Overview

Assessment of Protective Effect of JOINS on Cartilage in Knee Osteoarthritis

Status:
Completed
Trial end date:
2013-09-01
Target enrollment:
0
Participant gender:
All
Summary
- A Pilot study - Randomized and Double-blinded - Placebo controlled - In 2 parallel group (JOINS 200mg:Placebo = 1:1) - Overall 24 months treatment (JOINS:Placebo comparison up to 12 months, Additional follow-up assessment up to 24 months) - Provide rescue medicine throughout whole clinical trial period.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
SK Chemicals Co., Ltd.
SK Chemicals Co.,Ltd.
Criteria
Inclusion Criteria:

1. A female is eligible if she is of:

- Non-child bearing potential (i.e., physiologically incapable of becoming
pregnant), including any female who is at least 2 year after post- menopausal

- Child bearing potential and agrees to the acceptable contraceptive methods used
consistently and correctly

- Pregnancy test result of negative at screening

2. Primary Knee OA(Osteoarthritis) on medial femorotibial compartment based on
ACR(American College Rheumatology) Criteria.

- ACR Criteria : With Knee pain and satisfied at least 1 of 3 (① age > 50 years,
morning stiffness < 30 minute, ③ Presence of Crepitus and Osteophytes on motion)

3. Appropriately signed and dated informed consent has been obtained

Exclusion Criteria:

1. Rheumatoid arthritis or inflammatory arthritis.

2. Bilateral total knee replacement already treated, or planning for the procedure.

3. Knee prosthesis already implanted, or foreseen within the next year.

4. Clinically significant hip osteoarthritis.

5. Severe renal insufficiency defined as creatinine clearance < 30ml/mln(Cockcroft
formula).

6. Clinically significant pulmonary, hepatic, renal or heart disorder or diagnosis
crucial disease by investigator ( Glycosuria(Diabetes mellitus) or asthma patients are
excluded from this clinical study and the patients who has a clinically significant
disease are also excluded.).

7. MRI contraindications : overweight, inferior limb diameter non-fitting the knee
antenna, inserted pace-maker, metallic prosthesis( if known to interfere with MRI
procedure or if known to be unsafe for MRI), metallic clips, insulin pump, cytostatic
pump, hearing aid, essential tremor, claustrophobia, etc,.

8. Allergic reaction to Clinical trial medication.

9. Other clinical trial drugs during the 1 month prior to the screening visit.