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Impressive clinical remission in 58.4% (ITT) of 101 patients after 48 weeks of once-daily oral 50mg ABX464, showing both maintained as well as further improved efficacy
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Favorable safety and tolerability profile continues to support ABX464 chronic use potential
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Launch of global phase 3 program with ABX464 in ulcerative colitis in preparation, with end-of-Phase-2 US FDA meeting in Q4 2021 and EMA Scientific Advice in early Q1 2022
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Abivax’s late-breaking abstract presentation and Live Industry Symposium at UEG Week Virtual 2021 now publicly available