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    Home > Active Ingredient News > Digestive System Information > Lancet Gastroent Hepatol: BI 695501, a potential new treatment option for Crohn's disease!

    Lancet Gastroent Hepatol: BI 695501, a potential new treatment option for Crohn's disease!

    • Last Update: 2021-08-27
    • Source: Internet
    • Author: User
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    BI 695501 is a biological generic, in rheumatoid arthritis showed the Adalimumab reference product similar efficacy, safety, and chronic plaque psoriasis patients immunized immunogenic


    BI 695501 is a biological generic, in rheumatoid arthritis showed the Adalimumab reference product similar efficacy, safety, and chronic plaque psoriasis patients immunized immunogenic rheumatoid arthritis immunity

    This is a randomized, double-blind phase 3 trial conducted in 92 centers in 12 countries, recruiting 18-80-year-old patients with moderate to severe active Crohn’s disease (Crohn’s disease activity index [CDAI] score 220 -450 points)


    Remission of each group

    Remission of each group

    From January 4, 2017 to April 5, 2018, a total of 147 patients were recruited and randomly assigned to the BI 695501 group (n=72) or the Adalimumab group (n=75)


    At week 4, 61 (90%) of 68 patients in the BI 695501 group and 68 (94%) of 72 patients in the adalimumab group achieved clinical remission (adjusted RR 0.


    The occurrence of adverse events in each group

    The occurrence of adverse events in each group

    In the safety analysis department, 63% (45/72) and 56% (42/75) of the patients in the BI 695501 group and the adalimumab group had adverse events in the first 24 weeks; week 24-56, Adverse events occurred in 43% and 45% of patients in the two groups, respectively


    In the BI 695501 group and adalimumab group, 63% (45/72) and 56% (42/75) of the patients had adverse events in the first 24 weeks, respectively; in the 24-56 week, 43% and 56% of the patients in the two groups had adverse events.


    There were 6 cases (8%) and 8 cases (11%) of serious adverse events in the BI 695501 group and adalimumab group respectively in the first 24 weeks, and 2 cases (3%) and 9 cases occurred in the 24-56 week period.


    Compared with the reference product of adalimumab, the safety and efficacy of BI 695501 for patients with Crohn's disease are similar.


    Original source:

    Stephen Hanauer, et al.


    Safety and efficacy of BI 695501 versus adalimumab reference product in patients with advanced Crohn's disease (VOLTAIRE-CD): a multicentre, randomised, double-blind, phase 3 trial

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