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Terminated Phase 2 Interventional Results available

Trial To Assess The Safety And Tolerability Of Lucinactant For Inhalation In Preterm Neonates 26 to 28 Weeks PMA

ClinicalTrials.gov ID: NCT02528318

Public ClinicalTrials.gov record NCT02528318. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 12:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Open-label, Controlled Trial To Assess The Safety And Tolerability Of Lucinactant For Inhalation In Preterm Neonates 26 to 28 Weeks PMA

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is to evaluate the safety and tolerability of lucinactant for inhalation, administered as an aerosol in up to four escalating doses to preterm neonates 26 to 28 weeks gestational age who are receiving nCPAP for RDS compared to neonates receiving nCPAP alone.

Study identification

NCT ID
NCT02528318
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Windtree Therapeutics
Industry
Enrollment
48 participants

Conditions and interventions

Interventions

Combination Product · Device

Eligibility (public fields only)

Age range
26 Weeks to 28 Weeks
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2015 (Actual)
Primary completion
May 31, 2017 (Actual)
Completion
Aug 11, 2017 (Actual)
Last update posted
Jul 23, 2019

2015 – 2017

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Loma Linda University Medical Center Loma Linda California 92354 —
Sharp Mary Birch Hospital for Women and Newborns San Diego California 92123 —
Christiana Care Health System Newark Delaware 19713 —
University of Miami Miami Florida 33136 —
University of Louisville Louisville Kentucky 40202 —
University of Nebraska Medical Center Omaha Nebraska 68105 —
Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital - Morgan Stanley Children's Hospital New York New York 10032 —
New Hanover Regional Medical Center Wilmington North Carolina 28401 —
Providence St. Vincent Medical Center Portland Oregon 97225 —
Women and Infants Hospital Providence Rhode Island 02905 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02528318, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 23, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02528318 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →