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ACTIVE NOT RECRUITING Phase 3

Extension Study for Participants in LIQ861 Trials to Evaluate the Long-term Safety of Dry Powder Inhalation of Treprostinil

NCT03992755 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to evaluate the long-term safety of LIQ861 in patients with pulmonary arterial hypertension (PAH).

Interventions

  • DRUG LIQ861 Inhaled Treprostinil

Study Locations (20)

California

  • West Los Angeles VA Healthcare Center — Los Angeles
  • UC Davis Medical Center — Sacramento
  • Los Angeles Biomedical Research Center — Torrance

Florida

  • University of Florida — Gainesville
  • Mayo Clinic-Jacksonville — Jacksonville
  • AdventHealth — Orlando

Arizona

  • Banner University Medical Center — Phoenix
  • Arizona Pulmonary Specialists, Ltd. — Phoenix

Illinois

  • Northwestern Medicine, Feinberg School of Medicine — Chicago
  • University of Chicago Medicine — Chicago

Colorado

  • University of Colorado Anschutz Medical Campus — Aurora

Georgia

  • Emory University School of Medicine — Atlanta

Kansas

  • University of Kansas Medical Center — Kansas City

Louisiana

  • Ochsner Medical Center — New Orleans

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 2019-07-18
Est. Completion 2025-05-31
Phase Phase 3

Sponsor

Liquidia Technologies

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03992755

The ClinicalTrials.gov registry entry for NCT03992755 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 92 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Liquidia Technologies, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Primary Pulmonary Hypertension appearing as the primary indexed condition, and to 1 intervention — of which LIQ861 Inhaled Treprostinil is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03992755 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03992755 about?

NCT03992755 is a clinical study titled "Extension Study for Participants in LIQ861 Trials to Evaluate the Long-term Safety of Dry Powder Inhalation of Treprostinil". The primary objective of this study is to evaluate the long-term safety of LIQ861 in patients with pulmonary arterial hypertension (PAH).

What is the current status of trial NCT03992755?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 92 participants. The study started on 2019-07-18. Estimated completion is 2025-05-31.

What conditions does trial NCT03992755 study?

This clinical trial studies the following conditions: Primary Pulmonary Hypertension. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03992755?

The interventions under investigation include: LIQ861 Inhaled Treprostinil (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03992755?

This trial is sponsored by Liquidia Technologies, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03992755 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial