Announcement of Requirements and Registration for: “Harnessing Insights From Other Disciplines To Advance Drug Abuse and Addiction Research” Challenge, 30084-30087 [2015-12632]
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Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3148,
MSC 7770, Bethesda, MD 20892, (301) 254–
9975, helmersk@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; RFA–RM–
14–030: Nuclear Organization and Function
Interdisciplinary Consortium (NOFIC) (U54).
Date: June 24–25, 2015.
Time: 8:00 a.m. to 3:00 p.m.
Agenda: To review and evaluate grant
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Contact Person: Kee Hyang Pyon, Ph.D.,
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csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; SBIR/STTR
Informatics.
Date: June 24, 2015.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
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Place: National Institutes of Health, 6701
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Contact Person: Melinda Jenkins, Ph.D.,
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Review Special Emphasis Panel; PAR–14–
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Agenda: To review and evaluate grant
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Dated: May 19, 2015.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–12546 Filed 5–22–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Announcement of Requirements and
Registration for: ‘‘Harnessing Insights
From Other Disciplines To Advance
Drug Abuse and Addiction Research’’
Challenge
Authority: 15 U.S.C. 3719.
The National Institute on
Drug Abuse (NIDA), a component of the
National Institutes of Health (NIH), is
seeking from the general public ideas on
how to adapt specialized knowledge
from other disciplines to inform new
directions and discoveries in drug abuse
and addiction research. With the
‘‘Harnessing insights from other
disciplines to advance drug abuse and
addiction research’’ challenge (the
‘‘Challenge’’), NIDA aims to gain
insights into new methods or
approaches that could transform
discovery in order to significantly
expand our basic knowledge about drug
abuse and addiction processes,
accelerate the development of novel and
more effective prevention and treatment
strategies, and/or enhance our capacity
to implement, monitor, and improve
upon evidence-based interventions.
This Challenge is soliciting written
proposals that outline novel approaches
to addressing research challenges in the
drug use and addiction field by
leveraging concepts or technologies
from other disciplines. This Challenge is
being issued as part of NIDA’s strategic
planning process for 2016–2020.
Winning proposals may be used to
guide the development of new research
programs within NIDA.
DATES:
(1) Submission Period begins May 26,
2015, 9:00 a.m., EST
(2) Submission Period ends June 22,
2015, 11:59 p.m., EST
(3) Judging Period June 23, 2015 to July
17, 2015
(4) Winners Announced July 30, 2015
FOR FURTHER INFORMATION CONTACT: Dr.
Emily Einstein, Ph.D., Science Policy
Branch, Office of Science Policy and
Communication, National Institute on
Drug Abuse, Phone: 301–443–6071,
Email: emily.einstein@nih.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Subject of the Challenge
For the past four decades, the
National Institute on Drug Abuse
(NIDA) has led the way in supporting
research to prevent and treat drug abuse
and addiction and to mitigate the
impact of their consequences, which
include the spread of HIV/AIDS and
other infectious diseases. To confront
the most pressing aspects of the
complex disease of addiction and to
tackle its underlying causes, NIDA’s
strategic approach is multipronged and
includes research programs in basic,
clinical, and translational sciences.
These programs support studies in
genetics, functional neuroimaging,
social neuroscience, medication and
behavioral therapies, prevention, and
health services, including costeffectiveness research. NIDA’s evolving
portfolio has produced a vast body of
knowledge that informs strategic
directions for future research, and this
Challenge represents a new approach to
broaden the pool of testable ideas.
Scientific knowledge about drug
addiction and its treatment has
increased markedly over the past couple
of decades. Today, we have a better
understanding of the effects of drugs on
the brain, as well as new and more
effective treatments than were available
in the past. A changing healthcare
landscape may provide opportunities to
further enhance the quality of addiction
prevention and treatment. Still,
addiction remains a pressing public
health issue, and this Challenge seeks to
accelerate progress in the field of drug
abuse and addiction research by
incentivizing a broader community of
stakeholders—including those not
formally involved in biomedical or
addiction-related disciplines—to
propose new ideas or innovations that
leverage concepts or technologies from
other disciplines to advance drug abuse
and addiction research.
While preparing their proposals,
applicants should bear in mind NIDA’s
traditional priority areas, persistent
roadblocks that hamper progress, and
evolving and emerging opportunities.
Some illustrative examples are
discussed below; however, proposals
may address any challenge within the
drug use and addiction field.
NIDA priority areas. NIDA’s charge, to
bring the power of science to bear on
drug abuse and addiction, has two
critical components. The first is the
strategic support and conduct of
research across a broad range of
disciplines. The second is ensuring the
rapid and effective dissemination and
implementation of the results of that
research to significantly improve
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prevention and treatment and to inform
policy as it relates to drug use and
addiction. These aims are currently met
by a broad range of projects in basic,
clinical, and translational sciences. For
more information on current NIDA
research programs please visit
www.drugabuse.gov.
