zunveyl
zunveyl: developed by 1 company · 1 clinical trial tracked · 1 FDA decision.
zunveyl evidence translation
What we can confirm
1 FDA record · 1 tracked trial
What it means
What to watch
Prepared research question
How could zunveyl → ACOG affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence1 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (1)
| Company | Phase |
|---|---|
| Alpha Cognition Inc. (ACOG) | Phase 4 |
Clinical Trials (1)
RESOLVE: A Phase 4, Open-label Study to Assess the Effect of Zunveyl on Safety and Tolerability, Neuropsychiatric Symptoms, and Caregiver Distress in Adults With Mild to Moderate Alzheimer's Disease
Primary endpoint: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
FDA Decisions1 records
Frequently asked questions
Who is developing zunveyl?
zunveyl is being developed by Alpha Cognition Inc..
How many clinical trials involve zunveyl?
BioSniper tracks 1 clinical trial involving zunveyl.
What is zunveyl's latest FDA decision?
The most recent tracked FDA decision for zunveyl is Approval for 1 INDICATIONS AND USAGE ZUNVEYL is indicated for the treatment of mild to moderate dementia of the Alzheimer's type in adults. ZUNVEYL is a cholinesterase inhibitor indicated for the treatment of mild to moderate dementia of the Alzheimer's type in adults ( 1 ), dated July 26, 2024.