National Institute on Aging; Notice of Meeting, 80565-80566 [2022-28457]
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Federal Register / Vol. 87, No. 250 / Friday, December 30, 2022 / Notices
‘‘T Cell Receptors Recognizing MHC
Class II–Restricted Mage–A3’’ [HHS
Reference No. E–230–2012–0–EP–70];
and
54. United States Patent Application
No. 17/936,006 filed September 28,
2022, entitled ‘‘T Cell Receptors
Recognizing MHC Class II–Restricted
Mage–A3’’ [HHS Reference No. E–230–
2012–0–US–82].
(and U.S. and foreign patent
applications claiming priority to the
aforementioned applications)
The patent rights in these inventions
have been assigned and/or exclusively
licensed to the government of the
United States of America.
The prospective exclusive license
territory may be worldwide, and the
field of use may be limited to the
following:
‘‘Development, manufacture and
commercialization of allogeneic Natural
Killer (NK) cell therapy products
engineered to express a therapeutic T
cell receptor claimed in the Licensed
Patent Rights for the treatment or
prevention of cancer in humans.
Specifically excluded from this field
of use are Natural Killer T (NKT) cell
therapy products engineered via viral
and non-viral means for the treatment of
human cancers, wherein the NKT cell
therapy product contains at least 50%
NKT cells.’’
Intellectual Property Group A is
primarily directed to isolated T cell
receptors (TCRs) reactive to mutated
Kirsten rat sarcoma viral oncogene
homolog (KRAS), within the context of
several human leukocyte antigens
(HLAs). Mutated KRAS, which plays a
well-defined driver role in oncogenesis,
is expressed by a variety of human
cancers, including pancreatic, lung,
endometrial, ovarian and prostate. Due
to its restricted expression in
precancerous and cancerous cells, this
antigen may be targeted on mutant
KRAS-expressing tumors with minimal
normal tissue toxicity.
Intellectual Property Group B is
primarily directed to isolated TCRs
reactive to mutated tumor protein 53
(TP53 or P53), within the context of
several HLAs. P53 is the archetypal
tumor suppressor gene and the most
frequently mutated gene in cancer.
Contemporary estimates suggest that
>50% of all tumors carry mutations in
P53. Because of its prevalence in cancer
and its restricted expression to
precancerous and cancerous cells, this
antigen may be targeted on mutant P53expressing tumors with minimal normal
tissue toxicity.
Intellectual Property Group C is
primarily directed to isolated TCRs
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reactive to the E7 oncoprotein of Human
Papilloma Virus (HPV) type 16, within
the context of HLA–A*02. E7
oncoprotein drives malignant
transformation in HPV-infected cells.
Due to its specific and constitutive
expression in cancer cells, this antigen
may be targeted in HPV-positive
malignancies, such as cervical
carcinoma and oropharyngeal
carcinoma, with minimal normal tissue
toxicity.
Intellectual Property Group D is
primarily directed to isolated TCRs
reactive to Melanoma-associated
antigens 3, 6 and 12 (MAGE–A3/A6/
A12), within the context of multiple
HLAs. There are twelve MAGE–A
superfamily antigens designated A1–
A12. These antigens are among the most
commonly expressed cancer testis
antigens in a variety of tumors and are
associated with poor disease prognosis.
They are not expressed on normal cells
other than non-MHC expressing germ
cells of the testis, which do not generate
an immune response. Thus, these
antigens may be targeted on MAGE–Aexpressing tumors with minimal normal
tissue toxicity.
This notice is made in accordance
with 35 U.S.C. 209 and 37 CFR part 404.
The prospective exclusive license will
be royalty bearing, and the prospective
exclusive license may be granted unless
within fifteen (15) days from the date of
this published notice, the National
Cancer Institute 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.
In response to this Notice, the public
may file comments or objections.
Comments and objections, other than
those in the form of a license
application, will not be treated
confidentially, and may be made
publicly available.
License applications submitted in
response to this Notice will be
presumed to contain business
confidential information and any release
of information in these license
applications will be made only as
required and upon a request under the
Freedom of Information Act, 5 U.S.C.
552.
Dated: December 23, 2022.
Richard U. Rodriguez,
Associate Director, Technology Transfer
Center, National Cancer Institute.
[FR Doc. 2022–28404 Filed 12–29–22; 8:45 am]
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80565
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the National Advisory
Council on Aging.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the 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 Advisory
Council on Aging.
