Clin2
NCT06129240Possibly a fitRecruiting

Study of a new inhaled treprostinil powder for PH-ILD

Pulmonary HypertensionInterstitial Lung Disease

Part of Heart & circulation, Lungs & breathing clinical trials.

This study tests a new dry powder inhaled medicine called LIQ861 for people with pulmonary hypertension related to lung scarring (PH-ILD). If you are already taking an inhaled treprostinil treatment but need better control, this trial may help you switch to a potentially easier-to-use version.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
80 people
Ages
18 years to 80 years
Study type
Observational

Who can take part

  • You must be between 18 and 75 years old.
  • You need a confirmed diagnosis of pulmonary hypertension caused by lung scarring (PH-ILD).
  • You must have had a right heart catheterization showing high pressure in your lung arteries.
  • You must be able to walk at least 200 meters (about 2 city blocks) in 6 minutes.
  • You must currently be taking an inhaled treprostinil medicine (like Tyvaso) and be ready to switch to the study drug LIQ861.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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