Agency Information Collection Activities: Submission for OMB Review; Comment Request, 54297-54298 [E6-15240]
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Federal Register / Vol. 71, No. 178 / Thursday, September 14, 2006 / Notices
trade secrets or commercial property
such as patentable material, and
personal information concerning
individuals associated with the grant
applications, the disclosure of which
constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: NIDCR Special Grants
Review Committee, 07–01, Review RO3s, Ks,
Fs.
Date: October 12–13, 2006.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Clarion Hotel Bethesda Park, 8400
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Raj K. Krishnaraju, Ph.D.,
MS, Scientific Review Administrator,
Scientific Review Branch, National Inst of
Dental & Craniofacial Research, National
Institutes of Health, 45 Center Dr. Rm 4AN
32J, Bethesda, MD 20892. 301–594–4864.
kkrishna@nidcr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.121, Oral Diseases and
Disorders Research, National Institutes of
Health, HHS).
Dated: September 5, 2006.
Anna Snouffer,
Acting Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 06–7628 Filed 9–13–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of Exclusive
License: Use of a Complete T-Cell
Receptor Recognizing MART–1
Peptide Restricted by HLA–A2,
Incorporated in a Continuous TLymphocyte Cell Line Developed or
Owned by Licensee To Treat Cancer
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
rwilkins on PROD1PC63 with NOTICES
AGENCY:
SUMMARY: This notice, in accordance
with 35 U.S.C. 209(c)(1) and 37 CFR
part 404.7(a)(1)(i), that the National
Institutes of Health, Department of
Health and Human Services, is
contemplating the grant of an exclusive
patent license to practice the inventions
embodied in U.S. patent 5,830,755 filed
March 27, 1995 [HHS Ref. No. E–093–
1995/0–US–01] and Australian Patent
709122 filed March 27, 1996 [HHS Ref.
No. E–093–1995/0–AU–03], entitled TCell Receptors and Their Use in
Therapeutic and Diagnostic Methods, to
CellCure A/S, which is located in
Aarhus, Denmark. The patent rights in
these inventions have been assigned to
the United States of America.
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The prospective exclusive license
territory may be worldwide and the
field of use may be limited to the use
of a complete T-cell receptor MART–1
peptide restricted by HLA–A2
incorporated into a continuous TLymphocyte cell line developed or
owned by licensee to treat cancer.
Date: September 7, 2006.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. E6–15216 Filed 9–13–06; 8:45 am]
Only written comments and/or
applications for a license which are
received by the NIH Office of
Technology Transfer on or before
November 13, 2006 will be considered.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Requests for copies of the
patent application, inquiries, comments,
and other materials relating to the
contemplated exclusive license should
be directed to: Michelle A. Booden,
Ph.D., Technology Licensing Specialist,
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; e-mail:
boodenm@mail.nih.gov.
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
The
technology describes the composition
and use of nucleic acid sequences that
encode polypeptides capable of forming
a T-cell receptor (TCR) in a genetically
engineered cell. Specifically, these
nucleic acid sequences will encode
TCR’s specific to tumor associated
antigens (TAA), MART–1. T-Cells
engineered with these tumor associated
antigen specific TCRs show specific
immune responses against TAA
expressing cancer cells. Additionally, a
method of treating or preventing cancer
by administrating the above described
TCRs is also disclosed.
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 404.7. The
prospective exclusive license may be
granted unless within sixty (60) 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 404.7.
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.
Project: Measures of Co-Occurring
Infrastructure—NEW
SAMHSA’s Center for Mental Health
Services and Center for Substance
Abuse Treatment will implement
provider-level performance measures
about the screening, assessment, and
treatment of co-occurring disorders.
Implementation will be limited to the 15
current States with Co-occurring State
Incentive Grants (COSIG), and States
receiving COSIG grants in 2006 and
future years. SAMHSA anticipates
awarding two COSIG grants in 2006.