Roadblocks to progress in addiction
research and its translation. There are
many scientific and non-scientific
roadblocks that hamper progress on
drug use and addiction research. For
example, one of the most frequently
cited obstacles to clinical advances in
the field of drug use disorders is the
lack of interest by the pharmaceutical
industry in developing new addiction
medications. This is largely due to the
low success rate of clinical trials for
neurotherapeutics and the perceived
lack of financial incentives to pursue
new pharmacotherapies for substance
use disorders. Other key obstacles
include the reluctance of some primary
care providers to address substance
abuse with their patients. On the basic
research side, reproducibility,
transparency, data sharing, and training
a diverse workforce remain areas in
need of improvement.
Emerging Opportunities. New
discoveries, technologies, paradigms,
and ways of thinking play a key role in
our efforts to understand addiction, to
develop better ways to influence
addiction trajectories, and to mitigate its
consequences. The examples below are
meant to illustrate just a few areas of
rapidly evolving technologies and
emerging opportunities from which the
drug use and addiction field expects to
reap significant benefits in the near
future.
Genomics and Epigenomics. Recent
technological developments have led to
important advances in linking genes and
their regulation with behavior. We now
have an unprecedented capacity to
screen for thousands of genetic and
epigenetic variations and catalogue how
they modulate substance use disorder
risk by influencing gene expression,
brain maturation, neural architecture,
and behavioral patterns. In addition,
advances in epigenetics research are
enabling increased understanding of
how environmental factors (e.g.,
parenting style, drug exposure) can
affect the expression of specific genes to
either strengthen or weaken risk for
substance use and addiction. Similar
approaches could be applied to leverage
advances in metabolomics, proteomics,
connectomes, transcriptomics and
systems biology to better characterize
the role of these systems in drug use and
addiction.
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Big Data. Behavioral disorders
including drug use disorders are
incredibly complex, with multiple
biological, environmental, and
developmental factors contributing to
risk. Very large data sets (on the scale
of tera- or petabytes, typically referred
to as ‘‘Big Data’’) sets are essential
platforms for the analysis of such
complex systems, overlaying genetic,
molecular, cellular, environmental,
behavioral, and structural and
functional brain imaging data. Big Data
also brings analysis opportunities in
many other areas, such as social media
and socio-economic mapping which,
when combined with health
information, could lead to an improved
understanding of predictors of
psychiatric illness risk (including
addiction), trajectory, and treatment
responses. This area of development
presents significant opportunities for
innovation for research.
Data Sharing. Data sharing is a critical
component that allows the results of
NIDA’s research to be distributed to
investigators and the public in order to
promote new research, encourage
further analyses, and disseminate
information to the community.
Secondary analyses of shared data
multiply the scientific contribution of
the original research. The development
of new strategies to facilitate effective
data sharing and analysis is one area in
which new ideas could spur significant
advancement.
Informatics. NIDA is already pursuing
several avenues to realize the research
and clinical potential of various
informatics tools. Notable examples
include:
Æ Development of a comprehensive
clinical decision support systems based
on advanced database analysis
techniques.
Æ Research in theoretical and applied
areas of medical and clinical
informatics, including the study of new
methods for acquiring, representing,
processing, and managing data within
the Intramural Research program (IRP)
clinical and research programs.
Æ Development of transactional
electronic recording and telemetry
methods for implementation in various
research environments such as clinical
neuroimaging, pharmacology and
therapeutics, and nicotine
psychopharmacology research.
Æ Development of innovative, fielddeployable tools to measure exposures
to psychosocial stress and addictive
substances within geographic contexts
in real time.
Æ Research into technology based
delivery of behavioral treatment
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interventions including contingency
management.
Despite these ongoing efforts there is a
significant need for new strategies for
leveraging advances in informatics to
advance research on drug use and
related disorders.
This Challenge welcomes bold new
ideas in these fields within the vast
scientific, clinical and technological
realms. In summary, the overarching
goal of the present Challenge is to
identify and parlay the untapped power
of other (unexpected) technologies,
fields, and innovations to inspire
transformative advances in the area of
addiction research.
Statutory Authority
This Challenge is consistent with and
advances the mission of NIDA as
described in 42 U.S.C. 285o. The general
purpose of NIDA is to conduct and
support biomedical and behavioral
research and health services research,
research training, and health
information dissemination with respect
to the prevention of drug abuse and the
treatment of drug abusers. Consistent
with this authority, one of NIDA’s
strategic goals is to support research to
improve the quality of addiction
treatment. Novel measures, conceptual
models or creative, yet feasible ideas,
and related research agendas that
achieve the goals underlying this
Challenge will help set priorities for
future research and, accordingly, will
support this strategic goal.
