Trial intelligence / Profile preview

Lucinactant for inhalation plus nCPAP in preterm neonates with respiratory distress syndrome

2015-003519-40Phase 2Completed

Sponsor
Windtree Therapeutics, Inc
Start
Jan 2016
Modality
Recombinant Proteins and Enzymes, Peptides
Countries
1
01

Overview

Phase 2, randomised, single-blind trial of lucinactant in respiratory distress syndrome (RDS) (2 arms), sponsored by Windtree Therapeutics, Inc. Primary endpoint: Time to respiratory failure or death due to respiratory distress syndrome within the first 72 hours of life. Started Jan 2016; status: completed.

02

Drugs

lucinactant
03

Conditions

respiratory distress syndrome (RDS)

Beyond the preview

Go deeper on 2015-003519-40.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on 2015-003519-40.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call