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An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in PH
NCT06129240 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG LIQ861
Study Locations (18)
California
- The Medical Research Group, Inc. — Fresno
- UCLA Westwood — Los Angeles
- UC Davis — Sacramento
- UCSF — San Francisco
Florida
- Advent Health — Orlando
- Tampa General Hospital Center of Research Excellence — Tampa
New York
- NYU Langone Medical Center — New York
- University of Rochester — Rochester
Arizona
- Arizona Pulmonary Specialists — Phoenix
Colorado
- National Jewish Health — Denver
Indiana
- Vincent Medical Group — Indianapolis
Michigan
- University of Michigan — Ann Arbor
Minnesota
- University of Minnesota — Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2023-12-28 |
| Est. Completion | 2028-02-08 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06129240
The ClinicalTrials.gov registry entry for NCT06129240 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 80 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 2 conditions, with Pulmonary Hypertension appearing as the primary indexed condition, and to 1 intervention — of which LIQ861 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: NCT06129240 reports 18 study locations spanning 13 distinct geographic areas — top geographies include California, Florida, New York. 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 NCT06129240 about?
NCT06129240 is a clinical study titled "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.
What is the current status of trial NCT06129240?
This trial is currently active not recruiting. The enrollment target is 80 participants. The study started on 2023-12-28. Estimated completion is 2028-02-08.
What conditions does trial NCT06129240 study?
This clinical trial studies the following conditions: Pulmonary Hypertension, Interstitial Lung Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06129240?
The interventions under investigation include: LIQ861 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06129240?
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 NCT06129240 being conducted?
This trial has 18 study locations across Arizona, California, Colorado, Florida, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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