A Multi-center, Randomized, Double-Blinded, Active-Controlled, Phase II Clinical Trial to Evaluate Efficacy and Safety of SMUP-IA-01 in Patients With Knee Osteoarthritis
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 94
- 试验地点
- 5
- 主要终点
- Change in the WOMAC(Western Ontario and McMaster University Osteoarthritis Index) total score at post-dose 52 weeks from baseline
研究概览
简要总结
This clinical trial is for patients who have been diagnosed with Kellgren-Lawrence (K&L) Grade 2 or 3 knee osteoarthritis on radiographic examination. Only subjects who voluntarily agree to participate by filling out the written Informed Consent document will undergo screening for subject selection (inclusion/exclusion) criteria, at which time the severity of OA in each knee will be used to determined which knee will be treated (index knee - i.e., the more severely affected knee), and enroll in this study.
详细描述
Patients who meet the inclusion/exclusion criteria will be randomly assigned at visit 2 to either of study group 1(low-dose), study group 2 (mid-dose) or active control group at 1:1:1 ratio. Patients will be administered with investigational product. Investigational product will be administered into the to-be-treated (index) knee one time within 7 days after randomization.
All patients enrolled will be followed up a total of 6 times (1, 4, 8, 12, 24, and 52 weeks) for up to post-dose 12 months. The patients should visit the study facility according to the visit schedule, and will undergo safety evaluation (vital sign, laboratory test, etc.) and efficacy evaluation [Western Ontario and McMaster Universities osteoarthritis index (WOMAC), 100-mm visual analogue scale (VAS), International Knee Documentation Committee (IKDC) subjective knee evaluation].
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who are ≥ 19 years of age on the date on which the consent form was signed
- •Patients diagnosed with knee osteoarthritis in at least one knee according to the clinical and radiological definition criteria of American College of Rheumatology (ACR) guidline at screening visit
- •Patients with knee OA corresponding to K&L Grade 2 or 3 on radiographic examination at screening visit
- •Patients with less than 35 of BMI at screening visit
- •Patients who voluntarily decide to participate and sign the consent form
- •Patients who have persistent symptoms despite having undergone a reasonable trial of standard therapy (i.e., for a minimum of 3 months)
排除标准
- •Patients with any of the following diseases.
- •infectious arthritis, autoimmune or inflammatory joint diseases, gout, recurrent pseudogout, Paget's disease, intra-articular displaced fracture, ochronosis, acromegaly, haemochromatosis, Wilson's disease, genetic disease (hyperkinesia etc.), genetic collagen disorder, etc.
- •Patients who have ever undergone surgery or radiotherapy in the knee joint area within the 12 weeks prior to the screening visit date, or who have not been recovered from its side effect yet.
- •Patients with SIF (Subchondral insufficiency fracture) corresponding to type II of the RPOA (rapidly progressive osteoarthritis).
- •Patients whose physical examination results show severe degree of ligament instability.
- •Patients who have ever been given any intraarticular drug injection (i.e., hyaluronic acid injection, etc.) in to-be-treated (index) knee within the 6 months, prior to the screening visit date.
- •Patients who have ever been given steroids via intraarticular injection in to-be-treated (index) knee within the 12 weeks prior to the screening visit date.
- •Patients who have ever taken medications or given therapy below within the past 2 weeks on the basis of screening visit date. However, if patients have 14 days of wash-out period, the patient is allowed to participate.
- •drugs containing the ingredient of glucosamine, chondroitin sulfate, or diacerein
- •drugs containing herbal ingredient or herbal drugs for knee OA pain relief
- •anti-inflammatory analgesics or NSAIDs (prescription/non-prescription drugs). (However, patients who take acetaminophen and have 3 days of wash-out period are allowed to participate.)
- •oral steroids
- •hospital physiotherpy or oriental medicine treatment (buhang, acupunture, moxibustion etc.)
- •Patients who have skin disease on injection site or who are judged inappropriate for intra-articular injection on to-be-treated knee.
- •Patients who are judged unsuitable for MRI scanning (3.0 Tesla or higher) due to an insertion of metal material (i.e., heart pacemaker, cerebral aneurysm clip, etc.) or obstructive phobia. However, patients who have an insertion of metal material that is not affected by the magnetic field is allowed to participate
- •Patients with clinically significant past or present illness as follows;
- •heart diseases (i.e., myocardial infarction, coronary artery bypass surgery, arrhythmia and other serious heart diseases, etc.)
