Clinical trials of potential cognitive-enhancing drugs in schizophrenia: what have we learned so far?
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Richard S E Keefe1, Robert W Buchanan, Stephen R Marder
1Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA. richard.keefe@duke.edu
Abstract:
In light of the number of studies conducted to examine the treatment of cognitive impairment associated with schizophrenia (CIAS), we critically reviewed recent CIAS trials. Trials were identified through searches of the website "www.clinicaltrials.gov" using the terms "schizophrenia AND cognition," "schizophrenia AND neurocognition," "schizophrenia AND neurocognitive tests," "schizophrenia AND MATRICS," "schizophrenia AND MCCB," "schizophrenia AND BACS," "schizophrenia AND COGSTATE," and "schizophrenia AND CANTAB" and "first-episode schizophrenia AND cognition." The cutoff date was 20 April 2011. Included trials were conducted in people with schizophrenia, the effects on cognition were either a primary or secondary outcome, and the effect of a pharmacologically active substance was examined. Drug challenge, pharmacokinetic, pharmacodynamic, or prodrome of psychosis studies were excluded. We identified 118 trials, with 62% using an add-on parallel group design. The large majority of completed trials were underpowered to detect moderate effect sizes, had ≤8 weeks duration, and were performed in samples of participants with chronic stable schizophrenia. The ongoing add-on trials are longer, have larger sample sizes (with a number of them being adequately powered to detect moderate effect sizes), and are more likely to use a widely accepted standardized cognitive battery (eg, the MATRICS Consensus Cognitive Battery) and MATRICS guidelines. Ongoing studies performed in subjects with recent onset schizophrenia may help elucidate which subjects are most likely to show an effect in cognition. New insights into the demands of CIAS trial design and methodology may help increase the probability of identifying treatments with beneficial effect on cognitive impairment in schizophrenia.
Insights
This review found most schizophrenia cognitive impairment trials were underpowered and short. Ongoing trials are improving methodology, sample size, and duration for better treatment discovery.
Area of Science:
- Psychiatry
- Clinical Trials
- Neuroscience
Background:
- Cognitive impairment is a core symptom of schizophrenia.
- Numerous clinical trials have investigated treatments for cognitive impairment associated with schizophrenia (CIAS).
- Critical review of trial design and methodology is needed to improve treatment discovery.
Purpose of the Study:
- To critically review recent clinical trials for CIAS.
- To identify trends in trial design, methodology, and power.
- To inform future CIAS trial design for increased success.
Main Methods:
- Searched clinicaltrials.gov for CIAS trials up to April 20, 2011.
- Included trials examining pharmacologically active substances with cognition as an outcome.
- Excluded drug challenge, pharmacokinetic, pharmacodynamic, or prodrome studies.
Main Results:
- Identified 118 trials; 62% used add-on parallel group design.
- Most completed trials were underpowered, short (≤8 weeks), and used chronic stable schizophrenia samples.
- Ongoing trials show improvements in duration, sample size, power, and use of standardized batteries (e.g., MATRICS Consensus Cognitive Battery).
Conclusions:
- Past CIAS trials often lacked the power and duration to detect meaningful treatment effects.
- Current and future trials are adopting more robust designs, including larger sample sizes and standardized cognitive assessments.
- Focusing on early-onset schizophrenia and refining trial methodologies may enhance the identification of effective treatments for cognitive impairment in schizophrenia.
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