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Brief Title: Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis
Official Title: A Multi-center, Double-blind, Randomized, Placebo-controlled, Parallel Group, Exploratory Phase 2 Study to Assess Efficacy and Safety of Selexipag in Adult Subjects With Raynaud's Phenomenon Secondary to Systemic Sclerosis
Study ID: NCT02260557
Brief Summary: The primary objective of the study is to determine the activity of selexipag on Raynaud attack frequency in subjects with Raynaud's Phenomenon (RP) secondary to Systemic Sclerosis (SSc).
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Investigator Site, Grenoble cedex, , France
Investigator Site, Lille Cedex, , France
Investigator Site, Nantes Cedex 1, , France
Investigator Site, Paris, , France
Investigator Site, Strasbourg, , France
Investigator Site, Bad Nauheim, , Germany
Investigator Site, Berlin, , Germany
Investigator Site, Erlangen, , Germany
Investigator Site, Koln, , Germany
Investigator Site, Magdeburg, , Germany
Investigator Site, Mainz, , Germany
Investigator Site, Bath, , United Kingdom
Investigator Site, Leeds, , United Kingdom
Investigator Site, Liverpool, , United Kingdom
Investigator Site, London, , United Kingdom
Investigator Site, Salford, , United Kingdom
Name: Ralph Preiss, MD
Affiliation: Actelion
Role: STUDY_CHAIR