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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| TissueGene-C (Low dose) | Experimental | TissueGene-C (1.0 x 10^6 cells per cm^2 of the cartilage defect) combined with fibrin-glue |
|
| Experimental: TissueGene-C (High dose) | Experimental | TissueGene-C (3.0 x 10^6 cells per cm^2 of the cartilage defect) combined with fibrin-glue |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TissueGene-C (Low dose) | Biological | TissueGene-C at 1.0 x 10^6 cells mixed with fibrin-glue |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in IKDC Subjective Knee Evaluation | Symptoms, sports activities, and function of the knee will be measured by the International Knee Documentation Committee (IKDC) | Week 0 and 48 |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in WOMAC scores | Pain, stiffness, and physical function of the knee will be measured by the Western Ontario and McMaster Universities (WOMAC) | Week 0, 24 and 48 |
| Changes in KOOS scores |
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Inclusion Criteria:
Exclusion Criteria:
Showed clinically significant hematology, serum chemistry, and urine test results at the screening visit
Mechanical axis (HKA) is greater than 5°
Patients receiving injections to the treated knee within 2 months prior to study entry
Patients who are pregnant or currently breast-feeding children
With another joint disease (e.g., inflammatory arthritis, infectious arthritis)
With an infectious disease, including HIV or hepatitis
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:
Participated in another clinical trial (using the investigational drug or a medical device) within 30 days before enrollment in this study
Considered inappropriate by the investigator for participation in this study](streamdown:incomplete-link)
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| Name | Affiliation | Role |
|---|---|---|
| Myung Chul Lee, MD, PhD | Seoul National University Hospital | Principal Investigator |
| Chul Won Ha, MD, PhD | Samsung Medical Center | Principal Investigator |
| Seong Il Bin, MD, PhD | Asan Medical Center | Principal Investigator |
| Myung Gu Kim, MD, PhD | Inha University Hospital | Principal Investigator |
| Jae Doo Yoo, MD, PhD | Ewha Womans University Mokdong Hospital | Principal Investigator |
| Hee Su Kyung, MD, PhD | Kyungpook National University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Kyungpook National University Hospital | Daegu | 700-721 | South Korea | |||
| Inha University Hospital |
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| TissueGene-C (High dose) | Biological | TissueGene-C at 3.0 x 10^6 cells mixed with fibrin-glue |
|
Symptoms, pain and functionality of the knee joint will be evaluated via the Knee Injury and Osteoarthritis Outcome Score (KOOS)
| Week 0, 24 and 48 |
| Changes in 100 mm-VAS | Pain of the knee will be measured by the 100mm Visual Analogue Scale (VAS) | Week 0, 24 and 48 |
| Comparative Evaluation of Knee Magnetic Resonance Images (MRIs) | Comparison of pre-procedure MRI scans to those obtained at pre-dosing and at months 6 and 12 by an independent radiographic reviewer | Week 0, 24 and 48 |
| Changes in ICRS Cartilage Repair Assessment | week 0 and 48 |
| Changes in IKDC Subjective Knee Evaluation | Symptoms, sports activities, and function of the knee will be measured by the International Knee Documentation Committee (IKDC) | Week 0 and 24 |
| Changes in KOOS QOL Sub-scale scores | Week 0, 24 and 48 |
| Proportion of Patients Use of Rescue Medication | Week 12, 24 and 48 |
| Incheon |
| 400-711 |
| South Korea |
| Seoul National University Hospital | Seoul | 110-744 | South Korea |
| Samsung Medical Center | Seoul | 135-710 | South Korea |
| Asan Medical Center | Seoul | 138-736 | South Korea |
| Ewha Womans University Mokdong Hospital | Seoul | 158-710 | South Korea |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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