RecruitingPhase 3NCT06350032
Investigational Trial to Evaluate Safety and Tolerability of Treprostinil in Children Diagnosed With PAH
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
- AOP Orphan Pharmaceuticals AG
- Intervention
- preservative-free parenteral treprostinil(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2028
Study locations (5)
- Medizinische Universität Wien, Vienna, Vienna, Austria
- Necker-Enfants Malades Hospital, Paris, Paris, Paris, France
- Gottsegen National Cardiovascular Center, Budapest, Budapest, Hungary
- Pediatric Cardiac Center, Bratislava, Slovakia
- Ramón y Cajal University Hospital, Madrid, Madrid, Spain
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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