MEETINGS & PRESENTATIONS

Over the two-year project period, there will be six consensus-oriented meetings held in the Washington, D.C. area. The dates and registration information for the meetings will be available through this website.

A published workshop report or summary will follow each meeting that disseminates the results.

2003 2004 2005
Conference 1 - completed Conference 4 - completed MATRICS Presentations at ICOSR
Conference 2 - completed Conference 5 - completed  
Conference 3 - completed Conference 6, September 9-10  

2003

2004

2005

  • Matrics Presentations at the International Congress on Schizophrenia Research, April 2005

    Presentations

CONFERENCE 1

Identifying Cognitive Targets and Establishing Criteria for Test Selection

Conference Chair: Michael F. Green, Ph.D.

Dates and Registration
Held April 14 - 15 at the Bolger Center in Potomac, MD.
Agenda & Slides
 
April 14th, 2003
The first day will include a welcome from Tom Insel, Director of NIMH, and an overview of the MATRICS Program. Starting after lunch, there will be a series of presentations on cognitive topics that will be followed by ample periods of discussion and participation by the invited experts. The first meeting will also include discussion with the representatives from the FDA focused on understanding their perspective on issues related to measurement selection.
April 15th, 2003
The presentations will continue on the morning of the second day until around 11AM. When the presentations conclude, the Neurocognition Committee will meet to review and discuss the information presented. This information will be used to help guide decisions regarding (a) the cognitive targets for pharmacological intervention, and (b) the most desirable criteria for selection of a neurocognitive battery. A later consensus meeting will be held to evaluate candidate cognitive batteries and to select a consensus battery. Decisions will be reached at the first meeting regarding a standard format for evaluation of candidate batteries submitted for consideration at conference #3.
Goals of Conference
  1. To develop a consensus among a diverse group of academic and industry scientists as to what is known about the types and magnitudes of cognitive deficits in schizophrenia. Emphasis will be given to identifying deficits that contribute uniquely to individual heterogeneity in cognitive deficits within schizophrenia.
  2. To develop a consensus among a diverse group of academic and industry scientists as to the most fruitful cognitive targets for pharmacological intervention in schizophrenia. Emphasis will be given to those deficits linked to functional outcome.
  3. To develop a consensus among a diverse group of academic and industry scientists as to the most desirable criteria to use for selection of cognitive tests.
Process
The goals of the first conference will be achieved by using a consensus building approach. Prior to the meeting, approximately 70 “experts” will be invited to participate in a phone interview. The experts will represent the following areas:
  • clinical trials methodology
  • cognitive neuroscience
  • cognitive science
  • neuropharmacology
  • psychometrics/test development
  • outcome assessment
  • biostatistics

The interview will include open-ended questions about issues critical to the selection of a neurocognitive test battery to assess cognitive changes in schizophrenia. Areas to be covered within the interview include questions about:

  • reliability
  • predictive validity for functional outcome
  • required training for test administrators
  • importance of normative data and test interpretation
  • coverage of cognitive domains
  • duration of the test battery
  • relative importance of test qualities
  • types of outcome assessment
  • nomination of opinion leaders

Participants will also be asked to rate the importance of test criteria within selected areas. A summary of the responses obtained from the interviews will be shared with members of the MATRICS Neurocognition Committee, but not in a way that identifies the individual respondents.

The results from the two-day meeting will be summarized in a special article to be published in a journal agreed upon by NIMH and the Neurocognition Committee. The article will briefly review the content of the presentations and will concentrate on a summary of the facilitated discussions and the recommendations of the group. If there are conflicting points of view, these will be reflected in the manuscript. The manuscript will be reviewed by all members of the Neurocognition Committee for accuracy and completeness prior to submission for publication.


Conference #2

Neuropsychopharmacological approaches to modulating cognition in schizophrenia: Approaches to identifying promising compounds

Conference Co-Chairs: Carol Tamminga, M.D. & Mark Geyer, Ph.D.

