Long-term Safety and Efficacy Follow-up Study of PNEUMOSTEM® in Patients Who Completed PNEUMOSTEM® Phase-I Study

CompletedOBSERVATIONAL
Enrollment

8

Participants

Timeline

Start Date

April 30, 2014

Primary Completion Date

October 31, 2016

Study Completion Date

October 31, 2016

Conditions
Bronchopulmonary DysplasiaRespiratory Tract InfectionsPremature Birth of Newborn
Interventions
BIOLOGICAL

PNEUMOSTEM

"A single intratracheal administration~Low Dose Group (3 patients): 1.0 x 10\^7 cells/kg High Dose Group (6 patients): 2.0 x 10\^7 cells/kg~\* The subjects were administered with Pneumostem in the earlier part of the Phase I study. No drug/biologics will be administered to any subject during this part of the study."

Trial Locations (1)

Unknown

Samsung Medical Center, Seoul

All Listed Sponsors
lead

Medipost Co Ltd.

INDUSTRY

NCT02023788 - Long-term Safety and Efficacy Follow-up Study of PNEUMOSTEM® in Patients Who Completed PNEUMOSTEM® Phase-I Study | Biotech Hunter | Biotech Hunter