Last updated on February 2019

Trial to Evaluate Efficacy and Safety of Lenabasum in Diffuse Cutaneous Systemic Sclerosis


Brief description of study

This is a Phase 3 multicenter, double-blind, randomized, placebo-controlled study assessing the efficacy and safety of lenabasum for the treatment of diffuse cutaneous systemic sclerosis (SSc). Approximately 354 subjects will be enrolled in this study at about 60 sites in North America, Europe, Australia, and Asia. The planned duration of treatment with study drug is 52 weeks.

Clinical Study Identifier: NCT03398837

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Hospital for Special Surgery

New York, NY United States
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Liverpool Hospital

Liverpool, Australia
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UCLA

Los Angeles, CA United States
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Ninewells Hospital

Dundee, United Kingdom
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Pacific Arthritis Care Center

Los Angeles, CA United States
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Stanford University

Palo Alto, CA United States
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Cleveland Clinic

Cleveland, OH United States
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University of Toledo

Toledo, OH United States
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UTP Rheumatology Clinic

Houston, TX United States
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Tulane University Medical Center

New Orleans, LA United States
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Michigan Medicine

Ann Arbor, MI United States
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Recruitment Status: Open


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