CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 564 enrolled
Drug / intervention
SUVN-502 +3 moredrug
Likely dose
Donepezil 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02580305
NCT02580305Phase 2Completed

A Phase 2a Multicenter, Randomized, Double-Blind, Parallel Group, 26-Week, Placebo-Controlled Study of SUVN-502 in Subjects With Moderate Alzheimer's Disease Currently Treated With Donepezil Hydrochloride and Memantine Hydrochloride

Suven Life Sciences Limited·interventional·Posted Oct 20, 2015·Updated Jun 9, 2023

In Brief

A Phase 2 clinical trial evaluating SUVN-502, Placebo, and 2 other interventions for Alzheimer's Disease. Completed, enrolled 564 participants across 71 sites.

Detailed Summary

This is a phase 2a, proof-of-concept, 26-week, double-blind, multicenter, randomized, parallel group, placebo-controlled study to compare the efficacy and safety of treatment with SUVN-502 to placebo treatment in subjects with moderate Alzheimer's disease receiving stable doses of donepezil HCl and memantine HCl.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedOct 20, 2015
Enrollment StartSep 1, 2015
Primary CompletionNov 5, 2019
Study CompletionNov 7, 2019
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 10.7 years ago

Interventions

SUVN-502drug

Once-daily, tablets, orally

Placebodrug

Once-daily, tablets, orally

Donepezildrug

Donepezil HCl (10 mg, once a day)

Memantinedrug

Memantine HCl (10 mg, twice a day or 28 mg extended-release, once a day).