Efficacy and Safety Study of TissueGene-C Mixed With Fibrin-glue for the Patients With Degenerative Arthritis

Kolon Life Science

Status and phase: Completed; Phase 2

Conditions: Degenerative Arthritis

Treatments: Biological: TissueGene-C (High dose); Biological: TissueGene-C (Low dose)

Study type: Interventional

Funder types: Industry

Identifiers

NCT01825811

KS-TGC(S)-01-2

Details and patient eligibility

About

The purpose of this study is to determine whether TissueGene-C, allogeneic human chondrocytes expressing Transforming Growth Factor(TGF)-b1, mixed with fibrin-glue is effective and safe in patients with degenerative arthritis.

Full description

TissueGene-C is a biological new drug which consists of non-transduced chondrocytes and transduced chondrocytes that express TGF-b1 to regenerate the damaged cartilage.

During the clinical trial Phase 2, the investigators compare low dose or high dose TissueGene-C in 12 - months trial with 18 outpatients who have degenerative arthritis. The patients are randomized to two dose levels of TissueGene-C by 1:1 ratio, and they are monitored and recorded for alleviating symptoms, sports activities, function of the knee, and the presence of adverse events.

Enrollment: 18 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Female or male aged 18 years or more
2. Diagnosed with degenerative arthritis of the knee
3. With an IKDC score of 60 or lower at the screening visit
4. With a BMI of higher than18.5 and lower than 30
5. With an International Cartilage Repair Society(ICRS) Grade IV cartilage damage in the major lesions, as confirmed through an MRI scan
6. With major lesions concentrated in one section of the knee, and with the major lesions considered the main cause of the clinical symptoms
7. With major lesions defect size 2 cm2 ~ 10cm2
8. With no alleviation of the symptoms even after at least three months of non-surgical treatment
9. Healthy, with no major findings from the physical examination, hematology, serum chemistry, and urine tests, and no significant medical history
10. Agreed to use an effective contraceptive method during the study period
11. Voluntarily agreed to participate in this study, and signed the informed consent form

Exclusion criteria

1. Showed clinically significant hematology, serum chemistry, and urine test results at the screening visit

2. Mechanical axis (HKA) is greater than 5°

3. Patients receiving injections to the treated knee within 2 months prior to study entry

4. Patients who are pregnant or currently breast-feeding children

5. With another joint disease (e.g., inflammatory arthritis, infectious arthritis)

6. With an infectious disease, including HIV or hepatitis

7. With any of the following clinically significant diseases:

   • heart disease [e.g., myocardial infarction, arrhythmia, other serious heart diseases,

   • kidney disease (e.g., chronic renal failure, glomerulonephritis)

   • liver disease (e.g., liver cirrhosis, fatty liver, acute or chronic liver disease)

   • endocrine disease (e.g., hyperthyroidism, hypothyroidism, thyroiditis, diabetes insipidus, Cushing's disease)

   • insulin-dependent diabetes mellitus

   • medical history of past or current malignant tumor

   • In particular, the tumors that TissueGene-C may aggravate can be screened using the following tests:

     • Leukemia (White Blood Cell level in the hematology)
     • Osteochondroma, Chondromas, Chondroblastoma, Chondromyxoid fibroma, Chondrosarcoma(Alkaline phosphatase level in the hematology)

8. Participated in another clinical trial (using the investigational drug or a medical device) within 30 days before enrollment in this study

9. Considered inappropriate by the investigator for participation in this study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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18 participants in 2 patient groups

TissueGene-C (Low dose)

Experimental group

Description:

TissueGene-C (1.0 x 10\^6 cells per cm\^2 of the cartilage defect) combined with fibrin-glue

Treatment:

Biological: TissueGene-C (Low dose)

Experimental: TissueGene-C (High dose)

Experimental group

Description:

TissueGene-C (3.0 x 10\^6 cells per cm\^2 of the cartilage defect) combined with fibrin-glue

Treatment:

Biological: TissueGene-C (High dose)