Evaluating CartiLife® for knee cartilage defects

A Multi-Center, Open-Label, Phase 2 Trial to Evaluate the Efficacy and Safety of CartiLife® for Patients With Articular Cartilage Defects in the Knee

This study is testing if a new treatment using patients' own cartilage cells can help adults with knee cartilage damage feel better and improve their knee function.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 25 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Biosolution Co., Ltd. (Industry-sponsored)
• Drugs / interventions: chemotherapy, radiation
• Locations: 5 sites (Irvine, California and 4 other locations)
• Trial ID: NCT04744402 on ClinicalTrials.gov

What this trial studies

This phase 2 clinical trial aims to assess the safety and efficacy of CartiLife®, a pellet-type extracellular matrix-associated autologous chondrocyte treatment, for adults suffering from articular cartilage defects in the knee due to trauma or degeneration. Participants will receive an implantation of their own cultivated chondrocytes, and the study will measure outcomes related to structural regeneration, function, and pain relief at 48 weeks post-treatment. The trial is open-label, meaning both the researchers and participants will know the treatment being administered.

Who should consider this trial

Good fit: Ideal candidates are adults over 18 with specific cartilage lesions in the knee that meet defined size and severity criteria.

Not a fit: Patients with less severe cartilage defects or those with unstable knee conditions may not benefit from this treatment.

Why it matters

Potential benefit: If successful, this treatment could significantly improve knee function and reduce pain for patients with cartilage defects.

How similar studies have performed: Previous studies on autologous chondrocyte implantation have shown promising results, suggesting potential success for this approach.

Eligibility criteria

Inclusion Criteria:

In order to be eligible to participate in this study, an individual must meet all of the following:

1. Male or female subjects aged over 18 at the time of signing the Informed Consent form
2. Subject who has a size of the relevant cartilage lesion ≥ 2 cm2 and ≤ 10 cm2 but with a defect area total volume ≤ 4 cm3
3. Subject with isolated International Cartilage Repair Society (ICRS) Grade III or IV chondral lesion on articular cartilage
4. Subject who has a lower extremity alignment within 5 degrees of the neutral weight bearing axis
5. Subject who can move independently and has a mechanically stable knee (normal ligament status)
6. Subject with intact or partial meniscus status (\>50% of meniscus)
7. Subject who has KOOS pain value less than 60 at baseline
8. Subject who agrees to actively participate in a rehabilitation protocol and follow-up program
9. Subject who is able to provide informed consent and comply with study requirements
10. Subject who is willing to discontinue any nonsteroidal anti-inflammatory drugs (NSAIDs) except rescue medication (\< acetaminophen 4 g per day) 7 days prior to visit
11. Subject who has Body Mass Index (BMI) ≤ 37 kg/m2
12. Female and male subjects of childbearing potential who are willing to use adequate contraception methods for the duration of the trial.

Exclusion Criteria:

Individuals who meet any of the following will be excluded from participation in this study:

1. Subject who has inflammatory articular diseases such as rheumatoid arthritis or gout or pseudogout
2. Subject who has radiographic evidence of grade 4 osteoarthritis based on the Kellgren and Lawrence criteria
3. Subject who has received an intra-articular treatment within the last 3 months
4. Subject who has had a surgical procedure on the knees within the last 6 weeks (Subjects can be considered enrollment per the investigator's discretion)
5. Subject who has a condition in another lower extremity joint that interferes with the function of the index knee
6. Subject who would receive a concomitant surgical procedure on the knees at the time of the study treatment
7. Subject whose articular cartilage defect is asymptomatic
8. Subject who has any clinically significant disease, which is judged by the investigator to affect this clinical trial, including but not limited to diabetes not adequately controlled, bleeding diathesis or hematologic disease, endocrinopathies, cardiovascular disease, renal disease (severe renal impairment), autoimmune disease, inflammatory arthritis, and current infectious disease
9. Subject with other diseases including tumors except for cartilaginous defects of joints
10. Subject who has a history of hypersensitivity to gentamicin, other aminoglycosides, or products of porcine or bovine origin
11. Subject who participates in concurrent trials or in previous trial within 30 days of signing informed consent
12. Subject who has any radiation therapy or chemotherapy within 2 years prior to screening
13. Subject who is currently pregnant or nursing
14. Subject who has any degenerative muscular, connective tissue or neurological condition or other disease process that would interfere with healing or the evaluation of outcome measures.
15. Subject with known HIV infection, active hepatitis C and/or hepatitis B infection
16. Subject who has ligament instability \> Grade 1
17. Subject who is an active drug/alcohol abuser or has a history of alcohol or drug abuse during the last two years.
18. Subject who has significant lab abnormalities for the following parameters (If the value is within 10% of the listed laboratory exclusion criterion value and the value is considered not to be clinically significant by the investigator, the subject can be considered for enrollment):

    * Serum ALT and AST \> 3 x upper limit of normal
    * Serum creatinine \> 1.5 x upper limit of normal
    * PT/INR out of normal range
    * Hemoglobin \< 10 g/dL for female subject and hemoglobin \< 11 g/dL for male subject
    * Platelets out of normal range
    * Hemoglobin A1c levels \> 9%

Where this trial is running

Irvine, California and 4 other locations

• Tilda Research — Irvine, California, United States (Not_yet_recruiting)
• Biosolutions Clinical Research Center — La Mesa, California, United States (Recruiting)
• Horizon Clinical Research — La Mesa, California, United States (Recruiting)
• Lafayette General Health — Lafayette, Louisiana, United States (Recruiting)
• Ohio State University — Columbus, Ohio, United States (Recruiting)

Study contacts

• Study coordinator: TaeKyung Kim, MA

Conditions Articular Cartilage Defect; Articular Cartilage Degeneration