Clinical Trial to Evaluate Efficacy and Safety of JOINTSTEM in Patients With Degenerative Arthritis

Biostar Stem Cell Research Institute (R-Bio)

Status and phase

Completed

Phase 2

Conditions

Degenerative Arthritis

Knee Osteoarthritis

Treatments

Biological: JOINTSTEM

Drug: Saline solution

Study type

Interventional

Funder types

Industry

Identifiers

NCT02658344

Jointstem2b

Details and patient eligibility

About

The purpose of this study is to investigate the efficacy and safety of autologous transplantation of Adipose Tissue derived Mesenchymal stem cells (MSCs) in patient with Knee Osteoarthritis.

Full description

JOINTSTEM is an OA treatment that uses autologous adipose-derived mesenchymal stem cells. As it does not use allogenic tissues and is incubated without additional genetic modification or mechanical and chemical modification through differentiation, it is classified as 'autologous cell therapy' and is completely free of immunologic rejection.

It primarily aims to improve pain and joint function, and secondary, to regenerate cartilage. The intra-articular injection of JOINTSTEM is expected to stimulate the regeneration and growth of cartilage, and to innovatively improve pain and joint function with cartilage regeneration within six months.

The subjects of this therapy were regenerative patients with K&L grade 2~4 aged 18 or older. JOINTSTEM is expected to be used in patients who have significantly damage cartilage due to its cartilage regeneration ability, in addition to its improvement of pain and joint performance. A;sp. Patients who had already undergone knee arthroplasty can delay their additional surgery with the use of JOINTSTEM. For dose who still have their own cartilage, arthroplasty is not an immediate treatment option, and osteoporosis patients who cannot undergo arthroplasty due to their advanced age can receive JOINTSTEM.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18 and older, male and female
Patients must consent in writing to participate in the study by signing and dating an informed consent document
Diagnosis of osteoarthritis by ACR osteoarthritis of the knee
Diagnosis of osteoarthritis by radiographic criteria of Kellgren and Lawrence grade 2-4
More than Grade 4 (0~10 point numeric scale) pain at least for 12 weeks
Diagnosis of osteoarthritis of class Ⅰ~Ⅲ by ACR(American College of Rheumatology Criteria) Global functional criteria
Patient who agree with contraception

Exclusion criteria

Preparing for Pregnancy or Pregnant women or lactating mothers.
Patients with Body Mass Index (BMI) > 35.
Patients with other disease including

: Septic arthritis, Rheumatoid or Inflammatory joint disease, Crystalline disease (gout or pseudogout), Paget disease, Articular fractures, Ochronosis, Acromegaly, Hemochromatosis, Wilson's disease, Osteochondromatosis, Hereditary disorder
Patients with serious condition internal medicine disease
Patients with positive human immunodeficiency (HIV), hepatitis B (HBV), hepatitis C (HCV), syphilis at screening indicative of current of pass infection.
Patient with behavioral disorders, cognitive disorders and chronic mental symptoms
Patient with significant neurologic or psychiatric disorders
Patients who alcohol, drug abuse history
Patients who had participated in other clinical trials within 12 weeks prior to this study.
Patients who received any drug by intra-articular injection for treatment within 2 months prior to this enrollment.
Patients who experienced as the knee joint cartilage and stem cell therapy
Patients who the principal investigator considers inappropriate for the clinical trial due to any other reasons than those listed above
Patients who penicillin hypersensitivity reactions -