Study Details

Long-term treatment study of CDP870 self-injection in patients with active rheumatoid arthritis who are participating in the long-term treatment studies (Study 275-08-002 or Study 275-08-004) of CDP870

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT02586246

Astellas Study ID

The unique identification code given by the study sponsor.

1226-CL-A003

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Condition

Rheumatoid Arthritis

Phase

These clinical trials are done to confirm that an experimental treatment helps participants who have a specific condition. These clinical trials often compare the experimental treatment to another treatment or, if appropriate, a placebo.

Phase 3

Age

N/A - N/A

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Jan 2011 - May 2013

Masking

None (Open Label)

Enrollment number

86

Long-term Treatment Study of CDP870 Self-injection. A Multicenter, Open-label, Long-term Safety Study to evaluate the Safety and Efficacy of CDP870 Self-injection administered at a dose of 200 mg biweekly for 24 weeks or longer in Patients with Active Rheumatoid Arthritis who are participating in the Long-term Treatment Studies (Study 275-08-002 or Study 275-08-004) of CDP870 administered concomitantly with or without Methotrexate (MTX)

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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