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A Randomized, Double-Blind, Placebo-Controlled 52-Week Study to Assess Adverse Events of Special Interest in Adults With Active, Autoantibody-Positive Systemic Lupus Erythematosus Receiving Belimumab

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A Randomized, Double-Blind, Placebo-Controlled 52-Week Study to Assess Adverse Events of Special Interest in Adults With Active, Autoantibody-Positive Systemic Lupus Erythematosus Receiving Belimumab

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 22 Jul 2024

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At a glance

  • Drugs Belimumab (Primary)
  • Indications Systemic lupus erythematosus
  • Focus Adverse reactions
  • Acronyms BASE
  • Sponsors GlaxoSmithKline; GSK; Human Genome Sciences

    • Most Recent Events

    • 15 Nov 2023 Results assessing the incidence of infections onbelimumab treatment summarized 52-week infection data from BASE study and BEL116559 which is a pooled post hoc analysis of six studies (BEL110751, BEL110752, BEL112341, BEL113750, BEL115471 and LBSL02) presented at the ACR Convergence 2023.
    • 15 Nov 2023 Results assessing of 5-year safety of belimumab therapy in patients with Systemic Lupus Erythematosus, presented at the ACR Convergence 2023.
    • 24 Nov 2022 Status changed from active, no longer recruiting to completed.

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