Inhaled Treprostinil in Participants With Pulmonary Hypertension Due to Chronic Obstructive Pulmonary Disease (PH-COPD)
| Condition | Pulmonary Hypertension, Chronic Obstructive Pulmonary Disease |
|---|---|
| Phase | Phase 3 |
| Sponsor | United Therapeutics |
| Status | Terminated |
| Enrollment | 41 participants |
| Interventions | Inhaled treprostinil solution |
| Start date | Dec 21, 2018 |
| Completion date | Nov 29, 2022 |
| Results posted | Dec 18, 2023 |
Summary
This open-label study will evaluate the safety of continued therapy with inhaled treprostinil in participants who have completed Study RIN-PH-304 (NCT03496623). This study hypothesizes that long-term safety findings will be similar to those observed in the randomized, placebo-controlled, double-blind, adaptive study 'A Phase 3, Randomized, Placebo-controlled, Double-blind, Adaptive Study to Evaluate the Safety and Efficacy of Inhaled Treprostinil in Patients with Pulmonary Hypertension due to Chronic Obstructive Pulmonary Disease (PH-COPD)(RIN-PH-304).
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)
| Treprostinil | 35 Participants |
|---|
Open in BENITIONS View on ClinicalTrials.gov
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- Efficacy of Fixed Combination of Beclometasone + Formoterol + Glycopyrrolate Versus Foster — Chiesi Farmaceutici S.p.A.
- Active Controlled Trial of CHF5993 Pressurized Metered-dose Inhaler ( pMDI) vs Symbicort®T — Chiesi Farmaceutici S.p.A.
- Tiotropium/Salmeterol Inhalation Powder in COPD — Boehringer Ingelheim
- Risk Factors, Costs, and Impacts of ED Boarding — University of Maryland, Baltimore
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