Last updated on September 2017

Study to Assess the Efficacy and Safety of Raxone in LHON Patients


Brief description of study

LEROS is an open-label interventional Phase IV study, designed to further assess the efficacy and safety of Raxone® in the long-term treatment of LHON patients.

Clinical Study Identifier: NCT02774005

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Derek Kunimoto, MD

Retinal Consultants of Arizona
Phoenix, AZ United States
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Levin Marc, MD

Palo Alto Medical Foundation
Palo Alto, CA United States
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Joyce Liao, MD

Stanford Byers Eye Institute
Stanford, CA United States
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Prem Subramanian, MD

University of Colorado Health Eye Center
Aurora, CO United States
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Nancy Newman, MD

Emory University Hospital
Atlanta, GA United States
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David Katz, MD

Bethesda Neurology, LLC
Bethesda, MD United States
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Gregory Van Stavern, MD

Washington University
Saint Louis, MO United States
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Rudrani Banik, MD

New York Eye and Ear Infirmary
New York, NY United States
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Steven Newman, MD

University of Virginia
Charlottesville, VA United States
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Vanessa Ferreira

AKH - Medizinische Universitaet Wien
Wien, Austria
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Vanessa Ferreira

CHU Saint-Pierre
Brussels, Belgium
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Vanessa Ferreira

Cliniques Universitaire Saint-Luc
Brussels, Belgium
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Vanessa Ferreira

Universitair Ziekenhuis Gent
Gent, Belgium
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Vanessa Ferreira

UZ Leuven - Campus Sint-Rafa l
Leuven, Belgium
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Vanessa Ferreira

C. H. U. Sart Tilman
Liège, Belgium
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Vanessa Ferreira

Military Medical Academy - MHAT - Pleven
Pleven, Bulgaria
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Vanessa Ferreira

UMHAT "Alexandrovska" EAD
Sofia, Bulgaria
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Vanessa Ferreira

Friedrich-Baur-Institut
Muenchen, Germany
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Vanessa Ferreira

Universit di Bologna-Clinica Neurologica-Dipartimento di Scienze Neurologiche
Bologna, Italy
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Bozena Romanowska-Dixon, MD

SPZOZ Spital Uniwersytecki w Krakowie, Oddzial Kliniczny Okulistyki i Onkologii Okulistycznej
Krakow, Poland
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Wojciech Lubinski, MD

Samodzielny Publiczny Szpital Kliniczny Nr 2 PUM w Szczecinie
Szczecin, Poland
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Jacek Szaflik, MD

Samodzielny Publiczny Kliniczny Szpital Okulistyczny
Warszawa, Poland
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