Inhaled Treprostinil (Tyvaso Nebulizer) For COPD Patients With Hypoxemia

PHASE1RecruitingINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

September 29, 2025

Primary Completion Date

July 1, 2027

Study Completion Date

July 1, 2027

Conditions
COPD (Chronic Obstructive Pulmonary Disease)Hypoxemia
Interventions
DRUG

Inhaled Treprostinil (Tyvaso Nebulizer)

Participants will receive inhaled Treprostinil (Tyvaso nebulizer), 6 µg per breath, administered four times daily for 4 weeks. The starting dose will be 3 breaths per session. The dose will increase by 1 breath per session each week, as tolerated, to a target of 6 breaths per session by week 4. If adverse effects occur, participants will remain at the highest tolerated dose. The drug will be administered using the Tyvaso inhalation system provided by United Therapeutics. No changes to baseline COPD maintenance medications are allowed during the treatment period. Participants will be monitored for safety throughout the study.

Trial Locations (1)

27705

RECRUITING

Duke Asthma Allergy and Airway Center, Durham

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

United Therapeutics

INDUSTRY

lead

Bastiaan Driehuys

OTHER

NCT07037836 - Inhaled Treprostinil (Tyvaso Nebulizer) For COPD Patients With Hypoxemia | Biotech Hunter | Biotech Hunter