U.S., March 21 -- ClinicalTrials.gov registry received information related to the study (NCT06885567) titled 'A Phase 2 Study to Evaluate the Safety and Efficacy of BEY2153 in Patients with Early Alzheimer's Disease' on March 10.
Brief Summary: The purpose of this study is to investigate the safety and efficacy of BEY2153 in patients with early Alzheimer's Disease. Subjects who meet the inclusion and exclusion criteria will be randomized 1:1:1 to one of three treatment arms for 26 weeks administration. The extension study for additional 26 weeks will be conducted open-label with one treatment arm. Subjects will take BEY2153 orally once a day during the study.
Study Start Date: July, 2025
Study Type: INTERVENTIONAL
Condition:
Alzheimer ...