Date: September 19–20, 2023.
Closed: September 19, 2023, 3:00 p.m. to
5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, 7201 Wisconsin Avenue,
Bethesda, MD 20892 (Virtual Meeting).
Open: September 20, 2023, 10:00 a.m. to
2:00 p.m.
Agenda: Call to order and report from the
Director; Discussion of future meeting dates;
Consideration of minutes of last meeting;
Reports from Task Force on Minority Aging
Research, Working Group on Program;
Council Speaker; Program Highlights.
Place: National Institute on Aging,
Gateway Building, 7201 Wisconsin Avenue,
Bethesda, MD 20892 (Virtual Meeting).
Closed: September 20, 2023, 2:00 p.m. to
2:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, 7201 Wisconsin Avenue,
Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Kenneth Santora, Ph.D.,
Director, Office of Extramural Activities,
National Institute on Aging, National
Institutes of Health, Gateway Building, 7201
Wisconsin Avenue, Bethesda, MD 20814,
(301) 496–9322, ksantora@nih.gov.
Information is also available on the
Institute’s/Center’s home page:
www.nia.nih.gov/about/naca, where an
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Federal Register / Vol. 87, No. 250 / Friday, December 30, 2022 / Notices
agenda and any additional information for
the meeting will be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.866, Aging Research,
National Institutes of Health, HHS)
Dated: December 27, 2022.
Miguelina Perez,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2022–28457 Filed 12–29–22; 8:45 am]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
[FWS–HQ–LE–2022–N071; FF09L00000/FX/
LE18110900000/223; OMB Control Number
1018–0092]
Agency Information Collection
Activities; Submission to the Office of
Management and Budget for Review
and Approval; Federal Fish and
Wildlife Applications and Reports—
Law Enforcement
Fish and Wildlife Service,
Interior.
ACTION: Notice of information collection;
request for comment.
AGENCY:
In accordance with the
Paperwork Reduction Act of 1995, we,
the U.S. Fish and Wildlife Service
(Service), are proposing to revise an
existing information collection.
DATES: Interested persons are invited to
submit comments on or before January
30, 2023.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under Review—Open for
Public Comments’’ or by using the
search function. Please provide a copy
of your comments to the Service
Information Collection Clearance
Officer, U.S. Fish and Wildlife Service,
MS: PRB (JAO/3W), 5275 Leesburg Pike,
Falls Church, VA 22041–3803 (mail); or
by email to Info_Coll@fws.gov. Please
reference ‘‘1018–0092’’ in the subject
line of your comments.
FOR FURTHER INFORMATION CONTACT: To
request additional information about
this ICR, contact Madonna L. Baucum,
Service Information Collection
Clearance Officer, by email at Info_
Coll@fws.gov, or by telephone at (703)
358–2503. Individuals in the United
States who are deaf, deafblind, hard of
hearing, or have a speech disability may
dial 711 (TTY, TDD, or TeleBraille) to
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access telecommunications relay
services. Individuals outside the United
States should use the relay services
offered within their country to make
international calls to the point-ofcontact in the United States.
SUPPLEMENTARY INFORMATION: In
accordance with the Paperwork
Reduction Act (PRA, 44 U.S.C. 3501 et
seq.) and its implementing regulations
at 5 CFR 1320.8(d)(1), all information
collections require approval under the
PRA. We may not conduct or sponsor
and you are not required to respond to
a collection of information unless it
displays a currently valid OMB control
number.
On September 23, 2022, we published
in the Federal Register (87 FR 58122) a
notice of our intent to request that OMB
approve this information collection. In
that notice, we solicited comments for
60 days, ending on November 22, 2022.
In an effort to increase public awareness
of, and participation in, our public
commenting processes associated with
information collection requests, the
Service also published the Federal
Register notice on Regulations.gov
(Docket No. HQ–LE–2022–0119–0001)
to provide the public with an additional
method to submit comments (in
addition to the typical Info_Coll@
fws.gov email and U.S. mail submission
methods). We received one comment in
response to that notice which did not
address the information collection
requirements. No response is required.
As part of our continuing effort to
reduce paperwork and respondent
burdens, we invite the public and other
Federal agencies to comment on new,
proposed, revised, and continuing
collections of information. This helps us
assess the impact of our information
collection requirements and minimize
the public’s reporting burden. It also
helps the public understand our
information collection requirements and
provide the requested data in the
desired format.
