drugset / Trial / NCT03389321

Clinical Study to Investigate Effect of Macitentan on Riociguat Pharmacokinetics

NCT03389321

Phase 1 Completed 20 enrolled Actelion
NaSingle-groupOpen-labelOther

Summary

Both macitentan and riociguat are indicated in the treatment of pulmonary arterial hypertension (PAH) and may be administered concomitantly. The primary objective of this study is to evaluate the effect of macitentan administered for 11 days on the pharmacokinetics (PK) (i.e., amount and time of presence in the blood of riociguat) of a single dose of riociguat in healthy male subjects.

Timeline

Start
2018-01-09
Primary completion
2018-02-06
Completion
2018-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Macitentan Other / unclassified 10 mg Oral
Subject Riociguat Other / unclassified 1 mg Oral

Indications

No indication recorded.