RecruitingPhase 1NCT07063342

A Study to Evaluate Novel KarX and KarT Prototypes Versus the KarXT and KarX-EC Reference Following Single Doses, and to Explore the Effect of Food After Multiple Doses of Selected Prototypes in Healthy Adult Participants

Phase 1, 3-Part, Open-label Study to Evaluate the Pharmacokinetics of Novel KarX (BMS-986519) and KarT (BMS-986520) Prototypes Versus the KarXT (BMS-986510) and KarX-EC (BMS-986519) Reference Following Single Doses, and to Explore the Effect of Food After Multiple Doses of Selected Prototypes in Healthy Adult Participants


Sponsor

Bristol-Myers Squibb

Enrollment

72 participants

Start Date

Jun 27, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate novel KarX and KarT prototypes versus the KarXT and KarX-EC reference following single doses, and to explore the effect of food after multiple doses of selected prototypes in healthy adult participants.


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Inclusion Criteria1

  • BMI between 18.0 kg/m2 to 32.0 kg/m2, inclusive, at screening.

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Interventions

DRUGXanomeline/Trospium Chloride Capsule

Specified dose on specified days

DRUGXanomeline Enteric Capsule

Specified dose on specified days

DRUGTrospium Chloride

Specified dose on specified days


Locations(1)

Quotient Sciences

Nottingham, Nottinghamshire, United Kingdom

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NCT07063342


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