← Eichor
Study identifier: NCT05960929 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

InfasurfAero™ Versus Sham Treatment in Preterm Newborns With RDS

Condition: Respiratory Distress Syndrome (Neonatal) · Intubation Complication · Death; Neonatal  ·  Sponsor: ONY

PhasePhase 3
Planned participants220
Who can joinAll sexes, 29 Weeks to 36 Weeks
Healthy volunteersNo

About this study

The purpose of this clinical study is to determine the effectiveness and safety of Infasurf® administered through the InfasurfAero™, a novel oral airway delivery device specifically designed to give Infasurf in a less complicated way and without the need for a breathing tube or interrupting nasal respiratory support.

This description comes directly from the study's public registry record.

Talk to the study team

Corey Commaroto, RRT  ·  7163614659  ·  ccommaroto@onybiotech.com

Dan Swartz, PhD  ·  716428-3132  ·  dswartz@onybiotech.com

Always discuss trial participation with your own doctor first.

Locations (10)

St. Josephs Hospital and Medical CenterPhoenix, Arizona, United StatesRecruiting
Phoenix Children'sPhoenix, Arizona, United StatesRecruiting
Sharp Mary Birch Hospital for Women & NewbornsSan Diego, California, United StatesRecruiting
University of Florida -JacksonvilleJacksonville, Florida, United StatesRecruiting
Kapi'olani Medical Center for Women & ChildrenHonolulu, Hawaii, United StatesRecruiting
Jersey Shore University Medical CenterNeptune City, New Jersey, United StatesRecruiting
Sisters of Charity HospitalBuffalo, New York, United StatesRecruiting
Western TN- Jackson-Madison County General HospitalJackson, Tennessee, United StatesRecruiting
Utah Valley HospitalProvo, Utah, United StatesRecruiting
Unity Point MeriterMadison, Wisconsin, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05960929