A Study of Inhaled Treprostinil (LIQ861) in Adults With Pulmonary Arterial Hypertension Transitioning From Oral Selexipag
Part of paid clinical trials in Columbus, Georgia.
- Sponsor
- Liquidia Technologies, Inc.
- Study ID
- NCT07759804
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
- Pulmonary Arterial Hypertension (PAH)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- LIQ861 (treprostinil) inhalation powder — COMBINATION_PRODUCTTreprostinil inhalation powder supplied in capsules for oral inhalation using a handheld, single-capsule dry powder inhaler. Participants self-administer study drug four times daily (QID), and titrated on tolerability and symptom relief.
Study Details
This study will look at safety and tolerability of LIQ861 (treprostinil) inhalation powder in adults with pulmonary arterial hypertension (PAH, WHO Group 1) who switch from selexipag, a medicine taken by mouth, to treprostinil, a medicine breathed into the lungs. Everyone who takes part will receive LIQ861. On the first study day, participants will stop taking selexipag and begin taking LIQ861 four times a day using a small handheld dry powder inhaler. The dose may be increased over time based on how well it is tolerated. Participants will take LIQ861 for 16 weeks. The study will also look at whether switching to LIQ861 affects walking distance, a blood marker of heart strain, and symptoms reported by participants.
Key Dates
- First listed
- Aug 12, 2026
- Start date
- Sep 30, 2026
- Status verified
- Aug 2026
- Primary completion
- May 31, 2027
- Completion
- Jun 30, 2027
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Selexipag to LIQ861 (treprostinil) inhalation powder
Primary Outcome Measure
Treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) [ Time Frame: Day 1 through 30 days after the last dose of study drug (up to approximately 24 weeks) ]
Central Contacts
- Liquidia Point of Contact1-888-241-6906
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Southeastern Cardiology Associates | Columbus | Georgia | 31904 |
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