Phase 2Recruiting

Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986368, for the Treatment of Agitation in Participants With Alzheimer's Disease

A Phase 2, Randomized, Double-blind, Three-Arm, Placebo-controlled, Multicenter Study Assessing the Efficacy, Safety and Tolerability of Orally Administered BMS-986368, a FAAH/MAGL Inhibitor, for the Treatment of Agitation in Participants With Alzheimer's Disease (BALANCE-AAD-1)

Sponsor
Celgene (Industry)
Enrolment
120 planned
Conditions
Agitation; Alzheimer Disease
Interventions
BMS-986368; Placebo
Ages
adults, older adults
Registry
NCT06808984

From the registry

This is a study to evaluate the efficacy, safety, and tolerability of BMS-986368, a FAAH/MAGL inhibitor, for the treatment of agitation in participants with Alzheimer's Disease.

Primary outcomes

  • Change in Cohen-Mansfield Agitation Inventory (CMAI) total score from baseline
Full record on ClinicalTrials.gov