Efficacy and Safety Evaluation of Pneumostem® Versus a Control Group for Treatment of BPD in Premature Infants

Medipost

Status and phase

Completed

Phase 2

Conditions

Bronchopulmonary Dysplasia

Treatments

Biological: Pneumostem®

Other: Normal Saline

Study type

Interventional

Funder types

Industry

Identifiers

NCT01828957

MP-CR-009

Details and patient eligibility

About

The objective of this study is to evaluate the efficacy and safety of a single intratracheal administration of Pneumostem® for treatment of Bronchopulmonary Dysplasia (BPD) in high-risk premature infants by comparing Pneumostem-treated group with a control group.

Enrollment

69 patients

Sex

All

Ages

5 to 14 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age: 5 - 14 days since birth
Fetal gestational age: ≥23 weeks and <29 weeks
Birth weight: ≥500g and ≤1250g
Premature infant of equal to or less than 2 weeks of age who is receiving a ventilator therapy at a rate of > 12 breath/min and > 25% oxygen
Patient whose ventilator setting has not been changed and who has shown aggravation of the illness within the 24 hours prior to the study enrollment
Patient with a written consent form signed by a legal representative or a parent upon explanation of the clinical trial

Exclusion criteria

Patient with concurrent cyanotic or acyanotic congenital heart diseases, except for patent ductus arteriosus
Patient with a concurrent severe lung malformation (i.e. Pulmonary hypoplasia, congenital diaphragmatic hernia, congenital cystic lung disease)
Patient with a concurrent severe lung malformation with chromosome anomalies (i.e. Edward syndrome, Patau syndrome, Down syndrome, etc) or severe congenital malformation (Hydrocephalus, Encephalocele, etc)
Patient with a concurrent severe congenital infection (i.e. Herpes, Toxoplasmosis, Rubella, Syphilis, AIDS, etc)
Patient withCRP > 30 mg/dL; Severe sepsis or shock
Patient who is scheduled for or expected to undergo a surgical procedure 72 hours prior to/following the administration of the study drug
Patient who has been administered with a surfactant within the 24 hours prior to the administration of the study drug
Patient with severe intracranial hemorrhage ≥ grade 3 or 4
Patient with active pulmonary hemorrhage or active air leak syndrome at the time of screening
Patient with a history of participating in other clinical studies
Patient who is allergic to Gentamicin
Patient who is considered inappropriate to participate in the study by the investigator