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NCT05421442: DANBIO

A Post-marketing Study on the Safety of Abatacept Treatment in Denmark Using the Danish Database

Completed Last updated 8 December 2025
What this trial tests

trial in Rheumatoid Arthritis (RA) in 38,396 participants. Completed in 31 October 2025.

Timeline
13 June 2019
Primary endpoint
22 August 2025
31 October 2025

Quick facts

Lead sponsorBristol-Myers Squibb
StatusCompleted
Study typeOBSERVATIONAL
Enrollment38,396
Start date13 June 2019
Primary completion22 August 2025
Estimated completion31 October 2025
Sites1 location across United States

Conditions studied

Sponsor

Bristol-Myers Squibb — full company profile →

Who can join

18 and older, any sex, with Rheumatoid Arthritis (RA) or Psoriatic Arthritis (PsA). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to expand on the ongoing post-marketing monitoring of abatacept to include all participants with rheumatoid arthritis (RA) and psoriatic arthritis (PsA) treated with abatacept captured in Danish Database for Biologic Therapies (DANBIO).

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Rheumatoid Arthritis (RA)

Currently open trials in the same condition.

Other Bristol-Myers Squibb trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05421442.

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