IA Injection of Rejoint Gel and PRP in Patients With Unilateral Knee OA

NCT ID: NCT04519047

Last Updated: 2020-08-24

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-08-13
• Study Completion Date: 2021-12-31

Brief Summary

To assess the safety and tolerability of intra-articular Injection doses of Rejoint Gel after platelet-rich plasma administration in unilateral knee OA subjects.

Detailed Description

This single-center, randomized, double-blind, feasibility study to evaluate the safety and potential for effectiveness of an intraarticular Injection of Rejoint Gel after platelet-rich plasma administration in patient with single knee OA, parallel-design study will enroll approximately eligible 30 subjects with single knee OA.

The subjects will be randomized (1:1) to receive 1 of 2 treatments below:

1. Treatment Group: Rejoint Gel, intra-articular injection, with platelet-rich plasma (PRP) in 2:1 volume ratio or

2. Control Group: Normal saline, intra-articular injection with PRP in 2:1 volume ratio Beginning on treatment period, subjects will receive a single treatment cycle of either 150 mg/ml Rejoint Gel or normal saline with PRP intra-articular injection twice for one month (Visit 3 and 4). Subjects will be followed to Visit 5, 6 and 7 for safety and potential for effectiveness assessments.

Conditions

PRP; Knee Osteoarthritis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Rejoint

Rejoint+PRP

Group Type: EXPERIMENTAL

PRP

Intervention Type: BIOLOGICAL

Beginning on treatment period, subjects will receive either Rejoint Gel or normal saline with PRP intra-articular injection twice for one month (Visit 3 and 4).

Control

Saline+PRP

Group Type: ACTIVE_COMPARATOR

PRP

Intervention Type: BIOLOGICAL

Beginning on treatment period, subjects will receive either Rejoint Gel or normal saline with PRP intra-articular injection twice for one month (Visit 3 and 4).

Interventions

PRP

Beginning on treatment period, subjects will receive either Rejoint Gel or normal saline with PRP intra-articular injection twice for one month (Visit 3 and 4).

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Written informed consent before any study-specific procedure is performed;

2. Ages of 45~80 years old on the day of consent;

3. The patient is able to understand the nature of the study;

4. Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2;

5. Patient was diagnosed as OA of single knee joint by American College of Rheumatology (ACR) criteria; [i.e, knee pain, and any one of the following: age> 45 years, crepitus, or morning stiffness<30 minutes in duration, or confirmed through radiographic X ray];

6. Knee WOMAC Pain Score (sum of five components) between 20 and 40 score, after 15 meters of walking pain;

7. Contralateral knee WOMAC Pain Score <15 score;

8. Never receiving intra-articular hyaluronic acid (HA) injections of the knee, or last received intra-articular HA more than 6 months;

9. Patient meets below conditions by blood test, kidney and liver function test :

White blood cell (WBC) count > 3,000/μL Absolute neutrophil count (ANC) ≥ 1,500/μL Hemoglobin (Hb) ≥ 9.0 g/dL Thrombocyte count > 50,000/μL Blood urea nitrogen (BUN) and serum Creatinine ≤ 3X Upper Limit of Normal (ULN) Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 3 x ULN

Exclusion Criteria

1. Known sensitivity to mPEG-PLGA hydrogel (Rejoint Gel);

2. Infection in the joint or surrounding skin;

3. Known Intra-articular neoplasm;

4. Inflammatory joint disease, OA in the hips, osteonecrosis, moderate to marked effusion from index knee;

5. Documented current positive synovial fluid culture;

6. Large knee circumference (>45 cm);

7. History of herpes zoster in the past 3 months;

8. Last receiving the treatment of immunosuppressants, anti-coagulants, Non-steroidal anti-inflammatory Drugs (NSAIDs), antidepressants 14 days prior to study randomization;

9. Planned knee surgery in the next 6 months or received knee surgery in the past 6 months;

10. Subject is receiving or is less than 28 days since ending other investigational device or drug;

11. Known full-thickness cartilage loss in index knee;

12. Documented fibromyalgia, or hemiparesis;

13. Evidence of signs or symptoms of a viral, bacterial, or fungal infection occur 14 days prior to the study treatment starts, per the assessment of the investigator;

14. Any major medical or psychiatric disorder that in the opinion of the investigator, might prevent the subject from completing the study or interfere with the interpretation of the study results, such as terminal diseases, malignant tumors, heart failure (NYHA II-IV), coronary arterial disease, uncontrolled hypertension, uncontrolled diabetes, peripheral arterial disease or dementia, might prevent the subject from completing the study or interfere with the interpretation of the study results;

15. Pre-menopausal females of childbearing potential not willing to use acceptable method(s) of birth control during treatment;

16. Female subject who is lactating or pregnant

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The Industrial Technology Research Institute

OTHER

Sponsor Role: collaborator

National Taiwan University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Chueh-Hung Wu, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

National Taiwan University Hospital

Taipei, , Taiwan

Site Status: RECRUITING

Countries

Taiwan

Central Contacts

Chueh-Hung Wu, MD, PhD

Role: CONTACT

nojred@gmail.com

+886223123456 ext. 66473

Facility Contacts

Chueh-Hung Wu, MD, PhD

Role: primary

nojred@gmail.com

886223123456 ext. 66473

Other Identifiers

201812157DSA

Identifier Type: -

Identifier Source: org_study_id