Rules for Participating in the Challenge
1. To be eligible to win a prize under
this Challenge, an individual or entity:
a. Shall have registered to participate
in the Challenge under the rules
promulgated by NIDA and published in
this Notice;
b. Shall have complied with all the
requirements in this Notice;
c. In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States, and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States. However,
non-U.S. citizens and non-permanent
residents can participate as a member of
a team that otherwise satisfies the
eligibility criteria. Non-U.S. citizens and
non-permanent residents are not eligible
to win a monetary prize (in whole or in
part). Their participation as part of a
winning team, if applicable, may be
recognized when the results are
announced.
d. In the case of an individual,
whether participating singly or in a
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group, must be at least 18 years old at
the time of submission;
e. May not be a Federal entity;
f. May not be a Federal employee
acting within the scope of his/her
employment, and further, in the case of
HHS employees, may not work on their
submission(s) during assigned duty
hours;
g. May not be an employee of the
National Institutes of Health (NIH), a
judge of the Challenge, or any other
party involved with the design,
production, execution, or distribution of
the Challenge or the immediate family
of such a party (i.e., spouse, parent,
step-parent, child, or step-child).
2. Federal grantees may not use
Federal funds to develop their
Challenge submissions unless use of
such funds is consistent with the
purpose of their grant award and
specifically requested to do so due to
the Challenge design.
3. Federal contractors may not use
Federal funds from a contract to develop
their Challenge submissions or to fund
efforts in support of their Challenge
submission.
4. Submissions must not infringe
upon any copyright or any other rights
of any third party. Each participant
warrants that he or she is the sole author
and owner of the work and that the
work is wholly original.
5. By participating in this Challenge,
each individual (whether competing
singly or in a group) and entity agrees
to assume any and all risks and to waive
claims against the Federal Government
and its related entities (as defined in the
COMPETES Act), except in the case of
willful misconduct, for any injury,
death, damage, or loss of property,
revenue, or profits, whether direct,
indirect, or consequential, arising from
their participation in the Challenge,
whether the injury, death, damage, or
loss arises through negligence or
otherwise.
6. Based on the subject matter of the
Challenge, the type of work that it will
possibly require, as well as an analysis
of the likelihood of any claims for death,
bodily injury, or property damage, or
loss potentially resulting from Challenge
participation, no individual (whether
competing singly or in a group) or entity
participating in the Challenge is
required to obtain liability insurance or
demonstrate financial responsibility in
order to participate in this Challenge.
7. By participating in this Challenge,
each individual (whether competing
singly or in a group) or entity agrees to
indemnify the Federal Government
against third party claims for damages
arising from or related to Challenge
activities.
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8. An individual or entity shall not be
deemed ineligible because the
individual or entity used Federal
facilities or consulted with Federal
employees during the Challenge if the
facilities and employees are made
available to all individuals and entities
participating in the Challenge on an
equitable basis.
9. Each individual (whether
competing singly or in a group) or entity
retains title and full ownership in and
to their submission and each participant
expressly reserves all intellectual
property rights (e.g., copyright) in their
submission. However, by participating
in this Challenge, each participant
grants to NIDA, and others acting on
behalf of NIDA, an irrevocable, paid-up,
royalty-free, non-exclusive, worldwide
license to use, copy for use, and display
publicly all parts of the submission for
the purposes of the Challenge. This
license may include posting or linking
to the submission on the official NIDA
Web site and making it available for use
by the public.
10. The NIH reserves the right, in its
sole discretion, to (a) cancel, suspend,
or modify the Challenge, and/or (b) not
award any prizes if no submissions are
deemed worthy.
11. Each individual (whether
competing singly or in a group) and
entity participating in this Challenge
agrees to follow applicable local, State,
and Federal laws and regulations.
12. Each individual (whether
participating singly or in a group) and
entity participating in this Challenge
must comply with all terms and
conditions of these rules, and
participation in this Challenge
constitutes each such participant’s full
and unconditional agreement to abide
by these rules. Winning is contingent
upon fulfilling all requirements herein.
Submission Requirements
Each submission for this Challenge
should consist of a white paper of no
more than 6 (double spaced) pages
describing a concept for an innovative
research initiative to advance drug
abuse and addiction research. The white
paper must include but not limited to
the following:
1. Cover page: indicate title of the
proposal and which of the following
broadly defined categories would best
describe its area of applicability:
Prevention, Behavioral treatments,
Medications development,
Epidemiology, Basic Sciences,
Neuroscience, Services and service
research, or Other (define).
2. Executive Summary (250 word
limit).
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3. A description of the innovative
concept or technology and how it was
effectively applied within another field.
4. A proposal for how the concept can
be applied to an outstanding question in
drug abuse/addiction research,
including a discussion of why that
question is important to address.
5. A cogent rationale for why the
proposed concept would work in the
field of drug use and addiction research.
The white paper must not contain any
information directly identifying the
participants.
To register for this Challenge,
participants must go to
www.challenge.gov and search for
‘‘Harnessing insights from other
disciplines to advance drug abuse and
addiction research.’’ Click on the title to
go to the Challenge platform Web site,
which contains instructions on how to
register and submit.
All submissions must be in English.
