Study Phase 4

A Multi-center, Double-blind, Placebo-controlled Phase 4 Study in Patients With Pulmonary Arterial Hypertension to Assess the Effect of Selexipag on Daily Life Physical Activity and Patient's Self-reported Symptoms and Their Impacts

Trial Information

Generic NameSelexipagProduct NameUPTRAVI®Therapeutic AreaRespiratory Tract (Lung and Bronchial) DiseasesEnrollment108% Female71.3%% White88.9%
Product ClassProstacyclin receptor agonistSponsor Protocol NumberAC-065A404Data PartnerJohnson & JohnsonCondition StudiedArterial, Hypertension, PulmonaryMean/Median Age (Years)49.4

Supporting Documentation

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

Approved Data Requests Associated with this Trial

Disclaimer

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