The Efficacy and Safety of Invossa K Injection in Patients Diagnosed With Knee Osteoarthritis

Kolon Life Science

Status and phase: Unknown; Phase 3

Conditions: Osteoarthritis

Treatments: Biological: Invossa K Inj.; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT03383471

KS-INV-02-3

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and safety of intraarticular Invossa K Injection patients diagnosed with Kellgren & Lawrence grade 2 knee osteoarthritis.

Enrollment: 146 estimated patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female aged 19 and older

2. Patients with IKDC Subjective Knee Evaluation of ≤ 60 of the target knee.

3. Patients with a score of ≥ 40 on the 100 mm pain VAS of the target knee.

4. Patients with grade 2 osteoarthritis as determined by the radiographic criteria of Kellgren and Lawrence

5. BMI should fall between 18.5 and 30

6. Patients who satisfies the clinical/radiational criteria by the American College of Rheumatology guidelines, and applies to one of the following.

   • Age > 50 years old
   • Morning stiffness < 30 minutes
   • Crepitus and Osteophytes

7. With major lesions concentrated in one section of the knee, and with the major lesions considered the main cause of the clinical symptoms

8. Patients with persistent symptoms in spite of conservative therapy for more than 3 months : Improvement of 100 mm VAS are less than 10 mm after 3 months

9. Healthy, with no major findings from the physical examination, hematology, serum chemistry, and urine tests, and no significant medical history

10. Agreed to use an effective contraceptive method during the study period

11. Voluntarily agreed to participate in this study, and signed the informed consent form

Exclusion criteria

1. Patients who had been administered with drugs such as oriental medicine, glucosamine and chondroitin within 14 days of baseline visit (But, possible to include after 14 days of wash-out period)

2. Patients taking steroidal anti-inflammatory medications within 14 days of baseline visit (But, possible to include after 14 days of wash-out period)

3. Patients with severe pain in other areas that could effect the diagnosis of the symptoms

4. Patients over Grade 3 osteoarthritis as determined by the radiographic criteria of Kellgren and Lawrence

5. History of surgery like arthroendoscopy within the past 6 months on the target knee

6. Patients who had been administered with immunosuppressants, including antirheumatic drugs (including methotrexate or antimetabolite), within the past 3 months

7. History of injection within the past 3 months on the target knee

8. Pregnant or breastfeeding female

9. With another joint disease apart from degenerative arthritis

10. Patients with hepatitis including carrier

11. Patients with HIV and an infectious disease which is clinically uncontrolled

12. Patients who have any of the following clinically significant diseases or have a medical history within 6 months :

    • Clinically significant heart diseases which are considered by the investigator
    • Uncontrolled hypertension : if the systolic blood pressure exceeds 160 mmHg or diastolic blood pressure exceeds 100 mmHg in a sitting position
    • Kidney disease
    • Liver disease
    • Endocrine disease
    • Uncontrolled diabetes mellitus : HbA1c ≥ 9%
    • Paget's disease, ochronosis, acromegaly, hemochromatosis, Wilson's disease
    • Genetic diseases (hyperkinesia, collagen gene abnormality)

13. Medical history of past or current malignant tumor

14. Patients with a history of anaphylactic reactions

15. Patients with a history of hypersensitivity reactions to the components of this drug, including dimethylsulfoxide, mannitol, dextran 40 or bovine proteins

16. Participated in another clinical trial (using the investigational drug or a medical device) within 30 days before enrollment in this study

17. Patients who administered the INVOSSA K inj.

18. Considered inappropriate by the investigator for participation in this study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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146 participants in 2 patient groups, including a placebo group

Invossa K Inj.

Experimental group

Description:

Invossa K Inj.

Treatment:

Biological: Invossa K Inj.

Placebo

Placebo Comparator group

Description:

Placebo control

Treatment:

Drug: Placebo