Each submission must consist of a PDF
file, containing the white paper
document. The PDF documents must be
formatted to be no larger than 8.5’’ by
11.0’’, with at least 1 inch margins and
can include a maximum of two figures.
The white paper must be no more than
6 pages long. Font size must be no
smaller than 11 point Arial. The
participant must not use HHS’s logo or
official seal or the logo of NIH or NIDA
in the submission, and must not claim
federal government endorsement.
Amount of the Prize
Up to three monetary prizes may be
awarded: $15,000 for 1st Place, $7,000
for 2nd Place, $3,000 for 3rd Place for
a total prize award pool of up to
$25,000. The names of the winners and
the titles of their submissions will be
posted on the NIDA Web site. The
award approving official for this
Challenge is the Director of the National
Institute on Drug Abuse.
Payment of the Prize
Prizes awarded under this Challenge
will be paid by electronic funds transfer
and may be subject to Federal income
taxes. The NIH will comply with the
Internal Revenue Service withholding
and reporting requirements, where
applicable.
Basis Upon Which Winner Will Be
Selected
The judging panel will make
recommendations to the Award
Approving Official based upon the
following three criteria and point
allocation:
1. Novelty of the concept (5 points):
Concepts shall move the field beyond
the existing paradigms commonly used
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in addiction research, and focus on
novel, underserved, neglected, complex,
or intractable aspects of the addiction
phenomenon. How novel is the
concept? Does it address important
basic or clinical features/effects that are
not currently or adequately addressed
and/or with a fresh perspective?
2. Feasibility (5 points): Ideas,
concepts and the approaches, measures
and systems derived from them must be
rooted on a rational, scientific or
otherwise cogent background that
would guarantee a modicum of
feasibility given the current challenges
and state of the art in the field of
addiction. How well does the research
agenda describe the gaps in the relevant
areas of science that need to be
addressed by this new approach/
concept to be achieved and
implemented? Does the agenda describe
a logical, feasible plan and timeframe
for addressing those gaps?
3. Importance of the question being
addressed/likelihood of impact (5
points): How effective would the
successful completion of the project be
in addressing addiction, enhancing
prevention, or improving clinical
outcomes? How well does it consider
factors relevant to the ultimate success
of the concept? How well does it
harness innovations from other fields to
the existing addiction knowledge base
toward advancing drug abuse and
addiction research?
Scores from each criterion will be
weighted equally. The score for each
submission will be the sum of the scores
from each of the 5 voting judges, for a
maximum of 75 points. NIDA reserves
the right to make an award to
submissions scoring less than 75 points
if NIDA deems any sufficiently
meritorious. All submissions will be
held until after the deadline is reached
for a simultaneous judging process.
NIDA reserves the right to disqualify
and remove any submission that is
deemed, in NIDA’s or the judging
panel’s discretion, inappropriate,
offensive, defamatory, or demeaning.
NIDA reserves the right not to award
any prizes in case none is found to be
sufficiently meritorious.
The evaluation process will begin by
anonymizing and removing those that
are not responsive to this Challenge or
not in compliance with all of the rules
of eligibility. Submissions that are
responsive and in compliance will
undergo a preliminary review by the
Challenge Judges with expertise in the
relevant areas of science Challenge
Judges will examine all responsive and
compliant submissions, as well
comments from program staff, if any,
and score the submissions in
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accordance with the judging criteria
outlined above. Judges will meet to
discuss the most meritorious
submissions. Final recommendations
will be determined by electronic
(majority) vote of the judges.
Challenge Judges
Dr. Nora Volkow, Director, National
Institute on Drug Abuse (NIDA)—Ex
Officio
Dr. Roger Little, Deputy Director,
Division of Basic Neuroscience and
Behavioral Research, NIDA
Dr. David Epstein, Associate Scientist,
Intramural Research Program, NIDA
Dr. David Liu, Team Leader, Medical
Officer, Center for Clinical Trials
Network, NIDA
Dr. Maureen Boyle, Chief, Science
Policy Branch, Office of Science
Policy and Communication, NIDA
Dr. Meyer D. Glantz, Associate Director
for Science, Division of Epidemiology,
Services, and Prevention Research
Dr. Ruben Baler, Health Scientist
Administrator, Science Policy Branch,
Office of Science Policy and
Communication, NIDA
Dr. Steve Grant, Chief, Clinical
Neuroscience Branch, Division of
Clinical Neuroscience and Behavioral
Research, NIDA
Dr. Philip Krieter, Pharmacologist,
Division of Pharmacotherapies and
Medical Consequences of Drug Abuse,
NIDA
Dr. Gerald McLaughlin, Chief, Scientific
Review Branch, Division of
Extramural Research, NIDA
Dated: May 11, 2015.
Nora D. Volkow,
Director, National Institute on Drug Abuse,
National Institutes of Health.
[FR Doc. 2015–12632 Filed 5–22–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; 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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individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Heart, Lung, and
Blood Initial Review Group; NHLBI
Mentored Transition to Independence
Review Committee.
