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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 Oct 24, 2026, 6:45 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)

Brief summary

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

This 6-month extension study will provide further information regarding the long-term safety and tolerability of intepirdine (RVT-101) in subjects with Dementia with Lewy bodies (DLB) who have participated in the double-blind, placebo-controlled, lead-in study RVT-101-2001.

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

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
Oct 2016 (Actual)
Primary completion
Feb 2018 (Actual)
Completion
Feb 2018 (Actual)
Last update posted
Apr 18, 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 18, 2018 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02928445 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →