Study Phase 2

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

Trial Information

Generic NameSelexipagProduct NameUPTRAVI®Therapeutic AreaRespiratory Tract (Lung and Bronchial) DiseasesEnrollment74% Female81.1%% White93.2%
Product ClassProstacyclin receptor agonistSponsor Protocol NumberAC-065C202Data PartnerJohnson & JohnsonCondition StudiedScleroderma, SystemicMean/Median Age (Years)52.6

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Protocol with Amendments Available
  • Statistical Analysis Plan Available
  • Clinical Study Report Available

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