Date: June 11–12, 2015.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: The William F. Bolger Center, 9600
Newbridge Drive, Potomac, MD 20854.
Contact Person: Giuseppe Pintucci, Ph.D.
Scientific Review Officer, Office of Scientific
Review/DERA National Heart, Lung, and
Blood Institute, 6701 Rockledge Drive, Room
7192, , Bethesda, MD 20892, 301–435–0287,
Pintuccig@nhlbi.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: May 19, 2015.
Carolyn Baum,
Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–12538 Filed 5–22–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Amended
Notice of Meeting
Notice is hereby given of a change in
the meeting of the Systemic Injury by
Environmental Exposure, June 17, 2015,
08:00 a.m. to June 18, 2015, 05:00 p.m.,
Hyatt Regency Bethesda, One Bethesda
Metro Center, 7400 Wisconsin Avenue,
Bethesda, MD, 20814 which was
published in the Federal Register on
May 13, 2015, 80 FR Pg. 28630.
The meeting will be held on 06/18/
2015–06/19/2015 instead of 06/17/
2015–06/18/2015. The meeting time and
location remains the same. The meeting
is closed to the public.
Dated: May 19, 2015.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–12545 Filed 5–22–15; 8:45 am]
BILLING CODE 4140–01–P
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[Federal Register Volume 80, Number 100 (Tuesday, May 26, 2015)]
[Notices]
[Pages 30084-30087]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-12632]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Announcement of Requirements and Registration for: ``Harnessing
Insights From Other Disciplines To Advance Drug Abuse and Addiction
Research'' Challenge
Authority: 15 U.S.C. 3719.
SUMMARY: The National Institute on Drug Abuse (NIDA), a component of
the National Institutes of Health (NIH), is seeking from the general
public ideas on how to adapt specialized knowledge from other
disciplines to inform new directions and discoveries in drug abuse and
addiction research. With the ``Harnessing insights from other
disciplines to advance drug abuse and addiction research'' challenge
(the ``Challenge''), NIDA aims to gain insights into new methods or
approaches that could transform discovery in order to significantly
expand our basic knowledge about drug abuse and addiction processes,
accelerate the development of novel and more effective prevention and
treatment strategies, and/or enhance our capacity to implement,
monitor, and improve upon evidence-based interventions.
This Challenge is soliciting written proposals that outline novel
approaches to addressing research challenges in the drug use and
addiction field by leveraging concepts or technologies from other
disciplines. This Challenge is being issued as part of NIDA's strategic
planning process for 2016-2020. Winning proposals may be used to guide
the development of new research programs within NIDA.
DATES:
(1) Submission Period begins May 26, 2015, 9:00 a.m., EST
(2) Submission Period ends June 22, 2015, 11:59 p.m., EST
(3) Judging Period June 23, 2015 to July 17, 2015
(4) Winners Announced July 30, 2015
FOR FURTHER INFORMATION CONTACT: Dr. Emily Einstein, Ph.D., Science
Policy Branch, Office of Science Policy and Communication, National
Institute on Drug Abuse, Phone: 301-443-6071, Email:
emily.einstein@nih.gov.
SUPPLEMENTARY INFORMATION:
Subject of the Challenge
For the past four decades, the National Institute on Drug Abuse
(NIDA) has led the way in supporting research to prevent and treat drug
abuse and addiction and to mitigate the impact of their consequences,
which include the spread of HIV/AIDS and other infectious diseases. To
confront the most pressing aspects of the complex disease of addiction
and to tackle its underlying causes, NIDA's strategic approach is
multipronged and includes research programs in basic, clinical, and
translational sciences. These programs support studies in genetics,
functional neuroimaging, social neuroscience, medication and behavioral
therapies, prevention, and health services, including cost-
effectiveness research. NIDA's evolving portfolio has produced a vast
body of knowledge that informs strategic directions for future
research, and this Challenge represents a new approach to broaden the
pool of testable ideas.
Scientific knowledge about drug addiction and its treatment has
increased markedly over the past couple of decades. Today, we have a
better understanding of the effects of drugs on the brain, as well as
new and more effective treatments than were available in the past. A
changing healthcare landscape may provide opportunities to further
enhance the quality of addiction prevention and treatment. Still,
addiction remains a pressing public health issue, and this Challenge
seeks to accelerate progress in the field of drug abuse and addiction
research by incentivizing a broader community of stakeholders--
including those not formally involved in biomedical or addiction-
related disciplines--to propose new ideas or innovations that leverage
concepts or technologies from other disciplines to advance drug abuse
and addiction research.
While preparing their proposals, applicants should bear in mind
NIDA's traditional priority areas, persistent roadblocks that hamper
progress, and evolving and emerging opportunities. Some illustrative
examples are discussed below; however, proposals may address any
challenge within the drug use and addiction field.
