A Study to Evaluate KYN-5356 in Adults With Cognitive Impairment Associated With Schizophrenia

Recruiting Phase 2 Interventional Study
Cognitive Impairment Associated With Schizophrenia (CIAS)
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 55
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Kynexis B.V. · Industry
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About This Trial
This is a Phase 2, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety, Pharmacokinetic (PK) and Pharmacodynamic (PD) effects of 3 different dose regiments of KYN-5356 and placebo for 28 days. Participants will be randomized to one of 4 treatment groups: placebo, KYN-5356 low dose, KYN-5356 medium dose, KYN-5356 high dose. Participants will be admitted to the clin…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Has an established primary psychiatric diagnosis of schizophrenia * Clinically stable and in the residual (nonacute) phase of their illness for at least 8 weeks before screening in the judgement of the investigator * Diagnosis of schizophrenia for at least 1 year before screen…
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