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Completed

NCT Number: NCT02885818

Does Abatacept Induce Regulatory B Cells in Patients With Rheumatoid Arthritis

Abatacept disrupts T-cell coactivation signals in rheumatoid arthritis (RA). Its potential effects on B cells are not well described. This study will assess the effects of abatacept therapy on the phenotype and function of peripheral blood B cells in patients with RA.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • RA as defined by ACR/EULAR criteria
  • Clinical indication to start abatacept therapy

Exclusion criteria

  • Treatment by rituximab in the previous year

Treatment and study plan

Primary outcomes

  1. Peripheral blood B-cell phenotype changes

    Time frame: 3 months

    Measure of the proportion of the main B-cell subsets (transitional, naïve, memory, plasmablasts) by FACS analysis before abatacept initiation and 3 months later.

Secondary outcomes

  1. In vitro B-cell function and regulatory properties

    Time frame: 3 months

    In vitro culture of B cells from the patients to assess B cell inhibition of T cell proliferation before abatacept initiation and 3 months later.

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Acronym: ABATACEPT_B

Important dates

Study start
2014
Primary completion
2018
Study completion
2018
First posted
Sep 1, 2016
Registry last updated
Apr 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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