CompletedPhase 3NCT03187678
Safety Study of the Switch From Oral Selexipag to Intravenous Selexipag in Subjects With Stable Pulmonary Arterial Hypertension
Studying Drug- or toxin-induced pulmonary arterial 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
- Ralph PreissActelion
- Intervention
- i.v. selexipag(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2017 – 2018
Study locations (8)
- University of California San Diego Medical center - PULM VASCULAR DIV, La Jolla, California, United States
- TUFTS New England Medical Center - PULM / CRITICAL CARE & SLEEP, Boston, Massachusetts, United States
- Cleveland Clin Foundation - Dept of Pulm & Critical Care Med, Cleveland, Ohio, United States
- University of Texas Southwestern Medical Center, Dallas, Texas, United States
- Universitätsklinikum Giessen und Marburg GmbH, Medizinische Klinik und Poliklinik II, Pneumologie, Giessen, Germany
- Universitätsmedizin Greifswald, Klinik und Poliklinik für Innere Medizin B, Greifswald, Germany
- Universitätsklinikum Hamburg-Eppendorf, II. Medizinische Klinik und Poliklinik, Pneumologie, Hamburg, Germany
- Universitätsklinikum Leipzig / Medizinischen Klinik und Poliklinik I, Pneumologie, Leipzig, Germany
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.
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