CompletedPhase 3NCT01416636
Efficacy and Tolerability of Subcutaneously Administered Treprostinil Sodium in Patients With Severe (Non-operable) Chronic Thromboembolic Pulmonary Hypertension (CTREPH)
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
- SciPharm SàRL
- Principal Investigator
- Irene Lang, MDMedical University Vienna
- Intervention
- Treprostinil sodium(drug)
- Enrollment
- 105 enrolled
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2009 – 2021
Study locations (6)
- Krankenhaus der Elisabethinen, Linz, Austria
- Medical University of Vienna AKH - Division Cardiology, Vienna, Austria
- II. interní klinika Všeobecná fakultní nemocnice, Prague, Czechia
- Medical University Carl Gustav Carus Medizinische Klinik und Poliklinik I Medizinische Fakultät der Technischen Universität Dresden, Dresden, Germany
- Department of Cardiac and Vascular Diseases Centre for Rare Cardiovascular Diseases John Paul II Hospital, Krakow, Poland
- NZOZ Europejskie Centrum Zdrowia Otwock, Otwock, Poland
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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