CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 484 enrolled
Drug / intervention
RVT-101 35 mg +2 moredrug
Likely dose
RVT-101 35 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/NCT02669433
NCT02669433Phase 2Completed

A Phase 2b, Double-Blind, Randomized, Placebo-Controlled Study of RVT-101 in Subjects With Dementia With Lewy Bodies (DLB)

Axovant Sciences Ltd.·interventional·Posted Feb 1, 2016·Updated Apr 26, 2019

In Brief

A Phase 2 clinical trial evaluating RVT-101 35 mg, RVT-101 70 mg, and 1 other intervention for Dementia With Lewy Bodies. Completed, enrolled 484 participants across 65 sites in 7 countries.

Detailed Summary

This study seeks to evaluate the efficacy and safety of intepirdine (RVT-101) in patients with dementia with Lewy bodies.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Italy, Netherlands, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 1, 2016
Enrollment StartJan 1, 2016
Primary CompletionDec 1, 2017
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 10.4 years ago

Interventions

RVT-101 35 mgdrug

once daily, oral, 35-mg tablets

RVT-101 70 mgdrug

once daily, oral, 35-mg tablets

Placebodrug

once daily, oral, matching tablets