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Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil

Completed · Phase 3 · NCT03399604

Conditions: Primary Pulmonary Hypertension

At a glance

Research payments reported, 2025
$58,113
U.S. investigators named
7
Sites paid
7
Planned or actual enrollment
121

About the trial

Sponsor
Liquidia Technologies, Inc. (with Nuventra, Inc.)
Tested
LIQ861 Inhaled Treprostinil (drug)
Dates
Started 2018-01-02; completion 2019-11-25
Results posted
Yes

The primary objective of this study is to evaluate the long-term safety and tolerability of LIQ861, a dry powder formulation of treprostinil, in patients with Pulmonary Arterial Hypertension (PAH).

From ClinicalTrials.gov, last updated 2024-07-30. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Liquidia Technologies, Inc. reported $58,113 in research payments for this study in 2025 (38 payments).

Products named: Yutrepia

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.