Follow-Up Study of Safety and Efficacy of Pneumostem® in Premature Infants With Bronchopulmonary Dysplasia

Active, not recruitingOBSERVATIONAL
Enrollment

9

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

September 30, 2025

Study Completion Date

September 30, 2026

Conditions
Bronchopulmonary Dysplasia
Interventions
BIOLOGICAL

Pneumostem®

"A single intratracheal administration~Low Dose Group (3 patients): 1.0 x 10\^7 cells/kg, High Dose Group (6 patients): 2 x 10\^7 cells/kg~\* The subjects were administered with Pneumostem® in the earlier part of the phase I study. No drugs/biologics are administered during this part of the study."

Trial Locations (2)

135-710

Samsung Medical Center, Seoul

Unknown

Samsung Medical Center, Seoul

All Listed Sponsors
collaborator

Medipost Co Ltd.

INDUSTRY

lead

Samsung Medical Center

OTHER

NCT01632475 - Follow-Up Study of Safety and Efficacy of Pneumostem® in Premature Infants With Bronchopulmonary Dysplasia | Biotech Hunter | Biotech Hunter