22nd Annual Scientific Meeting

18 – 20 February, 2026   //   Washington DC

Distinguished Poster Award Recipient:

Siegel – Precision Imaging Drug Trials: Quantifying the Impact of Study Design on fMRI Biomarker Sensitivity and Statistical Power (Abstract)

 

All Poster PDFs and Abstracts are available here

 

 18 February 2026

   
 Welcome from the President Luca Pani
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Keynote Address: CDER Office of Neuroscience Valentina Mantua
Michelle Campbell
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New Investigator Award Presentations
(Day 1)
Judith Jaeger
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Jamie Courtland
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Claire Erickson
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Morgan Hardy
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Keiko Kunitoki
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Yoojin Lee
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video – All Presenters
 
Methodological opportunities and challenges with long-term post-marketing data Chairs:
Ole Andreassen
Jenicka Engler
Shaheen Lakhan
 
  Introduction 

Jenicka Engler
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  Long-term medical outcomes of antipsychotic treatment

Mark Weiser
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  Use of large real-world databases: Opportunities and challenges Ole Andreassen
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  Safety trial methodology considerations for novel mechanisms of action in psychiatry trials Tejendra Patel
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  Integrated evidence generation planning: Leveraging AI and real-world evidence to advance science Mandeep Kaur
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  Regulatory perspective Wei Hua
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  Panel Discussion All speakers
Facilitator:
Shaheen Lakhan

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Wednesday Working Group Sessions 

   
  Advancing the methods to evaluate abuse and dependence-potential in clinical studies for CNS-active drugs and novel psychedelics Chairs:
Jadwiga Martynowicz
Beatrice Setnik

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  Behavioral and psychiatric symptoms in dementia (BPSD): Apathy/Agitation Chairs:
Krista Lanctôt
David Miller
summary
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  Defining and standardizing vocal biomarker outcomes Chairs:
Alex Cohen
Jan Sedway

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  Workshop: Identifying and addressing hurdles to the introduction of new treatments and methodology into clinical practice Chairs:
Larry Alphs
Ara Khachaturian
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  Orphan diseases Chairs: 
Joan Busner
Gahan Pandina
summary
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  Sleep methodology in CNS trials Chairs:
Georg Dorffner
Margaret Moline
summary
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19 February 2026

 
New Investigator Award Presentations
(Day 2)
Judith Jaeger
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Julia Longenecker
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Zev Nakamura
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Aikaterina Stravoravdi
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Amy Wegener
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video – All Presenters
 
Lewis Alan Opler Prize Presentations Gary Sachs
Mark Opler
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Cecilia Bergeria
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Sunny Tang
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video – All Presenters
 
Emerging value and pitfalls of large language models in drug development Chairs:
Anzar Abbas
Amir Kalali

 
  LLMs: Good or bad? Amir Kalali
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  Introduction to session Anzar Abbas
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  Use of LLMs for oversight in a phase 3 clinical development program

Todd Solomon
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  Automated monitoring of dosing and other sessions in psychedelic trials using LLMs Atul Mahableshwarkar
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  Novel methods to quantify changes in schizophrenia symptoms using PANSS interview transcripts Jeffrey Cochran
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  The application of artificial intelligence/machine learning in drug development and regulation Ruihao Huang
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  Panel Discussion All speakers
Panelist:
Valentina Mantua
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Use of regulatory flexibility to accelerate drug development Chairs: 
Kemi Olugemo
Siân Ratcliffe Smethurst
 
  Introduction Kemi Olugemo
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  Path to prevention (P2P) therapeutics platform trial in early neuronal synuclein disease (NSD) Christopher Coffey
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  Use of external controls for the primary analysis of a randomized phase 3 study to evaluate a higher dose regimen of nusinersen for the treatment of spinal muscular atrophy (SMA) Richard Foster*
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  Prognostic adjustment and other digital twin methods for improving trial efficiency Roland Brown
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  Surrogate endpoint in Alzheimer’s disease Tianle Chen
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  Precision medicine at scale: Operationalizing individualized trials Sarah Glass
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  Panel Discussion 

All speakers
Facilitators:
Kemi Olugemo
Luca Pani

Panelist:
Emily Freilich
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The power of inclusion in clinical trials: It’s time to study all people, even if they have thought about suicide Chairs:
Jill Harkavy-Friedman
Manish Jha
 
  Introduction: Goals of session and key issues to be addressed Jill Harkavy-Friedman
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  The goal of clinical trials that include suicidal people is not just prediction of risk Manish Jha
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  Current approach to including individuals with suicidal ideation and behavior (SIB) in clinical trials Steven Szabo
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  Including people with suicidal ideations and behaviors in CNS clinical trials: Regulatory perspectives Zimri Yaseen
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  Panel Discussion with Jha, Szabo, and Yaseen Panel
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  Psychometric and statistical considerations for including patients with SI/B in clinical trials Kari Nations
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  Implementation of suicide research into clinical settings Elizabeth Ballard
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  Ecological momentary assessment of suicidal ideation and behavior in trials Evan Kleiman
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  Clinically based suicide prevention: Veterans Affairs Health System suicide analytics and the REACH VET clinical program John McCarthy
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  Panel Discussion All speakers
Facilitators:
Jill Harkavy-Friedman
Manish Jha
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 Poster Session/Reception Poster PDFs and Abstracts  

20 February 2026

 

Friday Working Group Sessions 

   
  Development of novel endpoints for clinical trials in substance use disorders  Chairs: 
Martin Mumenthaler
Tanya Ramey
summary
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  Emerging value and challenges of large language models (LLMs) in drug development  Chairs: 
Anzar Abbas
Amir Kalali
 
  Estimands and missing data  Chairs:
Elena Polverejan
Lorenzo Guizzaro

summary
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  Accelerating development of psychopathology measures- ISCTM/ECNP joint working group:
Subgroup meetings
Chairs:
Jenicka Engler
Nina Schooler
Celso Arango
 
  Bipolar disorder subgroup (Manpreet Singh, Eduard Vieta) Bipolar subgroup summary  
  MDD subgroup (Jenicka Engler, Stephanie Sommer) MDD subgroup summary  
  Schizophrenia subgroup (Anzalee Khan, Armida Mucci, Simon Desjardins)    
Development, validation, and qualification of novel clinical endpoints Chairs:
Adam Butler
Sonya Eremenco         
 
  Introduction Adam Butler
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  Development and qualification of the Virtual Reality Functional Capacity Assessment Tool-Short List for early Alzheimer’s disease Sonya Eremenco
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  Qualification plan for the PSYCHS as a ClinRO for attenuated positive symptoms in patients at clinical high risk for psychosis Scott Woods
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  Qualification of depression and anxiety AI-COA through ISTAND Marc Aafjes
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  Patient perspective on clinical trials and rating scales Emma C.
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  Regulatory perspectives: Development and qualification of novel drug development tools Michelle Campbell
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  Panel Discussion All speakers
Facilitator:
Adam Butler
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  Meeting Adjourned

Atul Mahableshwarkar
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  *Video not released