HomeTrialNCT07204418
🔬NCT07204418Phase 1RECRUITING

A Study to Evaluate the Effects of CYP2D6 Phenotypes on the Pharmacokinetics of Xanomeline Following KarXT Administration in Healthy Adult Participants

Study Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) of xanomeline following administration of KarXT in CYP2D6 normal/extensive, intermediate, poor, and ultrarapid metabolizers.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment56 participants
Primary Completion
Lead SponsorKaruna Therapeutics, Inc., a Bristol Myers Squibb company
Data Retrieved2026-04-11 04:08:14.746188+00:00
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