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Clinical Trials/JPRN-jRCT2080223482
JPRN-jRCT2080223482
Completed
Phase 3

A Phase III Study of SI-613 in Patients with Knee Osteoarthritis (confirmatory study)

SEIKAGAKU CORPORATIO0 sites440 target enrollmentStarted: March 14, 2017Last updated:

Overview

Phase
Phase 3
Status
Completed
Sponsor
SEIKAGAKU CORPORATIO
Enrollment
440

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
>= 40age old to <= 75age old (—)
Sex
All

Inclusion Criteria

  • Diagnosis of osteoarthritis of the knee according to American College of Rheumatology criteria at the time of screening.
  • Kellgren\-Lawrence score grade 2 or 3 in an Antero\-posterior weight\-bearing x\-ray of the target knee joint in the standing position taken at the time of screening.
  • Subjects who are willing to discontinue pain medication except as permitted per protocol from the start date of screening to the end of Week 24 after the first injection (using acetaminophen as a rescue medication is permitted for breakthrough pain control).

Exclusion Criteria

  • Secondary OA resulting from trauma or the other diseases in the target knee
  • Subjects who have pain in lower extremity other than knee OA if it would interfere with the evaluation of the target knee or have OA of the hip or ankle at screening and Week 0 before injection.

Investigators

Sponsor
SEIKAGAKU CORPORATIO

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