drugset / Trial / NCT05304767

An Extension Study to Assess Long-Term Safety and Tolerability of Adjunctive KarXT in Subjects With Inadequately Controlled Symptoms of Schizophrenia

NCT05304767

Phase 3 Recruiting 280 enrolled Karuna Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase 3, multicenter, 52-week, outpatient, open-label extension (OLE) study to evaluate the long-term safety and tolerability of adjunctive KarXT in subjects with schizophrenia with an inadequate response to their current antipsychotic treatment who previously completed the treatment period (Visit 8/Day 42 ± 3) of ARISE Study (KAR-012). The primary objective of the study is to assess the long-term safety and tolerability of adjunctive KarXT (a fixed dose combination of xanomeline and trospium chloride twice daily \[BID\]) in subjects with schizophrenia.

Timeline

Start
2022-03-07
Primary completion
2026-03-19
Completion
2026-03-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Trospium Small molecule 20 mg
Subject Trospium Small molecule 30 mg
Subject Xanomeline Small molecule 50 mg
Subject Xanomeline Small molecule 75 mg
Subject Xanomeline Small molecule 100 mg
Subject Xanomeline Small molecule 125 mg

Indications