Dates and Registration
June 23 - 24, 2003 at the National Institute of Health (NIH) campus
Building 31 in Bethesda, MD.
National Institutes of Health Building 31, 6th floor
9000 Rockville Pike
Bethesda, MD 20892
Conference Room # 10
Phone (301) 496-9966
Information and Registration Materials
Agenda, Slides and Transcripts
Goals of Conference
  1. To develop a consensus among a diverse group of academic and industry scientists as to the most promising neural system targets for improving cognition in schizophrenia.
  2. To develop a consensus among the same group of scientists as to the most promising models for use in drug development in the area of cognition in schizophrenia. This will include animal models – including non-human primate models – and human models.
  3. To develop a consensus among the same group of scientists regarding the most promising available compounds for study in the immediate future. This will be separated into compounds that may be incorporated into controlled and pilot trials in humans as well as compounds that should be studied through animal models.
June 23, 2003
The first day will include a welcome from Ellen Stover, Director, NIMH Division of Mental Disorders, Behavioral Research, and AIDS, and an overview of the MATRICS Program provided by Wayne Fenton, M.D. (NIMH Project Officer) and Steve Marder, M.D. (MATRICS P.I.). MATRICS updates for the Neurocognition and Government/Industry Committees will be provided by Michael Green, Ph.D., Keith Nuechterlein, Ph.D., and Dan Bush, Ph.D. The morning session will conclude with a summary of the findings from the Neuropharmacology interview, presented by Robert Buchanan, M.D. After lunch, there will be a series of presentations on neuropharmacological topics that will be followed by ample discussion time for the conference attendees.
June 24, 2003
The presentations will continue on the second day until 5 PM. When the presentations conclude, the Neuropharmacology Committee will meet to review and discuss the opinions expressed and information learned from the meeting. This information will be used to help guide decisions regarding the most promising neuropharmacological targets, animal and human models for use in drug development, and available compounds, as well as the methods used to evaluate them. The RAND Panel meeting to be held in September will be used to evaluate the most promising candidates. A decision will be reached at the first meeting regarding a standard format for evaluation of candidate targets submitted for consideration.
Process
Similar to conference #1, the goals will be achieved by using a consensus building approach. Prior to the meeting, approximately 60 "experts" will be invited to participate in a phone interview. The experts will represent the following areas:

  • Cognitive Neuroscience (examination of neural systems underlying cognitive deficits or underlying schizophrenia)
  • Cognitive Science (measurement of cognitive processes in normal individuals or in other disorders)
  • Neuropharmacology in Animals
  • Neuropharmacology in Humans

The interview includes open-ended questions and ratings. Areas to be covered include:

  • Pharmacological and methodological issues
  • Identification of receptor or molecular targets of interest
  • Criteria to be considered for evaluating potential targets and agents
  • Issues concerning the phenomenology of cognitive dysfunction in schizophrenia

A summary of the responses obtained from the interviews will be shared with members of the MATRICS Neuropharmacology Committee, but not in a way that identifies the individual respondents. The results from the two-day meeting will be summarized in a special article, or series of articles, to be published in a journal agreed upon by NIMH and the Neuropharmacology Committee. The article(s) will briefly review the content of the presentations and will concentrate on a summary of the facilitated discussions and the recommendations of the group. If there are conflicting points of view, these will be reflected in the manuscript.


Conference #3

RAND Panels for Evaluation of Candidate Neurocognitive Tests

Conference Chairs

Neurocognition Panel: Keith H. Nuechterlein, Ph.D. (Chair) and Michael F. Green, Ph.D. (Co-chair)

Dates and Registration
September 29, 2003
Registration by invitation only.
Materials used by the RAND Panel to arrive at its ratings of each criterion of the candidate neurocognition tests.

Results of the MATRICS RAND Panel Meeting:
Average Medians for the Categories of Each Candidate Test

Psychometric Validation Study - Cognitive Battery, beta version

MATRICS Consensus Cognitive Battery for Clinical Trials, Beta Version

Goals of Conference
Neurocognition
  1. To evaluate various cognitive tests and batteries according to the criteria that were prioritized in the first consensus conference. The first part of the evaluations will occur by the panelists prior to the meeting. The final phase of evaluations will occur at the consensus meeting.
  2. To arrive at a recommendation for a core cognitive battery based on the evaluations of the panelists. The RAND Panel Method will be used to facilitate agreement.
Process
The Neurocognition goals will be achieved by using a modification of the RAND/UCLA Panel Method. The objective of the RAND/UCLA Panel Method is to enhance agreement among experts in making decisions based on incomplete databases. The process is an iterative one in which experts initially provide anonymous ratings on selected questions or criteria prior to a face-to-face meeting with other experts who have rated the same items. At the conference, each member of the panel sees their ratings vis-à-vis those of the other panelists. After discussion, all panelists re-rate the same questions.