NIDA priority areas. NIDA's charge, to bring the power of science
to bear on drug abuse and addiction, has two critical components. The
first is the strategic support and conduct of research across a broad
range of disciplines. The second is ensuring the rapid and effective
dissemination and implementation of the results of that research to
significantly improve
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prevention and treatment and to inform policy as it relates to drug use
and addiction. These aims are currently met by a broad range of
projects in basic, clinical, and translational sciences. For more
information on current NIDA research programs please visit
www.drugabuse.gov.
Roadblocks to progress in addiction research and its translation.
There are many scientific and non-scientific roadblocks that hamper
progress on drug use and addiction research. For example, one of the
most frequently cited obstacles to clinical advances in the field of
drug use disorders is the lack of interest by the pharmaceutical
industry in developing new addiction medications. This is largely due
to the low success rate of clinical trials for neurotherapeutics and
the perceived lack of financial incentives to pursue new
pharmacotherapies for substance use disorders. Other key obstacles
include the reluctance of some primary care providers to address
substance abuse with their patients. On the basic research side,
reproducibility, transparency, data sharing, and training a diverse
workforce remain areas in need of improvement.
Emerging Opportunities. New discoveries, technologies, paradigms,
and ways of thinking play a key role in our efforts to understand
addiction, to develop better ways to influence addiction trajectories,
and to mitigate its consequences. The examples below are meant to
illustrate just a few areas of rapidly evolving technologies and
emerging opportunities from which the drug use and addiction field
expects to reap significant benefits in the near future.
Genomics and Epigenomics. Recent technological developments have
led to important advances in linking genes and their regulation with
behavior. We now have an unprecedented capacity to screen for thousands
of genetic and epigenetic variations and catalogue how they modulate
substance use disorder risk by influencing gene expression, brain
maturation, neural architecture, and behavioral patterns. In addition,
advances in epigenetics research are enabling increased understanding
of how environmental factors (e.g., parenting style, drug exposure) can
affect the expression of specific genes to either strengthen or weaken
risk for substance use and addiction. Similar approaches could be
applied to leverage advances in metabolomics, proteomics, connectomes,
transcriptomics and systems biology to better characterize the role of
these systems in drug use and addiction.
Big Data. Behavioral disorders including drug use disorders are
incredibly complex, with multiple biological, environmental, and
developmental factors contributing to risk. Very large data sets (on
the scale of tera- or petabytes, typically referred to as ``Big Data'')
sets are essential platforms for the analysis of such complex systems,
overlaying genetic, molecular, cellular, environmental, behavioral, and
structural and functional brain imaging data. Big Data also brings
analysis opportunities in many other areas, such as social media and
socio-economic mapping which, when combined with health information,
could lead to an improved understanding of predictors of psychiatric
illness risk (including addiction), trajectory, and treatment
responses. This area of development presents significant opportunities
for innovation for research.
Data Sharing. Data sharing is a critical component that allows the
results of NIDA's research to be distributed to investigators and the
public in order to promote new research, encourage further analyses,
and disseminate information to the community. Secondary analyses of
shared data multiply the scientific contribution of the original
research. The development of new strategies to facilitate effective
data sharing and analysis is one area in which new ideas could spur
significant advancement.
Informatics. NIDA is already pursuing several avenues to realize
the research and clinical potential of various informatics tools.
Notable examples include:
[cir] Development of a comprehensive clinical decision support
systems based on advanced database analysis techniques.
[cir] Research in theoretical and applied areas of medical and
clinical informatics, including the study of new methods for acquiring,
representing, processing, and managing data within the Intramural
Research program (IRP) clinical and research programs.
[cir] Development of transactional electronic recording and
telemetry methods for implementation in various research environments
such as clinical neuroimaging, pharmacology and therapeutics, and
nicotine psychopharmacology research.
[cir] Development of innovative, field-deployable tools to measure
exposures to psychosocial stress and addictive substances within
geographic contexts in real time.
[cir] Research into technology based delivery of behavioral
treatment interventions including contingency management.
Despite these ongoing efforts there is a significant need for new
strategies for leveraging advances in informatics to advance research
on drug use and related disorders.
This Challenge welcomes bold new ideas in these fields within the
vast scientific, clinical and technological realms. In summary, the
overarching goal of the present Challenge is to identify and parlay the
untapped power of other (unexpected) technologies, fields, and
innovations to inspire transformative advances in the area of addiction
research.
Statutory Authority
This Challenge is consistent with and advances the mission of NIDA
as described in 42 U.S.C. 285o. The general purpose of NIDA is to
conduct and support biomedical and behavioral research and health
services research, research training, and health information
dissemination with respect to the prevention of drug abuse and the
treatment of drug abusers. Consistent with this authority, one of
NIDA's strategic goals is to support research to improve the quality of
addiction treatment. Novel measures, conceptual models or creative, yet
feasible ideas, and related research agendas that achieve the goals
underlying this Challenge will help set priorities for future research
and, accordingly, will support this strategic goal.
