Study to Characterize the Pharmacokinetics of a Single Dose of SC Abatacept 125 mg Using the BD Autoinjector or the Prefilled Syringe

Completed · Phase 1

Conditions studied: Rheumatoid Arthritis

In brief

The primary purpose of the protocol is to describe the pharmacokinetics of a single dose of Abatacept 125 mg in Rheumatoid Arthritis patients delivered via the autoinjector device or the approved prefilled syringe.

Key facts

Study ID
NCT01890473
Run by
Bristol-Myers Squibb
People needed
356
Starts
2013-07-01
Expected to finish
2014-11-01
Last updated by the study team
2015-11-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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