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Hemodynamic Evaluation of Dose-response and Safety of Dry Powder Inhalation of Treprostinil

Pulmonary Arterial Hypertension Clinical Trial

Official title:
A Two Part, Phase 2 Open-label, Multi-Centre, Dose Escalation Hemodynamic Study to Evaluate Dose-Response and Safety of Inhaled LIQ861 (Treprostinil) in Pulmonary Arterial Hypertension (WHO Group 1) Subjects

Clinical Trial Summary

Acute and chronic hemodynamic dose-response and safety evaluation of LIQ861 in PAH subjects.

Clinical Trial Description

Data will be collected on acute and chronic hemodynamic response to inhaled dry powder treprostinil (LIQ861) via right-heart catheterization. Study subjects will contribute to the overall safety profile of LIQ861. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03884465
Study type Interventional
Source Liquidia Technologies, Inc.
Contact
Status Terminated
Phase Phase 2
Start date November 11, 2019
Completion date December 23, 2020
View Details
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