pub 30 day FRN

11549

Federal Register / Vol. 86, No. 36 / Thursday, February 25, 2021 / Notices
clinical utility has been constrained, in
part, by dose-limiting toxicity following
systemic administration and the need
for repeated dosing. The subject
invention addresses these limitations
through synthetic IL–15/21 sequences
which incorporate flexible linker
regions and cell membrane anchors. T
cells engineered to express these
constructs experience autocrine IL–15/
21 signaling leading to enhanced antitumor function in vivo.
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 establishing 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 from 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: February 12, 2021.
Richard U. Rodriguez,
Associate Director, Technology Transfer
Center, National Cancer Institute.
[FR Doc. 2021–03873 Filed 2–24–21; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request; CareerTrac
AGENCY:

National Institutes of Health,

HHS.

ACTION:

after October 1, 1995, unless it displays
a currently valid OMB control number.
In compliance with Section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH) has submitted
to the Office of Management and Budget
(OMB) a request for review and
approval of the information collection
listed below.
Proposed Collection: CareerTrac0925–0568—expiration date April 30,
2021, REVISION, Fogarty International
Center (FIC), National Institute of
Environmental Health Sciences
(NIEHS), National Cancer Institute
(NCI), National Institute of Diabetes and
Digestive Kidney Diseases, (NIDDK),
National Institutes of Health (NIH).
Need and Use of Information
Collection: The purpose of this data
collection system is to track, evaluate
and report short and long-term outputs,
outcomes and impacts of trainees
involved in health research training
programs-specifically tracking this for at
least ten years following training by
having Principal Investigators enter data
after trainees have completed the
program. The data collection system
provides a streamlined, web-based
application permitting principal
investigators to record career
achievement progress by trainee on a
voluntary basis. FIC, NCI, NIDDK, and
NIEHS management will use this data to
monitor, evaluate and adjust grants to
ensure desired outcomes are achieved,
comply with OMB Part requirements,
respond to congressional inquiries, and
as a guide to inform future strategic and
management decisions regarding the
grant program.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
12,705.

Notice.

In compliance with the
Paperwork Reduction Act of 1995, the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 30-days of the date of this
publication.
SUMMARY:

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 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Dr. Kristi
Pettibone, Health Scientist
Administrator, Program Analysis
Branch, Division of Extramural Research
and Training, NIEHS, NIH, 560 Davis
Dr., Morrisville, NC 27560, or call nontoll-free number (984) 287–3303 or
Email your request, including your
address to: pettibonekg@niehs.nih.gov.
SUPPLEMENTARY INFORMATION: This
proposed information collection was
previously published in the Federal
Register on December 12, 2020, page
79493–79494 (64 FR 15367) and
allowed 60 days for public comment. No
public comments were received. The
purpose of this notice is to allow an
additional 30 days for public comment.
The Fogarty International Center (FIC),
National Cancer Institute (NCI),
National Institute of Diabetes and
Digestive and Kidney Diseases (NIDDK),
and National Institute of Environmental
Health Sciences (NIEHS), may not
conduct or sponsor, and the respondent
is not required to respond to, an
information collection that has been
extended, revised, or implemented on or
ADDRESSES:

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondent

FIC Grantee .....................................................................................................
NIEHS Grantee ................................................................................................
NCI CRCHD Grantee ......................................................................................
NCI D43 Grantee .............................................................................................
Superfund Grantee ..........................................................................................

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Number of
responses per
respondent

90
60
244
20
30

E:\FR\FM\25FEN1.SGM

20
45
22
22
105

25FEN1

Average
burden per
response
(in hours)
40/60
40/60
40/60
40/60
40/60

Total annual
burden hour
1,200
1,800
3,579
293
2,100

11550

Federal Register / Vol. 86, No. 36 / Thursday, February 25, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents

Type of respondent

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total annual
burden hour

NIDDK Grantee ................................................................................................
Trainees ...........................................................................................................

30
5,000

20
1

40/60
40/60

400
3,333

Total ..........................................................................................................

5,474

19,058

........................

12,705

Jane M. Lambert,
Project Clearance Liaison, National Institute
of Environmental Health Sciences, National
Institutes of Health.
[FR Doc. 2021–03871 Filed 2–24–21; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60 Day Comment
Request; The Impact of Clinical
Research Training and Medical
Education at the Clinical Center on
Physician Careers in Academia and
Clinical Research (Clinical Center)
AGENCY:

National Institutes of Health,

HHS.
ACTION:

Notice.

In compliance with the
requirement of the Paperwork
Reduction Act of 1995, for opportunity
for public comment on proposed data
collection projects, the Clinical Center,
the National Institutes of Health (NIH)
will publish periodic summaries of
proposed projects to be submitted to the
Office of Management and Budget
(OMB) for review and approval.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 60 days of the date of this
publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
SUMMARY:

Medical Education at the Clinical Center
on Physician Careers in Academia and
Clinical Research, OMB #0925–0602
Expiration Date: 11/30/2022, REVISION,
Clinical Center (CC), National Institutes
of Health (NIH).
Need and Use of Information
Collection: The information collected
will allow continued assessment of the
value of the training provided by the
Office of Clinical Research Training and
Medical Education (OCRTME) at the
NIH Clinical Center and the extent to
which this training promotes (a) patient
safety; (b) research productivity and
independence; and (c) future career
development within clinical,
translational, and academic research
settings. The information received from
respondents is presented to, evaluated
by, and incorporated into the ongoing
operational improvement efforts of the
Director of the Office of Clinical
Research Training and Education, and
the Chief Executive Officer of the NIH
Clinical Center. This information will
enable the ongoing operational
improvement efforts of the OCRTME
and its commitment to providing
clinical research training and medical
education of the highest quality to each
trainee.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours 478.

plans and instruments, contact: Robert
M. Lembo, MD, Office of Clinical
Research Training and Medical
Education, NIH Clinical Center,
National Institutes of Health, 10 Center
Drive, Room 1N252C, Bethesda, MD
20892–1158, or call non-toll-free
number (301) 496–2636, or Email your
request, including your address to:
robert.lembo@nih.gov. Formal requests
for additional plans and instruments
must be requested in writing.
SUPPLEMENTARY INFORMATION: Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: Written
comments and/or suggestions from the
public and affected agencies are invited
to address one or more of the following
points: (1) Whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) The accuracy of the
agency’s estimate of the burden of the
proposed 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) Ways to minimizes
the burden of the collection of
information on those who are to
respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Proposed Collection Title: The Impact
of Clinical Research Training and

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Form name

Number of
responses per
respondent

Average
burden
per response
(in hours)

Total annual
burden hours
requested

CRTP/MRSP Alumni Survey ...........................................................................
Summer Internship Program Alumni Survey ...................................................
Graduate Medical Education Graduate Survey ...............................................
Clinical Electives Program 1 Year Alumni Surveys .........................................

704
280
350
100

1
1
1
1

20/60
20/60
20/60
20/60

235
93
117
33

Total ..........................................................................................................

1,434

1,434

........................

478

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