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Terminated Phase 2Phase 3 Interventional

Long-Term Extension Study of Intepirdine (RVT-101) in Subjects With Dementia With Lewy Bodies: HEADWAY-DLB Extension

ClinicalTrials.gov ID: NCT02928445

Public ClinicalTrials.gov record NCT02928445. 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 Jul 24, 2026, 12:44 AM 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 Long-Term Extension Study of the Safety and Tolerability of RVT-101 in Subjects With Dementia With Lewy Bodies (DLB)

Study identification

NCT ID
NCT02928445
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Axovant Sciences Ltd.
Industry
Enrollment
240 participants

Conditions and interventions

Interventions

  • RVT-101 35 mg Drug
  • RVT-101 70 mg Drug

Drug

Eligibility (public fields only)

Age range
50 Years to 86 Years
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
Sep 30, 2016
Primary completion
Jan 31, 2018
Completion
Jan 31, 2018
Last update posted
Apr 17, 2018

2016 – 2018

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
26
Facility City State ZIP Site status
US138 Phoenix Arizona 85006
US108 Phoenix Arizona 85013
US139 Sun City Arizona 85351
US125 Tucson Arizona 85704
US119 Orange California 92868
US134 Oxnard California 93030
US133 Rancho Mirage California 92270
US140 Sacramento California 95816
US141 Englewood Colorado 80113
US123 Washington D.C. District of Columbia 20007
US104 Boca Raton Florida 33431
US111 Jacksonville Florida 32224
US122 Orlando Florida 32806
US137 Palm Beach Gardens Florida 33410
US126 Tampa Florida 33609
US136 Atlanta Georgia 30331
US118 Indianapolis Indiana 46202
US105 Lexington Kentucky 40536
US130 Quincy Massachusetts 02196
US102 Rochester Minnesota 55905
US109 New York New York 10032
US100 Chapel Hill North Carolina 27514
US110 Cleveland Ohio 44195
US106 Columbus Ohio 43210
US131 Portland Oregon 97210
US120 Willow Grove Pennsylvania 19090
US101 Charlottesville Virginia 22908

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02928445, 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 Apr 17, 2018 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02928445 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →