Release Date:  August 25, 1998



National Institute of Mental Health

This Request For Information (RFI)/Sources Sought Notice (SS) is for information
and planning purposes only and shall not be construed as a solicitation or as an
obligation on the part of the National Institute of Mental Health (NIMH).  The
purpose of this RFI/SS is to identify potential sources that may be interested
in and capable of performing the work described herein.  NIMH welcomes comments
from all individuals on each or all of these questions.  The NIMH does not intend
to award a contract on the basis of responses nor otherwise pay for the
preparation of any information submitted or NIMHþs  use of such information.  
Acknowledgment of receipt of responses will not be made, nor will respondents be
notified of the NIMH's evaluation of the information received.  As a result of
this RFI/SS, the NIMH may issue a Request for Proposals (RFP).  In the event a
RFP will be issued, Standard Industrial Classification (SIC) code 8093 will
apply.  However, should such a requirement materialize, no basis for claims
against the NIMH shall arise as a result of a response to this RFI or the NIMH's
use of such information as either part of our evaluation process or in developing
specifications for any subsequent requirement. 

Request for Information: 

The NIMH seeks input and comment on its plans to study the comparative efficacy
and effectiveness of the new atypical antipsychotics.  NIMH intends to award a
single contract with multiple scientific and administrative components to conduct
trials of these drugs in patients with schizophrenia, patients with psychotic
depression, and patients with dementia.  NIMH expects to fund three,
scientifically independent treatment trials along with a shared
administrative/logistical core.  NIMH anticipates and strongly encourages
collaboration between multiple research centers and between academic institutions
and private businesses in submitting proposals.  An offeror may participate in
multiple proposals as subcontractor, coinvestigator, or offeror, and may be the
Principal Investigator (PI) on a subcontract in more than one proposal.  However,
an offeror may be overall PI or primary contractor on only one proposal.  The
overriding concern is the technical merit and scientific quality of the
individual trials, and NIMH reserves the right to eliminate one or even two
trials from a proposal if they are deemed insufficiently meritorious.

The trials will be based on a public health model of interventions research, with
a focus on effectiveness and outcome, rather than efficacy alone.  They will also
examine cost-effectiveness and the impact of external factors on treatment
delivery, compliance, and eventual outcome.  A major objective is
generalizability: the trials will be as inclusive as possible; a premium will be
placed on demographic (age, sex, and race) and geographic (urban and rural)
diversity; and multiple treatment and residential settings will be included. 
Subjects with comorbid disorders (e.g., drug abuse) will not be excluded, and
will be actively recruited. Only FDA approved, marketed antipsychotics will be
studied.  One of the anticipated results of the present initiative is the
development of a network of sites and investigators able to respond to future
needs for outcome focused treatment research.

At this time NIMH is considering the following aims and hypotheses for each
trial:  In schizophrenia, the overriding issue will be how these drugs affect
long-term outcome: not only positive and negative symptoms, but overall level of
function in multiple domains including cognition, mood, suicidality,
interpersonal interactions, vocational achievement, and quality of life.  In
psychotic depression, the objectives are to determine the relative risks and
benefits of chronic, prophylactic treatment with the atypicals.  In patients with
dementia, the questions have to do with acute efficacy and safety: defining which
symptoms and behaviors are appropriately treated with the new antipsychotics,
unique safety issues, and effects on long-term outcome.

To aid in the design of a possible future solicitation, we as that interested
organizations submit comments on the following issues: 
1) Are the specific aims stated above for each diagnosis (trial) the most
important objectives for an NIMH sponsored trial of the new atypical
antipsychotics?  Are there other questions that are more compelling, and if so,
what are they?

2) How needed are acute efficacy studies in psychotic depression and Alzheimer's
Disease, and is this more urgent than long-term outcome data. 

3) For each trial (schizophrenia, psychotic depression, and dementia),
approximately how many subjects will be needed (assuming that a 10% difference
in outcome is the minimum non-trivial effect) in order to reach acceptable power? 
How long a trial is needed?

4) How might non-pharmacological (psychosocial) interventions be handled so that
interactive effects with the new antipsychotics can be accounted for (short of
a randomized trial of combined psychosocial/psychopharmacological intervention)?

5) What are the appropriate control, "standard" treatments for each trial,
keeping in mind the balance between the need for scientific rigor with ethical
treatment of subjects.

6) How might practitioners at sites not previously involved in
psychopharmacological trials, particularly those in the managed care or public
setting, be involved in these trials?

7) How might the trials be more inclusive - minimizing exclusion criteria and
maximizing subject retention.

NIMH welcomes responses from all individuals and organizations on each or all of
these questions.  Responses should be limited to approximately one (1) page per
question, and are due by September 9, 1998.  

Sources Sought: 

Interest organizations should submit a capability statement of approximately 10
pages that details the ability to perform the aspects of the effort described
above. All proprietary information should be marked as such. Responses will be
reviewed only by NIH personnel and will be held in a confidential manner. 

All respondents are asked to indicate the type and size of your business
organization, e.g., Large Business, Small Business, Small Disadvantaged Business,
Women-Owned Business, 8(a), Historically Black College or University/Minority
Institution (HBCU/MI), educational institution, profit/non-profit hospital, or
other nonprofit organization, in their response.  

Responses should be identified with NIMH-98-RFI-01, and are due by September 9,
1998.  Please submit three (3) copies of your response to the attention of:
Patricia L. Gibbons, Contracting Officer, at address shown below.  Facsimile
responses will also be accepted as long as they do not exceed 20 pages in length.
E-mail responses will also be accepted.


Inquiries concerning this Notice may be directed to:

Patricia L. Gibbons
Contracts Management Branch
National Institute of Mental Health
5600 Fishers Lane, Room 9C-15
Rockville, MD  20857-8030
Telephone:  (301) 443-2696
FAX:  (301) 443-0501

Return to Volume Index

Return to NIH Guide Main Index

Office of Extramural Research (OER) - Home Page Office of Extramural
Research (OER)
  National Institutes of Health (NIH) - Home Page National Institutes of Health (NIH)
9000 Rockville Pike
Bethesda, Maryland 20892
  Department of Health and Human Services (HHS) - Home Page Department of Health
and Human Services (HHS) - Government Made Easy

Note: For help accessing PDF, RTF, MS Word, Excel, PowerPoint, Audio or Video files, see Help Downloading Files.