Request for Information: Establish a Public-Private Collaboration, “Drug Development Initiative” (DDI), for New Pharmacological Treatments for Post-Traumatic Stress Disorder (PTSD), 71211 [2012-28917]
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Federal Register / Vol. 77, No. 230 / Thursday, November 29, 2012 / Notices
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[FR Doc. 2012–28895 Filed 11–28–12; 8:45 am]
BILLING CODE 4830–01–P
DEPARTMENT OF VETERANS
AFFAIRS
Request for Information: Establish a
Public-Private Collaboration, ‘‘Drug
Development Initiative’’ (DDI), for New
Pharmacological Treatments for PostTraumatic Stress Disorder (PTSD)
Office of Research and
Development (ORD).
ACTION: Notice.
AGENCY:
The Department of Veterans
Affairs (VA) ORD publishes this Request
for Information (RFI) to solicit interest
in forming public-private collaborations
to develop new pharmacological
treatments for PTSD. ORD is interested
in developing collaborations with
organizations that are interested in
pursuing clinical trials specifically
focused on PTSD. Such research would
be detailed through a Cooperative
Research and Development Agreement
(CRADA) under the authority of the
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SUMMARY:
VerDate Mar<15>2010
15:12 Nov 28, 2012
Jkt 229001
Federal Technology Transfer Act of
1986 (FTTA), Public Law 99–502,
codified as amended in scattered
sections of title 15, United States Code
(U.S.C.). The CRADA will delineate the
collaboration for PTSD treatment
intended to test new drugs to benefit
Veterans.
This notice will remain open to
accept inquiries and responses.
FOR FURTHER INFORMATION CONTACT:
Interested parties should contact
Theresa Gleason, Ph.D., Senior Program
Manager, Clinical Science Research and
Development Service at (202) 443–5697
or by email at CLINreview@va.gov to
provide an intention to participate.
Please use the subject line: ‘‘DDI.’’
DATES:
ORD has
long supported a robust research
portfolio of studies focused on
understanding and treating PTSD, a
disorder prevalent in Veterans. VA
research has contributed extensively to
advancing knowledge regarding the
neurobiological underpinnings and
leading advances in treatment research
through clinical trials, especially in the
area of psychotherapeutic approaches.
Our program has the capability to
conduct small/early to large/definitive
multi-site clinical trials with the
support of the VA Cooperative Studies
Program. To identify and test new drug
therapies for PTSD and to address the
continuing need to treat Veterans with
this disorder is of high interest to VA.
This RFI is an invitation for responses
from entities interested in participating
in this DDI focused on new
pharmacological treatments for PTSD.
Collaborations will be delineated via
a CRADA under the authority of the
FTTA at 15 U.S.C. 3710a. Under the
FTTA, VA and the entity may exchange
personnel, services, facilities,
equipment, intellectual property, or
other resources. No Federal funds may
be provided to any third party
collaborator, but the VA laboratory is
authorized to accept funds. VA may
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00045
Fmt 4703
Sfmt 9990
71211
grant to the collaborator party a license
or an assignment to inventions made
under the CRADA. We will select
collaborators based on a mutually
beneficial relationship that is fair and
equitable and scientifically sound with
the goal of advancing treatment for
PTSD.
Responses to this RFI should include
the following information:
a. Company profile;
b. Name, contact, and function of
company representative; and
c. Brief rationale for proposed
compound as candidate to be tested as
new treatment for PTSD. Please do not
include proprietary, classified,
confidential, or sensitive information in
your response, but provide scientific
basis for the use of the compound and
the general status of testing completed
to date in human subjects (if any).
We will evaluate DDI responses for
interest. Selected potential collaborators
may be invited to discussions to
develop a CRADA and plan potential
trials. Non-selected respondents will not
receive additional feedback other than a
non-selected notice. Special
consideration will be given to small
business firms and consortia involving
small business firms. Preference will be
given to businesses located in the
United States which agree that products
embodying inventions made under the
CRADA will be manufactured
substantially in the United States as
provided for in 15 U.S.C. 3710a(c)(4).
This RFI does not obligate VA to enter
into a CRADA with any respondent. VA
reserves the right to establish a CRADA
based on scientific analysis and
capabilities found by way of this
announcement or other searches if
determined to be in the best interest of
the government.