We are especially interested in public
comment addressing the following:
(1) Whether or not the collection of
information is necessary for the proper
performance of the functions of the
agency, including whether or not the
information will have practical utility;
(2) The accuracy of our estimate of the
burden for this collection of
information, including the validity of
the methodology and assumptions used;
(3) Ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) How might the agency minimize
the burden of the collection of
information on those who are to
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respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology, e.g., permitting
electronic submission of response.
Comments that you submit in
response to this notice are a matter of
public record. We will include or
summarize each comment in our request
to OMB to approve this ICR. Before
including your address, phone number,
email address, or other personal
identifying information in your
comment, you should be aware that
your entire comment—including your
personal identifying information—may
be made publicly available at any time.
While you can ask us in your comment
to withhold your personal identifying
information from public review, we
cannot guarantee that we will be able to
do so.
Abstract: The Endangered Species Act
(ESA; 16 U.S.C. 1531 et seq.) makes it
unlawful to import or export wildlife or
wildlife products for commercial
purposes without first obtaining an
import/export license (see 16 U.S.C.
1538(d)). The ESA also requires that fish
or wildlife be imported into or exported
from the United States only at a
designated port, or at a nondesignated
port under certain limited
circumstances (see 16 U.S.C. 1538(f)).
This information collection includes the
following permit/license application
forms:
FWS Form 3–200–2, ‘‘Designated Port
Exception Permit’’
Under 50 CFR 14.11, it is unlawful to
import or export wildlife or wildlife
products at ports other than those
designated in 50 CFR 14.12, unless you
qualify for an exception. The following
exceptions allow qualified individuals,
businesses, or scientific organizations to
import or export wildlife or wildlife
products at a nondesignated port:
(a) To export the wildlife or wildlife
products for scientific purposes;
(b) To minimize deterioration or loss;
or
(c) To relieve economic hardship.
To request authorization to import or
export wildlife or wildlife products at
nondesignated ports, applicants must
complete FWS Form 3–200–2.
Designated port exception permits can
be valid for up to 2 years. We may
require a permittee to file a report on
activities conducted under authority of
the permit.
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[Federal Register Volume 87, Number 250 (Friday, December 30, 2022)]
[Notices]
[Pages 80565-80566]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-28457]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of Meeting
Pursuant to section 10(d) of the Federal Advisory Committee Act, as
amended, notice is hereby given of a meeting of the National Advisory
Council on Aging.
The meeting will be open to the public as indicated below, with
attendance limited to space available. Individuals who plan to attend
and need special assistance, such as sign language interpretation or
other reasonable accommodations, should notify the Contact Person
listed below in advance of the 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 Advisory Council on Aging.
Date: September 19-20, 2023.
Closed: September 19, 2023, 3:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institute on Aging, Gateway Building, 7201
Wisconsin Avenue, Bethesda, MD 20892 (Virtual Meeting).
Open: September 20, 2023, 10:00 a.m. to 2:00 p.m.
Agenda: Call to order and report from the Director; Discussion
of future meeting dates; Consideration of minutes of last meeting;
Reports from Task Force on Minority Aging Research, Working Group on
Program; Council Speaker; Program Highlights.
Place: National Institute on Aging, Gateway Building, 7201
Wisconsin Avenue, Bethesda, MD 20892 (Virtual Meeting).
Closed: September 20, 2023, 2:00 p.m. to 2:30 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institute on Aging, Gateway Building, 7201
Wisconsin Avenue, Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Kenneth Santora, Ph.D., Director, Office of
Extramural Activities, National Institute on Aging, National
Institutes of Health, Gateway Building, 7201 Wisconsin Avenue,
Bethesda, MD 20814, (301) 496-9322, [email protected].
Information is also available on the Institute's/Center's home
page: www.nia.nih.gov/about/naca, where an
[[Page 80566]]
agenda and any additional information for the meeting will be posted
when available.
(Catalogue of Federal Domestic Assistance Program Nos. 93.866, Aging
Research, National Institutes of Health, HHS)
Dated: December 27, 2022.
Miguelina Perez,
Program Analyst, Office of Federal Advisory Committee Policy.
[FR Doc. 2022-28457 Filed 12-29-22; 8:45 am]
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