- •uncontrolled hypertension (not controlled down to 140/90 mmHg or below even after treatment with 3 or more antihypertensive drugs)
- •kidney disease (i.e., chronic kidney failure, glomerulonephritis, etc.)
- •liver disease (i.e., acute or chronic liver disease such as cirrhosis, fatty liver, etc.)
- •endocrine diseases (i.e., thyroiditis, diabetes insipidus, Cushing's disease, etc.)
- •other serious systemic diseases
- •Patient with ongoing autoimmune disorder that requires treatment with an immunosuppressive medication
- •Patients with infection that requires administration of parenteral antibiotics
- •Patients with a history of mental illness or epilepsy
- •Patients who have been diagnosed with cancer within the 5 years prior to the screening visit date
- •Patients who have been given immunosuppressive drugs such as cyclosporin A or azathioprine within the 6 weeks prior to the screening visit
- •Patients with a history of allergic reactions to hyaluronic acid injections, cryoprotectant (dimethyl sulfoxide, DMSO), or gentamicin.
- •Patients who are pregnant or lactating, or patients who have a plan to become pregnant during the study period
- •Male or female patients who do not agree to avoid pregnancy or the use of appropriate contraceptive methods during the study period. But women who have given infertility surgery or who have passed menopause one year or more are allowed to participate without the consent for contraception.
- •Patients who have been given any other cell therapy products or who plan to do so during the study period.
- •Patients who have been given any other investigational products including device within the 3 months prior to the screening visit date.
- •Patients who are judged by the investigator as inappropriate for enrollment into the study, for any reasons other than the reasons specified above.
研究组 & 干预措施
Study Group 1: SMUP-IA-01 (low dose)
Investigational Product - 4.0×10^6 cells/2 mL of SMUP-IA-01 (2 ml of 1% sodium hyaluronate injection is administered before administration of SMUP-IA-01)
干预措施: SMUP-IA-01(low dose) (Biological)
Study Group 2:SMUP-IA-01 (mid dose)
Investigational Product - 1.0×10^7 cells/2 mL of SMUP-IA-01 (2 ml of 1% sodium hyaluronate injection is administered before administration of SMUP-IA-01)
干预措施: SMUP-IA-01(mid dose) (Biological)
Active Control Group
Investigational Product - 2 ml of 1% sodium hyaluronate (2 ml of sodium chloride injection is administered before administration of 1% sodium hyaluronate)
干预措施: Active Control Group Sodium chloride (Drug)
结局指标
主要结局
Change in the WOMAC(Western Ontario and McMaster University Osteoarthritis Index) total score at post-dose 52 weeks from baseline
时间窗: Baseline, 52 week
Total score is between 0 point (no symptoms) \~ 96 points (higher score representing worse symptoms).
次要结局
- Change in the WOMAS(whole-organ magnetic resonance imaging score) at post-dose 52 weeks from the baseline(Baseline, 52 week)
- Change in K&L grade, joint space width, mechanical axis, and anatomical axis at post-dose 52 weeks from the baseline(Baseline, 52 week)
- Chage amount of WOMAC score by item (pain, stiffness, physical function) at post-dose 24 weeks and 52 weeks from the baseline(Baseline, 24 week, 52 week)
- Chage amount of 100-mm VAS((Visual Analogue Scale) at post-dose 1 week, 4 weeks, 8 weeks, 12 weeks, 24 weeks and 52 weeks from the baseline(Baseline, 1 week, 4 week, 8 week, 12 week, 24 week, 52 week)
- Percentage of patients who took the rescue drugs and dosage at post-dose 1 week, 4 weeks, 8 weeks, 12 weeks, 24 weeks and 52 weeks(1 week, 4 week, 8 week, 12 week, 24 week, 52week)
- Chage amount of IKDC(International Knee Documentation Committee) at post-dose 1 week, 4 weeks, 8 weeks, 12 weeks, 24 weeks and 52 weeks from the baseline(Baseline, 1 week, 4 week, 8 week, 12 week, 24 week, 52 week)
- Change amount of biomarkers at post-dose 1 week, 4 weeks, 8 weeks, 12 weeks, 24 weeks and 52 weeks against the baseline; serum CTX-I, Serum HA, Serum MMP-3, Urine CTX-I, Urine CTX-II.(baseline, 1 week, 4 week, 8 week, 12 week, 24 week, 52week)
- Change amount of WOMAC total score at post-dose 24 weeks from the baseline(Baseline, 24 week)
- Change in T2 mapping at post-dose 52 weeks from the baseline(Baseline, 52 week)