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March 10, 2022
Out of the 40 patients who enrolled into the ABX464 maintenance study, 23 patients have now reached the first year of treatment and all achieved at least an ACR20 [1] , with 19 and 12 patients achieving
December 1, 2021
End-of-phase-2 response from the US regulatory agency (FDA) provides guidance and a path forward to advance ABX464 into a phase 3 clinical program in ulcerative colitis (UC)PARIS, FRANCE / ACCESSWIRE /
October 18, 2021
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 efficacyFavorable safety and tolerability
August 18, 2021
Guten Morgen mit Abivax SFC Energy Zur Rose Gruppe Epigenomics ... [pic1] Abivax erhรคlt Genehmigung fรผr Phase-1-Studie ABX464 an japanischen Probanden Emmi konstant positiver Entwicklung Rose-Gruppe beschleunigt Wachstum im zweiten Quartal Umsatzplus von 26% AG: Abschluss Biobank
May 27, 2021
Once-daily oral treatment was well-tolerated and demonstrated a good safety profile in Phase IIb study - News - PharmaTimes