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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
Authors not listed
Alpha Cognition, Inc · 2026
Abstract
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.
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- 2026-10-26 MST
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APA
Anonymous. (2026). 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. <em>Alpha Cognition, Inc</em>. https://clinicaltrials.gov/study/NCT07633470
Vancouver
Anonymous. 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. Alpha Cognition, Inc. 2026.
BibTeX
@misc{anon2026RESOLV,
title = {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},
author = {Anonymous},
journal = {Alpha Cognition, Inc},
year = {2026},
}
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