drugset / Trial / NCT04659161

A Study to Assess Efficacy and Safety of KarXT in Acutely Psychotic Hospitalized Adult Patients With Schizophrenia (EMERGENT-2)

NCT04659161 ↗

Phase 3 Completed 252 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
2020-12-16
Primary completion
2022-05-24
Completion
2022-05-24

Outcome

Met primary endpoint

paper The trial met the primary endpoint with a mean change from baseline to week 5 in PANSS total score that favoured KarXT PMID 38104575 ↗

registry analysis (superiority test); KarXT vs Placebo; p <0.0001; LS mean difference -9.6 (95% CI -13.9 to -5.2); NCT04659161 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Trospium Small molecule 20 mg Oral
Subject Trospium Small molecule 30 mg Oral
Subject Xanomeline Small molecule 100 mg Oral
Subject Xanomeline Small molecule 125 mg Oral

Indications