Neurocognition Panel: Initially, the Neurocognition Committee will review all of the tests nominated by experts at the April meeting for consideration in the battery and reduce the list to approximately six tests per neurocognitive domain. The Committee will then select 7 to 15 experts to serve as panelists drawn from different areas of expertise to represent differing views in the field. The panelists will be provided an overview of the relevant scientific literature on each measure to be considered. The scope of the material included in the literature review will be decided by the members of the Neurocognition Committee and will be guided by the survey results from the April conference. The format for presentation of information will also be decided by members of the Committee. Each panelist will be provided information about the candidate tests prior to making their initial ratings. Each test will be evaluated, first in a pre-conference survey, and then at the meeting, according to the criteria agreed upon at the first conference. At the conference, the panelists will be shown how their ratings of the candidate tests compare with those of the rest of the panelists. All entries will be anonymous. The Chair and Co-chair will facilitate discussion of the ratings and elicit input from all panelists. Following discussion, the panelists will re-rate the candidate tests. The ratings will then be tabulated and results summarized shortly after the meeting. The meeting will be open to all interested persons, however only the panelists will be involved in the ratings. The results from the meeting will be summarized in a special article and published in a journal agreed upon by the Neurocognition Committee and NIMH.


Conference #4

NIMH-Industry Collaboration Meeting

Conference Co-Chairs:
Edward Scolnick, M.D., President Emeritus, Merck Research Laboratories
Thomas R. Insel, M.D., Director, National Institute of Mental Health
Herbert Pardes, M.D., Vice Chairman, President & CEO, New York Presbyterian Hospital
Dates and Registration
January 22, 2004
NIMH Neuroscience Center (NSC)
6001 Executive Blvd.
Bethesda, Maryland 20852

Registration: Limited Space on Site

Agenda & Slides

Goals of the Conference
A series of NIH-wide roadmap activities to enhance public-industry-academic collaborations have been recently initiated. In that context, this NIMH meeting has been revised to reflect the specific strategic planning needs in this area. We will address three questions related to NIMH treatment development activities:
  1. Where across the spectrum of drug discovery and development can NIMH play a useful and non-duplicative role in hastening the identification of new treatments for mental illness?
  2. How can the resources of NIMH, including its large clinical trial networks, be used in public private partnerships to address important public health questions and/or hasten treatment development?
  3. What are the major barriers to future intramural and extramural government-industry collaboration and how can they be best overcome?


Conference #5

FDA-NIMH-MATRICS Workshop on Clinical Trial Designs for Neurocognitive Drugs for Schizophrenia

Conference Chair: Robert Buchanan, M.D.

Dates and Registration

April 23 2004
Neuroscience Center, Conference Room C
6001 Executive Boulevard
Rockville, Maryland 20852
 
Registration Open
Agenda
Guidelines from the FDA-NIMH-MATRICS Workshop on Clinical Trial Designs for Neurocognitive Drugs for Schizophrenia
Transcript (WORD)
Transcript (pdf)

Goals of Conference
  1. To develop a consensus among a diverse group of academic and industry scientists as to the most promising clinical trial designs for studying candidate agents that may improve cognition in schizophrenia. This will include both small pilot/proof of concept studies as well as larger controlled trials.
  2. To develop a consensus among the same group of scientists as to the advantages and disadvantages of forming a clinical trials network for the study of agents for improving cognition in schizophrenia.
  3. To develop a consensus among the same group of scientists regarding critical study implementation issues such as characteristics of study populations, including medication status; development of reliability for study instruments; ethical and human use issues; regulatory issues; data management; and other issues.

Conference #6

New Approaches to Assessing and Improving Cognition in Schizophrenia

Conference Chair: Mark Geyer, Ph.D.

Dates and Registration
September 9-10, 2004
Bolger Center
Potomac, MD
Agenda & Slides
Transcript - Day 1
Transcript - Day 2
Goals of Conference
  1. To develop a research agenda that will translate emerging advances in cognitive neurosciences into new strategies for characterizing and quantifying the cognitive impairments in schizophrenia.
  2. To develop a research agenda that will translate emerging advances in cognitive neurosciences into new strategies for identifying promising neural system targets for improving cognition in schizophrenia.
  3. To assess the prospects for developing new imaging-based biomarkers linked to efficacy for improving cognition in schizophrenia.

Matrics Presentations at the International Congress on Schizophrenia Research, April 2005

Michael Green, Ph.D.

Searching for a Co-Primary Measure in Clinical Trials of Cognition Enhancement

Mark Geyer, Ph.D.

Preclinical Discovery of Cognitive Enhancers

Keith Nuechterlein, Ph.D.

Measuring Outcome for Cognitive Enhancement

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Contact matrics.assessment@yahoo.com for questions or comments about the MATRICS program and see our website - www.matricsinc.org - for details regarding the MATRICS Consensus Cognitive Battery (MCCB).

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