Study of TG-C in Patients With Grade 3 Degenerative Joint Disease of the Knee

Osteoarthritis, Knee Clinical Trial

Official title:

A Phase II Study to Determine the Efficacy and Safety of Allogeneic Human Chondrocytes Expressing TGF-β1 (TissueGene-C) in Patients With Grade 3 Chronic Degenerative Joint Disease of the Knee

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01221441
• Other study ID #: TGC09201
• Status: Completed
• Phase: Phase 2
• First received: October 13, 2010
• Last updated: January 19, 2016
• Start date: May 2011
• Est. completion date: October 2014

Study information

• Verified date: January 2016
• Source: TissueGene, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to see if we can safely regenerate cartilage without invasive surgery using a biologic product called TissueGene-C.

Description:

Protocol TGC09201 is a multi-center, double-blind, placebo-controlled, randomized study. A total of one hundred (100) adults with grade 3 chronic degenerative joint disease (DJD) of the knee joint (as determined by radiographic examination) will be enrolled into the study. TissueGene-C will be administered intra-articularly once via x-ray guidance. TissueGene-C will be administered at a dose of 3 x 10e7 cells. Patients receiving control treatment will receive a single normal saline injection.

The objectives of this study are to:

1. Evaluate the efficacy of TissueGene-C with regard to knee functionality and symptoms of knee osteoarthritis including pain.

2. Evaluate the safety of administration of a single intra-articular dose of TissueGene-C as evidenced by observation of the injection site for irritation or other abnormalities, the incidence and severity of adverse events, and the changes in physical examination findings and laboratory tests, including immune analyses.

3. Evaluate the incidence and dose of analgesia and/or anti-inflammatory medication.

4. Evaluate the regeneration of hyaline cartilage as determined by 3T magnetic resonance imaging (MRI).

5. Evaluate distribution of hChonJb#7 cells out of the injection site.

6. Evaluate the efficacy of TissueGene-C by evaluating the need for total knee arthroplasty after treatment

Recruitment information / eligibility

• Status: Completed
• Enrollment: 102
• Est. completion date: October 2014
• Est. primary completion date: October 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Male or Female subject

2. Age 18 to 70 years

3. In general good health as evidenced by physical examination, normal hematology, serum chemistry, and urinalysis screening laboratory results, and a negative history of significant organ system disorders. All laboratory values must be within 20% of normal ranges.

1. Body Mass Index (BMI) should be between '18.5 - 45.5'. The applied scale is the same for both men and women.

2. Blood Pressure measurements - Systolic Blood Pressure should be between 90-160mm. Hg, and Diastolic Blood Pressure between 50-90mm.Hg,

4. Patients with Grade 3 chronic osteoarthritis of the knee as determined by the Radiographic Criteria of Kellgren and Lawrence.

5. Symptom of pain for more than four (4) consecutive months and intensity of = 40 and = 90 on the 100-mm scale.

6. Patients should be cleared to use protocol specified equipment: 3T MRI.

7. Patients providing written informed consent after the nature of the study is fully explained and understood by the patient.

Exclusion Criteria:

1. Age 71 or older

2. Patients with abnormal hematology, serum chemistry, or urinalysis screening laboratory results.

3. Patients taking non-steroidal anti-inflammatory medications within 14 days of baseline visit unless washed out as per section 3.6.4 above.

4. Patients taking steroidal anti-inflammatory medications within 2 months of baseline visit.

5. Patients with a recent (within 1 year) history of drug abuse and/or a positive urine drug test at the time of screening.

6. Patients receiving injections to the treated knee within 2 months prior to study entry

7. Patients who are contraindicated for 3T MRI.

8. Patients who are pregnant or currently breast-feeding children.

9. Patients with systemic, rheumatic or inflammatory disease of the knee or chondrocalcinosis, hemochromatosis, inflammatory arthritis, necrosis of the femoral condyle, arthropathy of the knee associated with juxta-articular Paget's disease of the femur or tibia, ochronosis, hemophilic arthropathy, infectious arthritis, Charcot's knee joint, villonodular synovitis, synovial chondromatosis, and/or history of inflammatory arthropathy.

