-2009/0-
US-02);
3. U.S. Patent Application No. 13/742,541 filed January 16, 2013
entitled ``Adoptive cell therapy with young T cells'' (HHS Ref No. E-
273-2009/0-US-03);
4. U.S. Provisional Patent Application No. 61/466,200 filed March
22, 2011 entitled ``Methods of growing tumor infiltrating lymphocytes
in gas-permeable containers'' (HHS Ref No. E-114-2011/0-US-01);
5. PCT Application No. PCT/US2012/029744 filed March 20, 2012
entitled ``Methods of growing tumor infiltrating lymphocytes in gas-
permeable containers'' (HHS Ref No. E-114-2011/0-US-01);
6. U.S. Patent Application No. 13/424,646 filed May 20, 2012
entitled ``Methods of growing tumor infiltrating lymphocytes in gas-
permeable containers'' (HHS Ref No. E-114-2011/0-US-01);
7. U.S. Provisional Patent Application No. 61/846,161 filed July
15, 2013 entitled ``Methods of Preparing Anti-human Papillomavirus
Antigen T Cells'' (HHS Ref No. E-494-2013/0-US-01);
8. PCT Application No. PCT/US2014/046478 filed July 14, 2014
entitled ``Methods of Preparing Anti-human Papillomavirus Antigen T
Cells'' (HHS Ref No. E-494-2013/0-PCT-02);
The patent rights in these inventions have been assigned to the
United States of America.
The prospective exclusive license territory may be worldwide and
the field of use may be limited to the use of the Licensed Patent
Rights to develop, manufacture, distribute, sell and use unselected
whole autologous tumor infiltrating lymphocyte (TIL) adoptive cell
therapy products for the treatment of lung, breast, bladder, and HPV-
positive cancers. Specifically excluded from this license are methods
of generating or using selected subpopulations of TIL and the use of T
cell receptors isolated from TIL.
DATES: Only written comments and/or applications for a license which
are received by the NIH Office of Technology Transfer on or before June
25, 2015 will be considered.
ADDRESSES: Requests for copies of the patent application, inquiries,
comments, and other materials relating to the contemplated exclusive
license should be directed to: Whitney A. Hastings, Ph.D., Senior
Licensing and Patenting Manager, Office of Technology Transfer,
National Institutes of Health, 6011 Executive Boulevard, Suite 325,
Rockville, MD 20852-3804; Telephone: (301) 451-7337; Facsimile: (301)
402-0220; Email: hastingw@mail.nih.gov.
SUPPLEMENTARY INFORMATION: Isolating cells from the tumor infiltrating
lymphocytes (TIL) of a patient tumor sample provides a suitable initial
lymphocyte culture for further in vitro manipulations. NIH scientist
have discovered that taking the isolated cells through one cycle of
rapid expansion (including exposure to IL-2), rather than multiple
cycles, yields lymphocyte cultures with higher affinity and longer
persistence in patients. In addition, they have found that through the
use of gas permeable (GP) flasks, they could obtain large quantities of
highly reactive TIL from patient tumor samples for anti-cancer
immunotherapy. If an adoptive T cell transfer immunotherapy is to gain
regulatory approval and successfully treat a wide array of patients, it
will need to be rapid, reliable, and technically simple. One of the
most critical factors to this approach is the generation of effective
lymphocyte cultures that will rapidly and repeatedly attack the target
cells when infused into patients.
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.
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 exclusive 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: May 19, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology Transfer, National Institutes of
Health.
[FR Doc. 2015-12539 Filed 5-22-15; 8:45 am]
BILLING CODE 4140-01-P