A Study to Assess the Safety, Tolerability and Pharmacokinetics (PK) of Xanomeline With Trospium Chloride Versus KarXT in Healthy Adult and Elderly Participants of Japanese Ethnicity and to Assess the Effect of Omeprazole on the PK of Xanomeline With Trospium Chloride in Healthy Adult Participants

NCT ID: NCT06605950

Last Updated: 2025-07-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

78 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-01

Study Completion Date

2025-05-31

Brief Summary

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The purpose of this study is to assess the safety, tolerability, and pharmacokinetics (PK) of multiple doses of KarXT + KarX-EC capsules versus KarXT capsules in healthy adult and elderly participants of Japanese ethnicity and to assess the effect of multiple doses of omeprazole on the exposure of xanomeline and trospium administered as KarXT + KarX-EC capsules in healthy adult participants.

Detailed Description

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Conditions

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Healthy Volunteers

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors
Part 1 of this study is double-blind while Part 2 is open-label.

Study Groups

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Group A

Group Type EXPERIMENTAL

KarXT

Intervention Type DRUG

Specified dose on specified days

Placebo

Intervention Type DRUG

Specified dose on specified days

Group B

Group Type EXPERIMENTAL

KarXT

Intervention Type DRUG

Specified dose on specified days

Placebo

Intervention Type DRUG

Specified dose on specified days

Group C

Group Type EXPERIMENTAL

KarXT

Intervention Type DRUG

Specified dose on specified days

KarX-EC

Intervention Type DRUG

Specified dose on specified days

Placebo

Intervention Type DRUG

Specified dose on specified days

Group D

Group Type EXPERIMENTAL

KarXT

Intervention Type DRUG

Specified dose on specified days

KarX-EC

Intervention Type DRUG

Specified dose on specified days

Omeprazole

Intervention Type DRUG

Specified dose on specified days

Interventions

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KarXT

Specified dose on specified days

Intervention Type DRUG

KarX-EC

Specified dose on specified days

Intervention Type DRUG

Placebo

Specified dose on specified days

Intervention Type DRUG

Omeprazole

Specified dose on specified days

Intervention Type DRUG

Other Intervention Names

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BMS-986510 Xanomeline/Trospium Chloride BMS-986519 Xanomeline Enteric-coated

Eligibility Criteria

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Inclusion Criteria

* Healthy adult participants must be 19 to 55 years of age, inclusive.

i) Both participant's biological parents are of ethnic Japanese ancestry. Participants must be first generation Japanese.

ii) Must have a body mass index (BMI) of 18.0 to 32.0 kg/m2 (inclusive), at the time of signing the ICF.

iii) Must have an estimated glomerular filtration rate (eGFR) of ≥ 90 mL/min/1.73m2 by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation at the screening visit. One repeat measurement is allowed.

* Healthy elderly participants must be 56 to 90 years of age, inclusive.

i) Both participant's biological parents are of ethnic Japanese ancestry. Participants must be first generation Japanese.

ii) Must have a BMI ≥ 18.0 and ≤ 35.0 kg/m2 (inclusive), at the time of signing the ICF.

iii) Must have an eGFR of \> 60 mL/min/1.73m2 by the CKD-EPI equation at the screening visit. One repeat measurement is allowed.

* Healthy adult participants must be 19 to 55 years of age, inclusive.

i) Participants with any ethnicity can be included.

ii) Must have a BMI of 18.0 to 32.0 kg/m2 (inclusive), at the time of signing the ICF.

iii) Must have an eGFR of ≥ 90 mL/min/1.73m2 by the CKD-EPI equation at the screening visit. One repeat measurement is allowed.

Exclusion Criteria

i) Participant is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study.

ii) History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI or designee.

iii) Participant has a history of syncope and/or symptomatic orthostatic hypotension in the year prior to Day 1.

iv) History of cancer that has not been in full remission for \>5 years (except basal cell skin cancer or squamous cell skin cancer with history of curative treatment and no recurrence for \> 1 year prior to the screening visit).
Minimum Eligible Age

19 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Karuna Therapeutics

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Bristol-Myers Squibb

Locations

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Cenexel ACT (Anaheim Clinical Trials)

Anaheim, California, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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CN012-0030

Identifier Type: -

Identifier Source: org_study_id

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