CompletedPhase 2NCT04266197

Vardenafil Inhaled for Pulmonary Arterial Hypertension PRN Phase 2B Study

Studying Drug- or toxin-induced pulmonary arterial hypertension

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
Respira Therapeutics, Inc.
Principal Investigator
Ed Parsley, DO
Respira Therapeutics
Intervention
Drug: RT234 - vardenafil inhalation powder; Device: Axially Oscillating Sphere dry powder inhaler (AOS DPI)(combination_product)
Enrollment
42 enrolled
Eligibility
18-80 years · All sexes
Timeline
20202025

Study locations (26)

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.

Open NCT04266197 on ClinicalTrials.gov

Other trials for Drug- or toxin-induced pulmonary arterial hypertension

Additional recruiting or active studies for the same condition.

See all trials for Drug- or toxin-induced pulmonary arterial hypertension

← Back to all trials