CompletedPhase 1NCT05948644
The Safety, Tolerability, and Pharmacokinetics of TPN171H Tablets in Patients With 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
- Vigonvita Life Sciences
- Principal Investigator
- Fu ZhuShanghai Xuhui Central Hospital
- Intervention
- TPN171H(drug)
- Enrollment
- 10 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2019 – 2020
Study locations (1)
- Fu Zhu, Shanghai, China
Collaborators
Shanghai Institute of Materia Medica, Chinese Academy of Sciences
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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