drugset / Trial / NCT07633470

A Study of Zunveyl on Safety, Tolerability, Neuropsychiatric Symptoms, and Caregiver Distress in Alzheimer's Disease (RESOLVE)

NCT07633470 ↗

Phase 4 Recruiting 150 enrolled Alpha Cognition, Inc
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the safety and tolerability of Zunveyl® over 12 weeks of routine clinical use in adults with mild to moderate Alzheimer's disease.

Timeline

Start
2026-05-20
Primary completion
2027-04
Completion
2027-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Zunveyl® Small molecule 10 mg Oral

Indications