Rules for Participating in the Challenge
1. To be eligible to win a prize under this Challenge, an
individual or entity:
a. Shall have registered to participate in the Challenge under the
rules promulgated by NIDA and published in this Notice;
b. Shall have complied with all the requirements in this Notice;
c. In the case of a private entity, shall be incorporated in and
maintain a primary place of business in the United States, and in the
case of an individual, whether participating singly or in a group,
shall be a citizen or permanent resident of the United States. However,
non-U.S. citizens and non-permanent residents can participate as a
member of a team that otherwise satisfies the eligibility criteria.
Non-U.S. citizens and non-permanent residents are not eligible to win a
monetary prize (in whole or in part). Their participation as part of a
winning team, if applicable, may be recognized when the results are
announced.
d. In the case of an individual, whether participating singly or in
a
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group, must be at least 18 years old at the time of submission;
e. May not be a Federal entity;
f. May not be a Federal employee acting within the scope of his/her
employment, and further, in the case of HHS employees, may not work on
their submission(s) during assigned duty hours;
g. May not be an employee of the National Institutes of Health
(NIH), a judge of the Challenge, or any other party involved with the
design, production, execution, or distribution of the Challenge or the
immediate family of such a party (i.e., spouse, parent, step-parent,
child, or step-child).
2. Federal grantees may not use Federal funds to develop their
Challenge submissions unless use of such funds is consistent with the
purpose of their grant award and specifically requested to do so due to
the Challenge design.
3. Federal contractors may not use Federal funds from a contract to
develop their Challenge submissions or to fund efforts in support of
their Challenge submission.
4. Submissions must not infringe upon any copyright or any other
rights of any third party. Each participant warrants that he or she is
the sole author and owner of the work and that the work is wholly
original.
5. By participating in this Challenge, each individual (whether
competing singly or in a group) and entity agrees to assume any and all
risks and to waive claims against the Federal Government and its
related entities (as defined in the COMPETES Act), except in the case
of willful misconduct, for any injury, death, damage, or loss of
property, revenue, or profits, whether direct, indirect, or
consequential, arising from their participation in the Challenge,
whether the injury, death, damage, or loss arises through negligence or
otherwise.
6. Based on the subject matter of the Challenge, the type of work
that it will possibly require, as well as an analysis of the likelihood
of any claims for death, bodily injury, or property damage, or loss
potentially resulting from Challenge participation, no individual
(whether competing singly or in a group) or entity participating in the
Challenge is required to obtain liability insurance or demonstrate
financial responsibility in order to participate in this Challenge.
7. By participating in this Challenge, each individual (whether
competing singly or in a group) or entity agrees to indemnify the
Federal Government against third party claims for damages arising from
or related to Challenge activities.
8. An individual or entity shall not be deemed ineligible because
the individual or entity used Federal facilities or consulted with
Federal employees during the Challenge if the facilities and employees
are made available to all individuals and entities participating in the
Challenge on an equitable basis.
9. Each individual (whether competing singly or in a group) or
entity retains title and full ownership in and to their submission and
each participant expressly reserves all intellectual property rights
(e.g., copyright) in their submission. However, by participating in
this Challenge, each participant grants to NIDA, and others acting on
behalf of NIDA, an irrevocable, paid-up, royalty-free, non-exclusive,
worldwide license to use, copy for use, and display publicly all parts
of the submission for the purposes of the Challenge. This license may
include posting or linking to the submission on the official NIDA Web
site and making it available for use by the public.
10. The NIH reserves the right, in its sole discretion, to (a)
cancel, suspend, or modify the Challenge, and/or (b) not award any
prizes if no submissions are deemed worthy.
11. Each individual (whether competing singly or in a group) and
entity participating in this Challenge agrees to follow applicable
local, State, and Federal laws and regulations.
12. Each individual (whether participating singly or in a group)
and entity participating in this Challenge must comply with all terms
and conditions of these rules, and participation in this Challenge
constitutes each such participant's full and unconditional agreement to
abide by these rules. Winning is contingent upon fulfilling all
requirements herein.
Submission Requirements
Each submission for this Challenge should consist of a white paper
of no more than 6 (double spaced) pages describing a concept for an
innovative research initiative to advance drug abuse and addiction
research. The white paper must include but not limited to the
following:
1. Cover page: indicate title of the proposal and which of the
following broadly defined categories would best describe its area of
applicability: Prevention, Behavioral treatments, Medications
development, Epidemiology, Basic Sciences, Neuroscience, Services and
service research, or Other (define).
2. Executive Summary (250 word limit).
3. A description of the innovative concept or technology and how it
was effectively applied within another field.
4. A proposal for how the concept can be applied to an outstanding
question in drug abuse/addiction research, including a discussion of
why that question is important to address.
5. A cogent rationale for why the proposed concept would work in
the field of drug use and addiction research.
The white paper must not contain any information directly
identifying the participants.