10. Patients with ongoing infectious disease, including HIV and hepatitis B or C.

11. Patients with clinically significant cardiovascular, renal, hepatic, endocrine disease, cancer, or Type I diabetes.

12. Patients participating in a study of an experimental drug or medical device within 30 days of study entry.

13. Patients that will be unable to comply with the requisite study follow-up and are not able to complete all of the follow-up office visits and 3T MRI exams.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Joint Diseases
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Biological:
• TissueGene-C
Single intraarticular injection at 3 x 10e7 cells

Drug:
• Normal Saline
Single intraarticular injection of normal saline as a placebo control

Locations

Country	Name	City	State
United States	Commonwealth Orthopedics	Arlington	Virginia
United States	Sinai Hospital of Baltimore	Baltimore	Maryland
United States	Rothman Institute	Philadelphia	Pennsylvania
United States	Advent Clinical Research	Pinellas Park	Florida
United States	University Orthopedics	State College	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
TissueGene, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline in the International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Score at 1 Year	Symptoms, pain and function of the knee joint determined and scored using the International Knee Documentation Committee (IKDC) Subjective Knee Evaluation (Total Score, range 0-100 with higher scores better). Linear mixed model used for analysis.	1 Year	No
Primary	Change From Baseline in Visual Analog Scale (VAS) Score at 1 Year	Reduction in pain as measured by a 100 mm visual analog scale (0= no pain; 100 = extreme pain) from Baseline to 1 Year. Linear mixed model used for analysis.	1 Year	No
Secondary	Change From Baseline in Knee Injury and Osteoarthritis Outcome Score (KOOS) at 2 Years	Symptoms, pain and functionality of the knee joint as determined by Total Score of the Knee Injury and Osteoarthritis Outcome Score (KOOS) (Range 0-100 with higher scores indicating healthier outcomes). Linear mixed model used for analysis.	2 Years	No
Secondary	Change From Baseline in Articular Cartilage Damage in the Knee as Determined by the Lysholm Knee Score at 2 Years	Measurement to assess outcomes of various chondral disorders of the knee determined by the Lysholm Knee Scale (Range 0-100 with higher scores better). Linear mixed model used for analysis.	2 Years	No
Secondary	Comparative Evaluation of Knee Magnetic Resonance Images (MRIs) From Baseline to 1 Year	Comparison of pre-procedure 3T MRI scans to those obtained at months 12 following dose administration by an independent radiographic reviewer. Evaluations will be scored using Whole Organ Magnetic Resonance imaging Score (WORMS) Cartilage Morphology Subscore (Range 0-6, with higher scores being worse)	1 Year	No
Secondary	Change in Pain Severity From Baseline to 2 Years as Assessed by Questionnaire	Change in pain severity (on a scale from 1 to 4) from baseline to 2 years as measured by a questionnaire (lower scores better)	2 Years	No
Secondary	Number of Participants With Change in Pain Severity Measured by Incidence and Dose of Analgesia	The number of participants that had a change in pain severity as measured by the incidence and dose of analgesic medications	2 Years	No
Secondary	Change From Baseline in Knee Function as Determined by the Lower Extremity Functional Scale at 2 Years	Assessment of knee function as determined by the Lower Extremity Functional Scale (LEFS); change from baseline to 2 years (Range 0-80 with higher scores signifying lower difficulty in performing knee functions)	2 Years	No
Secondary	The Incidence of Total Knee Arthroplasty	Quantification of the incidence of total knee arthroplasty of the treated knee subsequent to treatment with TissueGene-C	2 Years	No
Secondary	The Number of Patients Experiencing Injection Site Reactions Related to Treatment	The number of patients with observations of the administration site deemed related to treatment with either active or placebo, including arthralgia, swelling, irritation, pain, stiffness or abnormalities	2 Years	Yes
Secondary	The Incidence and Severity of Adverse Events in Treated Patients	The incidence and severity of adverse events assessed through 104 weeks (2 years) after dose administration	2 Years	Yes
Secondary	Number of Participants With Adverse Events Due to Clinically Significant Changes in Hematology and Urinalysis Tests	The number of participants with changes in clinical hematology, chemistry, and urinalysis test results through 2 years that were considered Adverse Events	2 Years	Yes
Secondary	Change in SF-36 General Health Assessment Questionnaire (Overall Score) From Baseline to 2 Years	Overall assessment of general health as determined by scoring use an SF-36 Questionnaire (Range 0-100 with higher scores better - indicating less disability)	2 Years	No