Overview

SPRiNG: SCIO-469 Patients With Rheumatoid Arthritis Not Receiving Methotrexate

Status:
Completed
Trial end date:
2005-10-01
Target enrollment:
0
Participant gender:
All
Summary
The primary objective of this study is to determine the efficacy of oral SCIO-469 in patients with rheumatoid arthritis who are not receiving liver damaging (hepatotoxic) disease-modifying anti-rheumatic drugs (DMARDs).
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Scios, Inc.
Treatments:
Methotrexate
Criteria
Inclusion Criteria:

- Patients having active rheumatoid arthritis who are not receiving medications known as
hepatotoxic disease-modifying anti-rheumatic drugs (DMARDs)

- Patients taking hydroxychloroquine (Plaquenil) must be on a stable or consistent dose
prior to entering study

Exclusion Criteria:

- Patients using Enbrel, Remicade, Kineret, Humira, or an experimental biologic agent
within the past 3 months

- Lab tests revealed elevated liver enzymes within the past 6 months

- Medical history of Tuberculosis, cancer, multiple sclerosis, neuropathy or
encephalopathy

- HIV positive

- Abnormal electrocardiogram

- Chronic or acute infection