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Surfactant Replacement Therapy

Treatment for Respiratory Distress Syndrome

N/A
Waitlist Available
Research Sponsored by ONY
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

Surfactant replacement therapy can be life-saving for newborn infants born with symptomatic lung surfactant deficiency causing Respiratory Distress Syndrome (RDS). Currently, such therapy requires instillation of a liquid suspension into the trachea through an endotracheal tube. Endotracheal intubations have undesirable adverse effects on fragile premature infants. Instilling surfactant as a liquid suspension into the lung is associated with adverse events due to interruption of breathing in patients who already have respiratory insufficiency. This treatment protocol is expanded access that offers the opportunity for patients to receive aerosolized Infasurf prior to FDA acting on ONY Biotech's application for approval for commercial marketing of aerosolized Infasurf.

Eligible Conditions
  • Respiratory Distress Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

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Who is running the clinical trial?

ONYLead Sponsor
8 Previous Clinical Trials
1,384 Total Patients Enrolled
6 Trials studying Respiratory Distress Syndrome
1,316 Patients Enrolled for Respiratory Distress Syndrome
Jim Cummings, MDStudy ChairAlbany Medical College
1 Previous Clinical Trials
220 Total Patients Enrolled
1 Trials studying Respiratory Distress Syndrome
220 Patients Enrolled for Respiratory Distress Syndrome
~233 spots leftby Sep 2025