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Completed Phase 2 Interventional Results available

Study Evaluating Nelotanserin for Treatment of REM Sleep Behavior Disorder in Subjects With Dementia (DLB or PDD)

ClinicalTrials.gov ID: NCT02708186

Public ClinicalTrials.gov record NCT02708186. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 6:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Double-blind, Randomized, Placebo-controlled Study of Nelotanserin Versus Placebo in Subjects With Dementia With Lewy Bodies (DLB) or Parkinson's Disease Dementia (PDD) Who Have REM Sleep Behavior Disorder (RBD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study seeks to evaluate the safety and efficacy of Nelotanserin for the treatment of Rapid Eye Movement (REM) Sleep Behavior Disorder (RBD) in subjects with dementia with Lewy bodies (DLB) or Parkinson's disease dementia (PDD).

Study identification

NCT ID
NCT02708186
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Axovant Sciences Ltd.
Industry
Enrollment
34 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2016 (Actual)
Primary completion
May 2018 (Actual)
Completion
May 2018 (Actual)
Last update posted
May 20, 2020

2016 – 2018

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
US120 Birmingham Alabama 35294 —
US164 Phoenix Arizona 85013 —
US145 Sun City Arizona 85351 —
US143 Little Rock Arkansas 72205 —
US122 Englewood Colorado 80113 —
US180 Maitland Florida 32751 —
US154 Ocala Florida 34471 —
US113 Orlando Florida 32806 —
US152 Ormond Beach Florida 32174 —
US153 Tampa Florida 33613 —
US163 Atlanta Georgia 30331 —
US107 Indianapolis Indiana 46202 —
US132 Lenexa Kansas 66214 —
US129 Lincoln Nebraska 68526 —
US101 Chapel Hill North Carolina 27514 —
US159 New Bern North Carolina 28562 —
US147 Fargo North Dakota 58103 —
US111 Cincinnati Ohio 45229 —
US104 Cleveland Ohio 44195 —
US105 Columbus Ohio 43210 —
US173 Lincoln Rhode Island 02865 —
US128 Memphis Tennessee 38613 —
US131 San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02708186, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 20, 2020 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02708186 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →