A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Orally Administered ML-007C-MA in Inpatient Adult Participants With Schizophrenia Experiencing an Acute Exacerbation of Psychosis
Latest Information Update: 22 Jul 2025
At a glance
- Drugs ML 007/muscarinic antagonist (Primary)
- Indications Schizophrenia
- Focus Therapeutic Use
- Acronyms ZEPHYR
- Sponsors MapLight Therapeutics
Most Recent Events
- 09 Jul 2025 Status changed from not yet recruiting to recruiting.
- 07 Jul 2025 According to MapLight Therapeutics media release, company announced the initiation of a Phase 2 study to evaluate the efficacy, safety and tolerability of ML-007C-MA. The Phase 2 ZEPHYR study has been designed based on the results of an extensive Phase 1 development program that included 270 healthy volunteers.
- 05 Jul 2025 New trial record