Status:

COMPLETED

Study Evaluating AGG-523 in Subjects With Severe Osteoarthritis Requiring Total Knee Replacement

Lead Sponsor:

Wyeth is now a wholly owned subsidiary of Pfizer

Conditions:

Osteoarthritis

Eligibility:

All Genders

55+ years

Phase:

PHASE1

Brief Summary

The main purpose of the study is to find out if, after 4 weeks of dosing, signs of the investigational drug AGG-523, or its effects, can be measured in urine, blood, or the knee joint. A secondary pur...

Detailed Description

This is a multicenter study of 2 dosing regimens of AGG-523, an investigational aggrecanase inhibitor that is taken orally. Potential study subjects are those with severe Osteoarthritis (OA) of the kn...

Eligibility Criteria

Inclusion

  • Generally healthy, men or women, at least 55 years old
  • Osteoarthritis of the knee requiring total knee replacement surgery

Exclusion

  • Other types of arthritis, like rheumatoid arthritis
  • Recent major surgery (in past 3 months)
  • Recent knee injections (in past 6 months)

Key Trial Info

Start Date :

May 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2008

Estimated Enrollment :

2 Patients enrolled

Trial Details

Trial ID

NCT00454298

Start Date

May 1 2007

End Date

March 1 2008

Last Update

July 29 2009

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Boston, Massachusetts, United States, 02120

2

Boston, Massachusetts, United States, 02215

3

Newton, Massachusetts, United States, 02462

4

Winchester, Massachusetts, United States, 01801

Study Evaluating AGG-523 in Subjects With Severe Osteoarthritis Requiring Total Knee Replacement | DecenTrialz