CompletedPhase 2NCT05343637
A Dose Escalation Study to Evaluate the Effect of RT234 in Subjects 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
- Respira Therapeutics, Inc.
- Principal Investigator
- Carol Ann Satler, MD, PhDRespira Therapeutics
- Intervention
- Drug: RT234 - vardenafil inhalation powder; Device: RS01 dry powder inhaler (RS01 DPI)(combination_product)
- Enrollment
- 14 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2019 – 2020
Study locations (3)
- St Vincent's Hospital, Darlinghurst, New South Wales, Australia
- Royal Hobart Hospital, Hobart, Tasmania, Australia
- The Alfred Hospital, Melbourne, Victoria, Australia
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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