An Open-label Long-term Safety Study of Buntanetap in Participants With AD
- Sponsor
- Annovis Bio Inc.
- Study ID
- NCT07757204
- Phase
- PHASE2/PHASE3
- Status
- Not Yet Recruiting
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Conditions
- Alzheimer's Dementia (AD)
Eligibility Criteria
- Sex
- ALL
- Age
- 55 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- buntanetap/posiphen — DRUGbuntanetap 30 mg daily
Study Details
This study will examine the long-term safety of buntanetap in participants with AD who have participated in a prior study of buntanetap in AD.
Key Dates
- First listed
- Aug 11, 2026
- Start date
- Sep 21, 2026
- Status verified
- Jul 2026
- Primary completion
- Feb 21, 2030
- Completion
- May 31, 2030
Study Design
- Enrollment
- 400 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Single ArmAll participants receive buntanetap 30 mg qd
Primary Outcome Measure
Safety of buntanetap [ Time Frame: 24 months of treatment ]
Central Contacts
- Sarah MacCallum, BSN RN484-875-3192
- Alexander Morin, PhD484-875-3192
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