This study seeks to evaluate the long-term safety and effectiveness of nelotanserin for the
treatment of visual hallucinations (VHs) and Rapid Eye Movement (REM) Sleep Behavior Disorder
(RBD) in subjects with Lewy body dementia (LBD).
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02871427
Ages eligible for Study
50 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Subjects with LBD who completed a previous nelotanserin VH or RBD study
Subjects with a current serious and/or unstable cardiovascular, respiratory, thyroid, gastrointestinal, renal, hematologic or other medical disorder
All locations for NCT02871427
United States (19)
Birmingham, Alabama, United States, 35294
Little Rock, Arkansas, United States, 77205
Boca Raton, Florida, United States, 33486
Maitland, Florida, United States, 32751
Ocala, Florida, United States, 34471
Orlando, Florida, United States, 32806
Ormond Beach, Florida, United States, 32174
Indianapolis, Indiana, United States, 46202
Lenexa, Kansas, United States, 66214
Rochester, Minnesota, United States, 55905
Lincoln, Nebraska, United States, 68526
Chapel Hill, North Carolina, United States, 27514
Fargo, North Dakota, United States, 58103
Cincinnati Children's Hospital
Cincinnati, Ohio, United States, 45229
Columbus, Ohio, United States, 43210
Lincoln, Rhode Island, United States, 02865
Memphis, Tennessee, United States, 38163
San Antonio, Texas, United States, 78229
Cleveland, Ohio, United States, 44195
View full eligibility
Tris trial is registered with FDA with number: NCT02871427. The sponsor of the trial is Axovant Sciences Ltd. and it is looking for 80 volunteers for the current phase.
Official trial title: An Open-label Study of Nelotanserin in Patients With Lewy Body Dementia Who Have Frequent Visual Hallucinations or REM Sleep Behavior Disorder
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