Overview

Study To Evaluate The Pharmacokinetic Interaction Between PLA-695 And Methotrexate In Adults With Rheumatoid Arthritis

Status:
Completed
Trial end date:
2007-11-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine if PLA-695 changes the blood concentrations of methotrexate when administered together.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Treatments:
Methotrexate
Criteria
Inclusion Criteria:

- Men or women of nonchildbearing potential with rheumatoid arthritis (RA), aged 18 to
75 years

- RA disease onset after 16 years of age and has had the disease for at least 6 months

- Must be receiving a stable, well-tolerated oral dose of methotrexate (5 to 25 mg)
taken once weekly for at least 3 months

Exclusion Criteria:

- Evidence of unstable clinically significant disease