A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Study Evaluating the Safety and Efficacy of Simufilam 100 Mg Tablets in Subjects with Mild-to-Moderate Alzheimer's Disease
Latest Information Update: 11 Oct 2024
At a glance
- Drugs Simufilam (Primary)
- Indications Alzheimer's disease; Dementia
- Focus Registrational; Therapeutic Use
- Acronyms RETHINK-1; RETHINK-ALZ
- Sponsors Cassava Sciences
- 08 Oct 2024 Planned End Date changed from 1 Oct 2024 to 15 Oct 2024.
- 08 Oct 2024 Planned primary completion date changed from 1 Oct 2024 to 15 Oct 2024.
- 25 Sep 2024 According to a Cassava Sciences media release, the company announced the completion of a third interim patient safety review by an Independent Data and Safety Monitoring Board (DSMB). DSMB recommended that trial continue as planned, without modification. Topline data from this trial expected before year end 2024. Final safety data are expected at the conclusion of the Phase 3 program.