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NCT01095393

National Data Bank for Rheumatic Disease Registry Study of Safety in Patients With Rheumatoid Arthritis Treated With Cimzia® or Disease-modifying Antirheumatic Drugs (DMARDs)

Completed Last updated 16 July 2020
What this trial tests

trial in Rheumatoid Arthritis in 12,500 participants. Completed in 31 December 2019.

Timeline
1 September 2009
Primary endpoint
13 December 2016
31 December 2019

Quick facts

Lead sponsorUCB Pharma
StatusCompleted
Study typeOBSERVATIONAL
Enrollment12,500
Start date1 September 2009
Primary completion13 December 2016
Estimated completion31 December 2019

Conditions studied

Sponsor

UCB Pharma — full company profile →

Who can join

Eligibility, any sex, with Rheumatoid Arthritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Observational registry to assess the longer-term risk of serious infections and malignancies reported with TNFα-blocker therapy, as well as the longer-term risk of cardiovascular and thromboembolic events in adult Rheumatoid Arthritis (RA) patients treated with Cimzia® as compared to non-biologic DMARD-treated controls.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Rheumatoid Arthritis

Currently open trials in the same condition.

Other UCB Pharma trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01095393.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing