WithdrawnPhase 4NCT02882126
An Open Label Extension Study to Evaluate the Safety of Continued Therapy of Subcutanous Remodulin® in 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
- United Therapeutics
- Principal Investigator
- Junbo GeZhongshan Hospital affiliated with Fudan University
- Intervention
- Subcutaneous Treprostinil(drug)
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2021
Study locations (10)
- Beijing Chao-Yang Hospital, Beijing, China
- Beijing Anzhen Hospital, Capital Medical University, Beijing, China
- Peking Union Medical College Hospital, Beijing, China
- Fu Wai Hospital, Beijing, China
- Beijing Shijitan Hospital, Beijing, China
- Xiangya Hospital Centre South University, Changsha, China
- Guangdong General Hospital, Guangzhou, China
- Zhongshan Hospital affiliated with Fudan University, Shanghai, China
- Shanghai Pulmonary Hospital, Shanghai, China
- Wuhan Asia Heart Hospital, Wuhan, China
Collaborators
CVie Therapeutics Co. Ltd.
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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