CompletedPhase 2NCT02060721
Clinical Study to Assess the Safety, Tolerability and Efficacy of Macitentan in Subjects With Inoperable Chronic Thromboembolic Pulmonary Hypertension
Studying Chronic thromboembolic pulmonary hypertension
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Actelion
- Principal Investigator
- Erin McGuireActelion
- Intervention
- Macitentan(drug)
- Enrollment
- 76 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2022
Study locations (30)
- Leuven, Belgium
- Beijing, China
- Guangzhou, China
- Shanghai, China
- Shenyang, China
- Wuhan, China
- Prague, Czechia
- Le Kremlin-Bicêtre, France
- Paris, France
- Toulouse, France
- Giessen, Germany
- Heidelberg, Germany
- Würzburg, Germany
- Budapest, Hungary
- Debrecen, Hungary
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02060721 on ClinicalTrials.govOther trials for Chronic thromboembolic pulmonary hypertension
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