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Clinical Trial Summary

The purpose of this study is to find out the time it takes to absorb, distribute, breakdown and remove the drug from the body in healthy participants and subjects with schizophrenia and whether it causes any side effects.


Clinical Trial Description

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetic profile of ascending multiple oral doses of AMG 581 in healthy subjects or subjects with schizophrenia or schizoaffective disorder on antipsychotic medication. The study will also assess the effects of AMG 581 on midazolam PK in healthy subjects or subjects with schizophrenia or schizoaffective disorder on antipsychotic medication. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02504476
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 1
Start date August 2015
Completion date February 2016

See also
  Status Clinical Trial Phase
Completed NCT02567370 - Single-ascending Dose Study With a Food-Effect Cohort to Evaluate AMG 581 Phase 1
Recruiting NCT01016145 - Identifying Predictors of Response to Antipsychotics Using a Treatment Algorithm Phase 4