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
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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COMPLETED
PHASE1
78 participants
INTERVENTIONAL
2024-10-01
2025-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Group A
KarXT
Specified dose on specified days
Placebo
Specified dose on specified days
Group B
KarXT
Specified dose on specified days
Placebo
Specified dose on specified days
Group C
KarXT
Specified dose on specified days
KarX-EC
Specified dose on specified days
Placebo
Specified dose on specified days
Group D
KarXT
Specified dose on specified days
KarX-EC
Specified dose on specified days
Omeprazole
Specified dose on specified days
Interventions
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KarXT
Specified dose on specified days
KarX-EC
Specified dose on specified days
Placebo
Specified dose on specified days
Omeprazole
Specified dose on specified days
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
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
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).
19 Years
90 Years
ALL
Yes
Sponsors
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Karuna Therapeutics
INDUSTRY
Responsible Party
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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
Countries
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Related Links
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BMS Clinical Trial Information
BMS Clinical Trial Patient Recruiting
Other Identifiers
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CN012-0030
Identifier Type: -
Identifier Source: org_study_id
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