drugset / Trial / NCT02260557

Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis

NCT02260557 ↗

Phase 2 Completed 74 enrolled Actelion
RandomizedParallel-groupQuadruple-blindTreatment

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).

Timeline

Start
2014-10-31
Primary completion
2015-04-30
Completion
2015-06-30

Outcome

Missed primary endpoint

paper Treatment with selexipag did not reduce the number of RP attacks compared with placebo. PMID 29193819 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Selexipag Small molecule 200 ug Oral

Indications