Clinical trials

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Condition / disease
Location
Status: Recruiting

A Phase 3 Study to Evaluate the Safety and Efficacy L606 in Participants With PH-ILD

The purpose of this study is to find out if L606 is safe and if it helps people with high blood pressure in the lungs (pulmonary hypertension) caused by interstitial lung disease (PH-ILD, WHO Group 3). One of the main ways the study will check this is by seeing if people can walk further in six minutes (called the "six-minute walk test"). Another important (secondary) goal is to see how long it takes for PH-ILD to get worse while people are taking L606. One way the study will measure this is by looking at the distance people walk at different times in the study on different doses of L606. Throughout the study, doctors will also closely monitor for any side effects people have to make sure L606 is safe. People who decide to join this study will be randomly (like tossing a coin) placed into one of two groups: one group will get L606 and the other group will get a placebo, which will look like L606 but will not contain any active medicine. At the end of the initial blinded portion of the study, study participants may have the opportunity to enroll in an open-label extension portion of the study where all participants will receive L606.

Participants needed: 344
Trial details
Phase: Phase 3Age: 18-80Biological sex: AllType: InterventionalSponsor: Liquidia Technologies, Inc.Updated: Jun 29, 2026Locations: 16
Eligibility criteria

Participant is between 18 years to 80 years old. [+6]

PH in the updated WHO Classification Groups 1, 2, 4, or 5. [+5]

Status: Recruiting

An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in PH

Study LTI-401 is an open-label, multicenter study which will evaluate the safety and tolerability of LIQ861 in subjects who have WHO Group 1 \& 3 PH.

Participants needed: 80
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Liquidia Technologies, Inc.Updated: Jun 26, 2026Locations: 23Duration: 52 Weeks
Eligibility criteria

Males or Females between 18 years to 80 years of age. [+4]

PH in the Updated WHO Classification Groups 1, 2, 4, or 5. [+15]