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xanomeline

Generic: xanomeline·Brand: Cobenfy

xanomeline: 9 clinical trials tracked.

xanomeline evidence translation

What we can confirm

9 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about xanomeline, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 1 study sponsors
Clinical Trial Registry Records (9)

A Prospective, Observational, Single-Arm, Multicenter Real-World Study Evaluating the Treatment Pattern, Safety and Effectiveness of Xanomeline and Trospium Chloride Capsules (KarXT) in the Treatment of Chinese Adult Participants With Schizophrenia

NCT07802132Registry updated 2026-09-03
Not yet recruiting

Primary endpoint: KarXTtreatment pattern according to clinicians'decision

Observational250 targetStarted 2026-09Completion 2028-12Zai Lab (Shanghai) Co., Ltd.

A Multimodal PET/MRI Study of Cobenfy on Dopamine Transmission in Schizophrenia

NCT07423546Registry updated 2026-07-14·Phase 1/Phase 2
Recruiting

Primary endpoint: [18F]DOPA Kicer ([18F]DOPA relative uptake rate)

InterventionalRandomizedquadruple12 targetStarted 2026-07Completion 2027-121 site · United StatesNew York State Psychiatric Institute

Effectiveness and Adverse-effect Switch Evaluation

NCT07379827Registry updated 2026-08-19·BMY
Recruiting

Primary endpoint: Treatment titration and switch regimens as described by the prescribing clinician

Observational1,500 targetStarted 2026-02Completion 2028-0650 sites · United StatesBristol-Myers Squibb

Real-world Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)

NCT07101094Registry updated 2026-09-30·BMY
Recruiting

Primary endpoint: Participant medication preference as assessed by the Preference of Medication (POM) questionnaire

Observational300 targetStarted 2025-09Completion 2029-0520 sites · United StatesBristol-Myers Squibb

Phase 1, 4-Part, Open-label (Parts 1 to 3) and Double-blind (Part 4) 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, and to Evaluate Alternative Formulations of KarX (BMS-986519) and KarXT (BMS-986510) Following Single and Multiple Ascending Doses in Healthy Adult Participants

NCT07063342Registry updated 2026-08-17·Phase 1·BMY
Recruiting

Primary endpoint: Maximum observed concentration (Cmax)

InterventionalRandomizedopen236 targetStarted 2025-06Completion 2027-031 site · United KingdomBristol-Myers Squibb

A Phase 3, Multicenter, Two-part Study With a 5-week Double-blind Part (Randomized, Parallel-group, Placebo-controlled) Followed by a 12-week Open-label Extension Part, to Evaluate the Efficacy and Safety of KarXT in Acutely Psychotic Hospitalized Chinese Adult Subjects With DSM-5 Schizophrenia

NCT05919823Registry updated 2025-12-17·Phase 3
Completed

Primary endpoint: Change From Baseline in Positive and Negative Syndrome Scale (PANSS) Total Scores at Week 5 of the Double-Blind Period

InterventionalRandomizedtriple202 enrolledStarted 2023-05Completion 2024-1228 sites · ChinaKaruna Therapeutics, Inc., a Bristol Myers Squibb company

An Open-label Extension Study to Assess the Long-term Safety and Tolerability of Adjunctive KarXT in Subjects With Inadequately Controlled Symptoms of Schizophrenia

NCT05304767Registry updated 2026-07-31·Phase 3
Completed

Primary endpoint: Incidence of treatment-emergent adverse events (TEAEs)

Interventionalopen290 enrolledStarted 2022-03Completion 2026-0350 sites · United StatesKaruna Therapeutics, Inc., a Bristol Myers Squibb company

A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of Adjunctive KarXT in Subjects With Inadequately Controlled Symptoms of Schizophrenia

NCT05145413Registry updated 2026-05-05·Phase 3
Completed

Primary endpoint: Change From Baseline in Positive and Negative Syndrome Scale (PANSS) Total Score at Week 6

InterventionalRandomizedquadruple396 enrolledStarted 2021-11Completion 2025-0350 sites · United StatesKaruna Therapeutics, Inc., a Bristol Myers Squibb company

An Open-label Study to Assess the Long-term Safety, Tolerability, and Efficacy of KarXT in De Novo Subjects With DSM-5 Schizophrenia

NCT04820309Registry updated 2025-09-17·Phase 3
Completed

Primary endpoint: Number of Participants With Treatment Emergent Adverse Events (TEAEs)

Interventionalopen566 enrolledStarted 2021-06Completion 2024-0550 sites · United StatesKaruna Therapeutics, Inc., a Bristol Myers Squibb company