drugset / Trial / NCT03356639

A Study to Assess the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of ASP6981 in Subjects With Schizophrenia

NCT03356639 ↗

Phase 1 Completed 32 enrolled Astellas Pharma Global Development, Inc.
RandomizedCrossoverDouble-blindTreatment

Summary

The primary purpose is to evaluate the safety and tolerability of ASP6981 in participants with schizophrenia. Also primary purpose is to evaluate the pharmacodynamics of ASP6981 in participants with schizophrenia as measured by cognitive function and neurophysiological biomarkers. The secondary purpose of this study is to evaluate the pharmacokinetics of ASP6981 in participants with schizophrenia.

Timeline

Start
2018-01-22
Primary completion
2018-05-30
Completion
2018-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP6981 Unknown 50 mg Oral
Subject ASP6981 Unknown 135 mg Oral

Indications