COSIG grants enable States to develop
or enhance their infrastructure and
capacity to provide accessible, effective,
comprehensive, coordinated/integrated,
and evidence-based treatment services
to persons with co-occurring substance
abuse and mental disorders. Only the
immediate Office of the Governor of
States may receive COSIG grants,
because SAMHSA considers the Office
of the Governor to have the greatest
potential to provide the multi-agency
leadership needed to accomplish COSIG
goals. The COSIG program is part of
SAMHSA plan to achieve certain goals
regarding services for persons with cooccurring substance use and mental
disorders:
• Increase percentage of treatment
programs that screen for co-occurring
disorders;
• Increase percentage of treatment
programs that assess for co-occurring
disorders;
• Increase percentage of treatment
programs that treat co-occurring
disorders through collaborative,
DATES:
ADDRESSES:
SUPPLEMENTARY INFORMATION:
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Substance Abuse and Mental Health
Services Administration
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
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Federal Register / Vol. 71, No. 178 / Thursday, September 14, 2006 / Notices
consultative, and integrated models of
care;
• Increase the number of persons
with co-occurring disorders served.
The proposed measures will enable
SAMHSA to benchmark and track
progress toward these goals within
COSIG states.
Information will be collected annually
about the number and percentage of
programs that offer screening,
assessment, and treatment services for
co-occurring disorders; and the number
of clients actually screened, assessed,
and treated through these programs.
Information will also be collected
annually about providers’ policies
regarding screening, assessment, and
treatment services for persons with cooccurring disorders.
A questionnaire, to be completed by
providers, contains 47 items, answered
either by checking a box or entering a
number in a blank. The questionnaire is
available both in printed form and
electronically. Obtaining the
information to enter on the
questionnaire will require respondent
Number of respondents
Data collection
providers to track screening,
assessment, and treatment services for
clients.
COSIG States will be required to
report aggregated information to
SAMHSA for all providers directly
participating in their COSIG projects.
Samhsa will consider sampling
strategies for states with large numbers
of participating providers and for
providers serving large numbers of
clients.
Annual burden for the activities is
shown below:
Responses
per
respondent
Hours
per
response
Total burden
hours
Capacity to Screen, Assess, and Treat ........................................
Policy on Screening, Assessment, Referral, and Treatment .......
242
242
1
1
4.5 .....................................
3 minutes ..........................
1,089
12
Total .......................................................................................
242
........................
...........................................
1,101
Written comments and
recommendations concerning the
proposed information collection should
be sent by October 16, 2006 to:
SAMHSA Desk Officer, Human
Resources and Housing Branch, Office
of Management and Budget, New
Executive Office Building, Room 10235,
Washington, DC 20503; due to potential
delays in OMB’s receipt and processing
of mail sent through the U.S. Postal
Service, respondents are encouraged to
submit comments by fax to: 202–395–
6974.
Dated: September 6, 2006.
Anna Marsh,
Director, Office of Program Services.
[FR Doc. E6–15240 Filed 9–13–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
rwilkins on PROD1PC63 with NOTICES
Agency Information Collection
Activities: Proposed Collection;
Comment Request
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
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Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Proposed Project: GPRA Client
Outcomes for the Substance Abuse and
Mental Health Services Administration
(SAMHSA)—(OMB No. 0930–0208)—
Revision
The mission of the Substance Abuse
and Mental Health Services
Administration (SAMHSA) is to
improve the effectiveness and efficiency
of substance abuse and mental health
treatment and prevention services
across the United States. All of
SAMHSA’s activities are designed to
ultimately reduce the gap in the
availability of substance abuse and
mental health services and to improve
their effectiveness and efficiency.
Data are collected from all SAMHSA
discretionary services grants and
contracts where client/participant
outcomes are to be assessed at three
points (for the Center for Substance
Abuse Treatment (CSAT): Intake,
discharge, and post-intake and for the
Center for Substance Abuse Prevention
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(CSAP): Pre-intervention, postintervention, and follow-up). SAMHSAfunded projects are required to submit
these data as a contingency of their
award. The analysis of the data also will
help determine whether the goal of
reducing health and social costs of drug
use to the public is being achieved.
The primary purpose of this data
collection activity is to meet the
reporting requirements of the
Government Performance and Results
Act (GPRA) by allowing SAMHSA to
quantify the effects and
accomplishments of SAMHSA
programs.
The burden for the Center for Mental
Health Services (CMHS) will be
transferred from this data collection to
its own separate Office of Management
and Budget (OMB) clearance. The 60day Federal Register Notice for National
Outcome Measures (NOMS) for
Consumers Receiving Mental Health
Services was published on Friday, June
9, 2006 (Vol. 71, No. 111, p. 33476).
