Clinical Trial of Allogenic Adipose Tissue-Derived Mesenchymal Progenitor Cells Therapy for Knee Osteoarthritis

A Phase I, Randomized, Single-centered, Double-blinded Clinical Trial of Allogenic Adipose Tissue-Derived Mesenchymal Progenitor Cells Therapy for Knee Osteoarthritis

Evaluate the safety and efficacy of Allogenic Adipose Tissue-Derived Mesenchymal Progenitor Cells Therapy for Knee Osteoarthritis.

Study Overview

• Status: Completed
• Conditions: Osteoarthritis
• Intervention / Treatment: Biological: Mesenchymal progenitor cells

Detailed Description

A Phase I, Randomized, Single-centered, Double-blinded Clinical Trial of Allogenic Adipose Tissue-Derived Mesenchymal Progenitor Cells Therapy for Knee Osteoarthritis.

This is a randomized,single-blind, double-blinded,phase I clinical trial. Subjects who are with a clinical diagnosis of knee osteoarthritis cartilage defects and will be randomly distributed 1:1:1 to different dosage group after signing the ICF and screening tests.The treatment will accept Allogenic ReJoinTM at the first and fourth week.The duration of the therapy is 48 weeks.

• Study Type: Interventional
• Enrollment (Actual): 22
• Phase: Phase 1

Contacts and Locations

Study Locations

• China
  • Shanghai
    • Shanghai, Shanghai, China, 200127
      • Department of Rheumatology,Ren Ji Hospital,School of Medicine,Shanghai Jiao Tong University,Shanghai,China

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Object has an allergic history or is of an allergic constitution.
• Subjects who understand and sign the consent form for this study.
• Age: 18-70, males and females.
• Clinical diagnosis of degenerative arthritis by Radiographic Criteria of KellgrenLawrence:Duration of pain over Grade 4(11-point numeric scale)> 4 months.
• Course of Knee osteoarthritis:6 months to 10 years;
• The VAS score :3-8 points.(the data acquisition time is to stop using all analgesic at least 3 days ).

Exclusion Criteria:

• The subject has an allergic history of medicine or food。.
• The subject'BMI is over 30.
• The subject has uncontrolled or hard-to-control diseases of cardiovascular, liver, kidney or lung， endocrine system.
• The subject has an history malignant tumour.
• The subject has complications or diseases of: systemic or rheumatoid arthritis, Chondrocalcinosis articularis， Hemochromatosis，inflammatory arthropathy，avascular necrosis of femoral head，Paget's disease，hemophilic arthropathy，infectional arthritis，Charcot's disease，villonodular synovitis or synovial chondromatosis.
• The subject has severe generalized infectious diseases or local knee infection in the 3 months prior to this trial.
• The subject has disease of lower limbs which may be interfered knee evaluation, for example fibromyalgia, osphyalgia, lumbar disc protrusion and so on.
• The subject has coagulation disorders.
• The subject has received arthroscopic surgery or intra-articular operations in the 6 months prior to this trial.
• The subject has received other intra-articular injections for KOA in the 6 months preceding the trial.
• The subject has received aminoglucose or chondroitin sulfate in the 6 months preceding the trial.
• The subject has plan of knee prosthesis within the trial.

• The subject has contraindication of MRI, included but not only: the subject installed heart pacemaker、defibrillator、heart bracket、heart valve prosthesis、metal clip after aneurysm surgery、drug infusion device implanted in vivo、any electronic device implanted in the body（nerve stimulator、bone growth stimulator）、endovascular coil、strainer、ECG monitor、metal suture、shrapnel or sand of body, plate fixation and steel nail after fracture

  - Page 4 of 4 [DRAFT] - surgery、artificial limb or joint、audiphone、artificial cochlea、middle ear shift plant、metallic intraocular foreign body etc； claustrophobia、pregnancy within 3 months、critically ill patients.

• The subject tests positive for: HIV, hepatitis virus, syphilis or other infectious diseases.
• The subject has history of alcoholism, drug abuse, or mental illness in the 3 years prior to this trial.
• The subject has participated in any other clinical trial in the 3 months prior to this trial.
• The subject is pregnant, lactating or planning to conceive within the next 6 months.
• The subject has any other unsuitable or adverse condition to be determined by the investigator.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Mesenchymal progenitor cells Dosage 1; Mesenchymal progenitor cells low-dose group	Biological: Mesenchymal progenitor cells; Biological: Allogenic Adipose tissue-derived mesenchymal progentior cells administrated for intra-articular use
Other: Mesenchymal progenitor cells Dosage 2; Mesenchymal progenitor cells mid-dose group	Biological: Mesenchymal progenitor cells; Biological: Allogenic Adipose tissue-derived mesenchymal progentior cells administrated for intra-articular use
Other: Mesenchymal progenitor cells Dosage 3; Mesenchymal progenitor cells high-dose group	Biological: Mesenchymal progenitor cells; Biological: Allogenic Adipose tissue-derived mesenchymal progentior cells administrated for intra-articular use

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Safety, recording of Adverse Events and Serious Adverse Events	12 weeks,48 weeks
WOMAC Score	48 weeks

Secondary Outcome Measures

Outcome Measure	Time Frame
VAS Score	48 weeks
SF-36	48 Weeks
The volume of articular cartilage	48 weeks
WORMS Score	48 weeks

Collaborators and Investigators

• Sponsor: Cellular Biomedicine Group Ltd.
• Collaborators: RenJi Hospital

Publications and helpful links

General Publications

• Zhao X, Ruan J, Tang H, Li J, Shi Y, Li M, Li S, Xu C, Lu Q, Dai C. Multi-compositional MRI evaluation of repair cartilage in knee osteoarthritis with treatment of allogeneic human adipose-derived mesenchymal progenitor cells. Stem Cell Res Ther. 2019 Oct 21;10(1):308. doi: 10.1186/s13287-019-1406-7.

Study record dates

Study Major Dates

• Study Start (Actual): December 1, 2015
• Primary Completion (Actual): March 1, 2018
• Study Completion (Actual): March 1, 2018

Study Registration Dates

• First Submitted: December 21, 2015
• First Submitted That Met QC Criteria: December 24, 2015
• First Posted (Estimate): December 30, 2015

Study Record Updates

• Last Update Posted (Actual): September 13, 2018
• Last Update Submitted That Met QC Criteria: September 12, 2018
• Last Verified: September 1, 2018

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Arthritis; Osteoarthritis; Osteoarthritis, Knee
• Other Study ID Numbers: CBMG-Allo-KOA-1.1