Small molecule · Agonist of M1 muscarinic acetylcholine receptor (CHRM1) and M4 muscarinic acetylcholine receptor (CHRM4) · developed by E.R. Squibb & Sons, L.L.C.
Xanomeline is a muscarinic acetylcholine receptor agonist that acts on M1 and M4 receptors in the central nervous system. It is combined with trospium chloride, a peripheral muscarinic antagonist, to reduce peripheral side effects.
Summary written with AI from the sources listed at the end of this page.
From the indications section of the FDA label (version of Jan 16, 2026). Read the full label for the exact wording, limitations and safety information.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT07686263 | Phase 3 | Schizophrenia | Recruiting | BMY |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Schizophrenia
Updated Oct 3, 2026. Something wrong or missing? Report it on the BMY page.
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