The burden for the CSAP gradually
reduces due to the fact that this
clearance request only pertains to a
continuation of data collection for those
grantees initially funded prior to
FY2006. The new grantees (FY2006 and
beyond) are approved under the NOMS
for CSAP (OMB No. 0930–0230).
CSAT has no revisions to the
instrument and the data collection time
will remain the same but there is an
increase in the number of respondents
due to identifying the seven Screening,
Brief Intervention, and Referral to
Treatment program grantees that
provide data uploads. The estimated
annual response burden for this effort is
provided in the table below:
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[Federal Register Volume 71, Number 178 (Thursday, September 14, 2006)]
[Notices]
[Pages 54297-54298]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-15240]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Substance Abuse and Mental Health Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and Mental Health Services
Administration (SAMHSA) will publish a summary of information
collection requests under OMB review, in compliance with the Paperwork
Reduction Act (44 U.S.C. Chapter 35). To request a copy of these
documents, call the SAMHSA Reports Clearance Officer on (240) 276-1243.
Project: Measures of Co-Occurring Infrastructure--NEW
SAMHSA's Center for Mental Health Services and Center for Substance
Abuse Treatment will implement provider-level performance measures
about the screening, assessment, and treatment of co-occurring
disorders. Implementation will be limited to the 15 current States with
Co-occurring State Incentive Grants (COSIG), and States receiving COSIG
grants in 2006 and future years. SAMHSA anticipates awarding two COSIG
grants in 2006. COSIG grants enable States to develop or enhance their
infrastructure and capacity to provide accessible, effective,
comprehensive, coordinated/integrated, and evidence-based treatment
services to persons with co-occurring substance abuse and mental
disorders. Only the immediate Office of the Governor of States may
receive COSIG grants, because SAMHSA considers the Office of the
Governor to have the greatest potential to provide the multi-agency
leadership needed to accomplish COSIG goals. The COSIG program is part
of SAMHSA plan to achieve certain goals regarding services for persons
with co-occurring substance use and mental disorders:
Increase percentage of treatment programs that screen for
co-occurring disorders;
Increase percentage of treatment programs that assess for
co-occurring disorders;
Increase percentage of treatment programs that treat co-
occurring disorders through collaborative,
[[Page 54298]]
consultative, and integrated models of care;
Increase the number of persons with co-occurring disorders
served.
The proposed measures will enable SAMHSA to benchmark and track
progress toward these goals within COSIG states.
Information will be collected annually about the number and
percentage of programs that offer screening, assessment, and treatment
services for co-occurring disorders; and the number of clients actually
screened, assessed, and treated through these programs. Information
will also be collected annually about providers' policies regarding
screening, assessment, and treatment services for persons with co-
occurring disorders.
A questionnaire, to be completed by providers, contains 47 items,
answered either by checking a box or entering a number in a blank. The
questionnaire is available both in printed form and electronically.
Obtaining the information to enter on the questionnaire will require
respondent providers to track screening, assessment, and treatment
services for clients.
COSIG States will be required to report aggregated information to
SAMHSA for all providers directly participating in their COSIG
projects. Samhsa will consider sampling strategies for states with
large numbers of participating providers and for providers serving
large numbers of clients.
Annual burden for the activities is shown below:
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total burden
Data collection respondents respondent Hours per response hours
----------------------------------------------------------------------------------------------------------------
Capacity to Screen, Assess, and Treat. 242 1 4.5..................... 1,089
Policy on Screening, Assessment, 242 1 3 minutes............... 12
Referral, and Treatment.
-------------------------------------------------------------------------
Total............................. 242 .............. ........................ 1,101
----------------------------------------------------------------------------------------------------------------
Written comments and recommendations concerning the proposed
information collection should be sent by October 16, 2006 to: SAMHSA
Desk Officer, Human Resources and Housing Branch, Office of Management
and Budget, New Executive Office Building, Room 10235, Washington, DC
20503; due to potential delays in OMB's receipt and processing of mail
sent through the U.S. Postal Service, respondents are encouraged to
submit comments by fax to: 202-395-6974.
Dated: September 6, 2006.
Anna Marsh,
Director, Office of Program Services.
[FR Doc. E6-15240 Filed 9-13-06; 8:45 am]
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