Active, not recruitingPhase 3NCT04691154

A Phase 3 Study to Evaluate the Safety and Tolerability of L606 in Subjects With PAH or PH-ILD

Studying Heritable pulmonary arterial hypertension

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Key facts

Sponsor
Liquidia Technologies, Inc.
Intervention
L606 inhalation suspension(combination_product)
Enrollment
28 enrolled
Eligibility
18-80 years · All sexes
Timeline
20212031

Study locations (8)

Collaborators

PPD Development, LP

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT04691154 on ClinicalTrials.gov

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