To register for this Challenge, participants must go to
www.challenge.gov and search for ``Harnessing insights from other
disciplines to advance drug abuse and addiction research.'' Click on
the title to go to the Challenge platform Web site, which contains
instructions on how to register and submit.
All submissions must be in English. Each submission must consist of
a PDF file, containing the white paper document. The PDF documents must
be formatted to be no larger than 8.5'' by 11.0'', with at least 1 inch
margins and can include a maximum of two figures. The white paper must
be no more than 6 pages long. Font size must be no smaller than 11
point Arial. The participant must not use HHS's logo or official seal
or the logo of NIH or NIDA in the submission, and must not claim
federal government endorsement.
Amount of the Prize
Up to three monetary prizes may be awarded: $15,000 for 1st Place,
$7,000 for 2nd Place, $3,000 for 3rd Place for a total prize award pool
of up to $25,000. The names of the winners and the titles of their
submissions will be posted on the NIDA Web site. The award approving
official for this Challenge is the Director of the National Institute
on Drug Abuse.
Payment of the Prize
Prizes awarded under this Challenge will be paid by electronic
funds transfer and may be subject to Federal income taxes. The NIH will
comply with the Internal Revenue Service withholding and reporting
requirements, where applicable.
Basis Upon Which Winner Will Be Selected
The judging panel will make recommendations to the Award Approving
Official based upon the following three criteria and point allocation:
1. Novelty of the concept (5 points): Concepts shall move the field
beyond the existing paradigms commonly used
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in addiction research, and focus on novel, underserved, neglected,
complex, or intractable aspects of the addiction phenomenon. How novel
is the concept? Does it address important basic or clinical features/
effects that are not currently or adequately addressed and/or with a
fresh perspective?
2. Feasibility (5 points): Ideas, concepts and the approaches,
measures and systems derived from them must be rooted on a rational,
scientific or otherwise cogent background that would guarantee a
modicum of feasibility given the current challenges and state of the
art in the field of addiction. How well does the research agenda
describe the gaps in the relevant areas of science that need to be
addressed by this new approach/concept to be achieved and implemented?
Does the agenda describe a logical, feasible plan and timeframe for
addressing those gaps?
3. Importance of the question being addressed/likelihood of impact
(5 points): How effective would the successful completion of the
project be in addressing addiction, enhancing prevention, or improving
clinical outcomes? How well does it consider factors relevant to the
ultimate success of the concept? How well does it harness innovations
from other fields to the existing addiction knowledge base toward
advancing drug abuse and addiction research?
Scores from each criterion will be weighted equally. The score for
each submission will be the sum of the scores from each of the 5 voting
judges, for a maximum of 75 points. NIDA reserves the right to make an
award to submissions scoring less than 75 points if NIDA deems any
sufficiently meritorious. All submissions will be held until after the
deadline is reached for a simultaneous judging process. NIDA reserves
the right to disqualify and remove any submission that is deemed, in
NIDA's or the judging panel's discretion, inappropriate, offensive,
defamatory, or demeaning. NIDA reserves the right not to award any
prizes in case none is found to be sufficiently meritorious.
The evaluation process will begin by anonymizing and removing those
that are not responsive to this Challenge or not in compliance with all
of the rules of eligibility. Submissions that are responsive and in
compliance will undergo a preliminary review by the Challenge Judges
with expertise in the relevant areas of science Challenge Judges will
examine all responsive and compliant submissions, as well comments from
program staff, if any, and score the submissions in accordance with the
judging criteria outlined above. Judges will meet to discuss the most
meritorious submissions. Final recommendations will be determined by
electronic (majority) vote of the judges.
Challenge Judges
Dr. Nora Volkow, Director, National Institute on Drug Abuse (NIDA)--Ex
Officio
Dr. Roger Little, Deputy Director, Division of Basic Neuroscience and
Behavioral Research, NIDA
Dr. David Epstein, Associate Scientist, Intramural Research Program,
NIDA
Dr. David Liu, Team Leader, Medical Officer, Center for Clinical Trials
Network, NIDA
Dr. Maureen Boyle, Chief, Science Policy Branch, Office of Science
Policy and Communication, NIDA
Dr. Meyer D. Glantz, Associate Director for Science, Division of
Epidemiology, Services, and Prevention Research
Dr. Ruben Baler, Health Scientist Administrator, Science Policy Branch,
Office of Science Policy and Communication, NIDA
Dr. Steve Grant, Chief, Clinical Neuroscience Branch, Division of
Clinical Neuroscience and Behavioral Research, NIDA
Dr. Philip Krieter, Pharmacologist, Division of Pharmacotherapies and
Medical Consequences of Drug Abuse, NIDA
Dr. Gerald McLaughlin, Chief, Scientific Review Branch, Division of
Extramural Research, NIDA
Dated: May 11, 2015.
Nora D. Volkow,
Director, National Institute on Drug Abuse, National Institutes of
Health.
[FR Doc. 2015-12632 Filed 5-22-15; 8:45 am]
BILLING CODE 4140-01-P