drugset / Trial / NCT04738123

A Study to Assess Efficacy and Safety of KarXT in Acutely Psychotic Hospitalized Adult Patients With Schizophrenia (EMERGENT-3)

NCT04738123

Phase 3 Completed 256 enrolled Karuna Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 3, randomized, double-blind, parallel-group, placebo-controlled, multicenter inpatient study to examine the efficacy and safety of KarXT in adult subjects who are acutely psychotic with a Diagnostic and Statistical Manual Fifth Edition (DSM-5) diagnosis of schizophrenia. The primary objective of the study is to assess the efficacy of KarXT (a fixed combination of xanomeline 125 mg and trospium chloride 30 mg twice daily \[BID\]) versus placebo in reducing Positive and Negative Syndrome Scale (PANSS) total scores in adult inpatients with a DSM-5 diagnosis of schizophrenia. The secondary objectives of the study are to evaluate improvement in disease severity and symptoms, safety and tolerability, and pharmacokinetics in adult inpatients with a DSM-5 diagnosis of schizophrenia.

Timeline

Start
2021-04-06
Primary completion
2022-11-29
Completion
2022-12-07

Drugs

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

Indications