Approved: November 26, 2012.
John R. Gingrich,
Chief of Staff, Department of Veterans Affairs.
[FR Doc. 2012–28917 Filed 11–28–12; 8:45 am]
BILLING CODE 8320–01–P
E:\FR\FM\29NON1.SGM
29NON1
Agencies
[Federal Register Volume 77, Number 230 (Thursday, November 29, 2012)]
[Notices]
[Page 71211]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-28917]
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DEPARTMENT OF VETERANS AFFAIRS
Request for Information: Establish a Public-Private
Collaboration, ``Drug Development Initiative'' (DDI), for New
Pharmacological Treatments for Post-Traumatic Stress Disorder (PTSD)
AGENCY: Office of Research and Development (ORD).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Department of Veterans Affairs (VA) ORD publishes this
Request for Information (RFI) to solicit interest in forming public-
private collaborations to develop new pharmacological treatments for
PTSD. ORD is interested in developing collaborations with organizations
that are interested in pursuing clinical trials specifically focused on
PTSD. Such research would be detailed through a Cooperative Research
and Development Agreement (CRADA) under the authority of the Federal
Technology Transfer Act of 1986 (FTTA), Public Law 99-502, codified as
amended in scattered sections of title 15, United States Code (U.S.C.).
The CRADA will delineate the collaboration for PTSD treatment intended
to test new drugs to benefit Veterans.
DATES: This notice will remain open to accept inquiries and responses.
FOR FURTHER INFORMATION CONTACT: Interested parties should contact
Theresa Gleason, Ph.D., Senior Program Manager, Clinical Science
Research and Development Service at (202) 443-5697 or by email at
CLINreview@va.gov to provide an intention to participate. Please use
the subject line: ``DDI.''
SUPPLEMENTARY INFORMATION: ORD has long supported a robust research
portfolio of studies focused on understanding and treating PTSD, a
disorder prevalent in Veterans. VA research has contributed extensively
to advancing knowledge regarding the neurobiological underpinnings and
leading advances in treatment research through clinical trials,
especially in the area of psychotherapeutic approaches. Our program has
the capability to conduct small/early to large/definitive multi-site
clinical trials with the support of the VA Cooperative Studies Program.
To identify and test new drug therapies for PTSD and to address the
continuing need to treat Veterans with this disorder is of high
interest to VA. This RFI is an invitation for responses from entities
interested in participating in this DDI focused on new pharmacological
treatments for PTSD.
Collaborations will be delineated via a CRADA under the authority
of the FTTA at 15 U.S.C. 3710a. Under the FTTA, VA and the entity may
exchange personnel, services, facilities, equipment, intellectual
property, or other resources. No Federal funds may be provided to any
third party collaborator, but the VA laboratory is authorized to accept
funds. VA may grant to the collaborator party a license or an
assignment to inventions made under the CRADA. We will select
collaborators based on a mutually beneficial relationship that is fair
and equitable and scientifically sound with the goal of advancing
treatment for PTSD.
Responses to this RFI should include the following information:
a. Company profile;
b. Name, contact, and function of company representative; and
c. Brief rationale for proposed compound as candidate to be tested
as new treatment for PTSD. Please do not include proprietary,
classified, confidential, or sensitive information in your response,
but provide scientific basis for the use of the compound and the
general status of testing completed to date in human subjects (if any).
We will evaluate DDI responses for interest. Selected potential
collaborators may be invited to discussions to develop a CRADA and plan
potential trials. Non-selected respondents will not receive additional
feedback other than a non-selected notice. Special consideration will
be given to small business firms and consortia involving small business
firms. Preference will be given to businesses located in the United
States which agree that products embodying inventions made under the
CRADA will be manufactured substantially in the United States as
provided for in 15 U.S.C. 3710a(c)(4).
This RFI does not obligate VA to enter into a CRADA with any
respondent. VA reserves the right to establish a CRADA based on
scientific analysis and capabilities found by way of this announcement
or other searches if determined to be in the best interest of the
government.
Approved: November 26, 2012.
John R. Gingrich,
Chief of Staff, Department of Veterans Affairs.
[FR Doc. 2012-28917 Filed 11-28-12; 8:45 am]
BILLING CODE 8320-01-P