RECRUITING Phase 4 ClinicalTrials.gov

Study to Assess Safety and Tolerability of KarXT With Administration of Antiemetics in Healthy Volunteers

Sponsor: Karuna Therapeutics, Inc., a Bristol Myers Squibb company • ClinicalTrials.gov ID: NCT07681076

Registry updated: 2026-10-15

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Description

This study looks at how to reduce nausea and vomiting in people taking KarXT which is used to treat mental health conditions like schizophrenia. KarXT can cause stomach-related side effects, especially in the first couple of weeks. In this study, healthy volunteers will take KarXT along with anti-nausea medication, either regularly (to prevent symptoms) or as needed. The goal is to see how well these strategies help reduce nausea and vomiting and how safe the combination is. The results will help doctors better manage side effects and make treatment more comfortable for patients starting KarXT.

Interventions

KarXT (Drug)
Specified dose on specified days
Trimethobenzamide (Drug)
Specified dose on specified days
Ondansetron (Drug)
Specified dose on specified days
Meclizine (Drug)
Specified dose on specified days

Eligibility criteria

Inclusion Criteria: * Participants must be healthy male and female participants as determined by no clinically significant deviation from normal in medical history, physical examination, 12-lead ECG, VS, and clinical laboratory determinations. * Participants must be willing and able to be confined to an inpatient setting for a 3-week duration, follow instructions, and comply with the protocol requirements. * Participants must have BMI ≥ 18 and ≤ 40 kg/m2. * Individuals of childbearing potential (IOCBP) must be willing and able to adhere to the contraception guidelines. Exclusion Criteria: * Participants must not have history or presence of clinically significant cardiovascular (eg, untreated or unstable hypertension, clinically significant tachycardia), pulmonary, renal, hematologic, gastrointestinal (\[GI\] eg, obstructive disorders \[including conditions that may decrease GI motility, such as ulcerative colitis, intestinal atony, and myasthenia gravis\], active biliary disease \[including symptomatic gallstones\]), endocrine, immunologic, dermatologic, neurologic, or oncologic disease or any other condition that, in the opinion of the investigator, would jeopardize the safety of the participant or the validity of the study results. * Participants must not have history of moderate to severe alcohol use disorder or a substance (other than nicotine or caffeine) use disorder within the past 12 months or a positive urine drug screen (UDS) for a substance other than cannabis at screening or baseline. * Participants must not have history or high risk of urinary retention, gastric retention, or narrow-angle glaucoma. * Participants must not have active biliary disease (eg, symptomatic gallstones). Participants with other biliary histories are eligible and should be discussed with the medical monitor. * Other protocol-defined Inclusion/Exclusion criteria apply.

Conditions

Healthy Volunteers

Locations

Collaborative Neuroscience Network - Los Alamitos- CenExel - PPDS — Los Alamitos, California, United States
CenExel RCA - Hollywood — Hollywood, Florida, United States
Atlanta Center for Medical Research - CenExel ACMR - PPDS — Atlanta, Georgia, United States
iResearch Atlanta - CenExel - PPDS — Decatur, Georgia, United States

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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