drugset / Trial / NCT03697252

A Study to Assess Safety and Efficacy of KarXT in Adult Patients With Schizophrenia

NCT03697252

Phase 2 Completed 182 enrolled Karuna Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2, randomized, double-blinded, placebo-controlled, inpatient study to examine the efficacy, safety, and tolerability profile of KarXT in adult subjects diagnosed with DSM-5 schizophrenia who are in an acute exacerbation phase. The primary objective of the study is to assess the efficacy of KarXT (a fixed combination of xanomeline and trospium chloride) (xanomeline 125 mg/trospium 30 mg twice daily \[BID\]) versus placebo in reducing Positive and Negative Syndrome Scale (PANSS) total scores in adult inpatients with a Diagnostic and Statistical Manual-Fifth Edition (DSM-5) diagnosis of schizophrenia. The secondary objectives of the study are to assess overall safety and tolerability of KarXT in adult inpatients with a DSM-5 diagnosis of schizophrenia.

Timeline

Start
2018-09-18
Primary completion
2019-09-04
Completion
2019-09-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Trospium Small molecule 30 mg Oral
Subject Xanomeline Small molecule 125 mg Oral

Indications