Study Evaluating Long-Term Safety Of ATN-103 In Subjects With Rheumatoid Arthritis
Status: | Completed |
---|---|
Conditions: | Arthritis, Rheumatoid Arthritis |
Therapuetic Areas: | Rheumatology |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 4/21/2016 |
Start Date: | February 2010 |
End Date: | February 2012 |
An Open-Label Extension Study To Assess The Long-term Safety And Tolerability Of ATN-103 In Subjects With Rheumatoid Arthritis
This open-label extension study will allow subjects who have completed either the
3242K1-2000-WW or 3242K1-2001-JA study to receive up to an additional 48 weeks of ATN-103
treatment and will provide data on the long-term safety and tolerability of ATN-103 in
subjects with rheumatoid arthritis.
3242K1-2000-WW or 3242K1-2001-JA study to receive up to an additional 48 weeks of ATN-103
treatment and will provide data on the long-term safety and tolerability of ATN-103 in
subjects with rheumatoid arthritis.
Inclusion Criteria:
- Subjects must have completed study 3242K1-2000-WW or 3242K1-2001-JA and have had no
events that, in the opinion of the investigator, would preclude entry or
participation in this study.
Exclusion Criteria:
- Pregnant or nursing women.
- Any major illness/condition or evidence of an unstable clinical condition (eg, renal,
hepatic, cardiovascular, hematological, gastrointestinal, endocrine, pulmonary,
immunologic [eg, Felty syndrome, human immunodeficiency virus (HIV) infection],
infectious, neurological, or cerebral psychiatric disease, or evidence of
demyelinating disease) that, in the investigator's judgment, will substantially
increase the risk associated with the subject's developing an adverse event (AE) or
serious adverse event (SAE) during the study, or preclude the evaluation of the
subject's response.
We found this trial at
26
sites
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