drugset / Trial / NCT07422311

To Evaluate the Efficacy, Safety, and Tolerability of Dronabinol Oral Solution for Agitation in Patients With Alzheimer's Disease

NCT07422311

Phase 2/3 Not yet recruiting 140 enrolled Benuvia Therapeutics Inc. Mandara · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

This study tests a medication called dronabinol in people with Alzheimer's disease. First, participants go through up to 4 weeks of screening. Then, over 2 weeks, the dose of the study drug is slowly increased. For the next 10 weeks, participants stay on either dronabinol or a placebo. After finishing this part of the study, participants can join a 6-month extension where everyone receives dronabinol. Those already on the drug stay on their same dose, while those who were on placebo gradually increase their dose over 2 weeks. All participants take dronabinol for the rest of the extension, then complete a final safety check 4 weeks after stopping the medication. Usual medical treatments are continued throughout the study.

Timeline

Start
2026-05-01
Primary completion
2028-05-30
Completion
2028-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Dronabinol Other / unclassified 2.5 mg
Subject Dronabinol Other / unclassified 5 mg
Subject Dronabinol Other / unclassified 9 mg

Indications

No indication recorded.