Phase 2 Clinical Trial of CartiLife® in the United States

PHASE2UnknownINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

October 28, 2020

Primary Completion Date

December 31, 2023

Study Completion Date

December 31, 2023

Conditions
Articular Cartilage DefectArticular Cartilage Degeneration
Interventions
DRUG

Autologous Chondrocyte Implantation (CartiLife®)

CartiLife consists of small beads (1 mm in diameter) in suspension, developed from pellet culture of autologous costal chondrocytes after multiplication. The beads are implanted in an injective manner with fibrin glue through minimal arthrotomy. The dose depends on the size (volume) of the defect, recommended dose is 480 pellets/cm\^3 defect

Trial Locations (5)

43210

RECRUITING

Ohio State University, Columbus

70506

RECRUITING

Lafayette General Health, Lafayette

91942

RECRUITING

Biosolutions Clinical Research Center, La Mesa

RECRUITING

Horizon Clinical Research, La Mesa

92612

NOT_YET_RECRUITING

Tilda Research, Irvine

Sponsors
All Listed Sponsors
lead

Biosolution Co., Ltd.

INDUSTRY