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Bristol Myers Squibb Announces Up to Five Years of Data from Long-Term DAYBREAK Study Reinforcing Efficacy and Safety Profile of Zeposia in Patients with Relapsing Forms of Multiple Sclerosis

Treatment with Zeposia demonstrated a low annualized relapse rate of 0.103 and more than 70% of patients were relapse-free at four years Safety was consistent with prior findings and the established safety profile of Zeposia in up to 5 years of follow-up Bristol Myers Squibb today announced interim results from the Phase 3 open-label extension trial DAYBREAK, demonstrating the long-term efficacy and safety profile ...
Sarah Harris Bruce Cree Anna Castelo Branco Sonia Afsari Nina Goworek Jonathan Sadeh

Bristol Myers Squibb Presents New Data at Digestive Disease Week® on Zeposia (ozanimod) Highlighting Clinical Benefits and Safety Profile in Patients with Ulcerative Colitis

Bristol Myers Squibb (NYSE:BMY) today announced that additional data from multiple studies evaluating Zeposia (ozanimod) in ulcerative colitis (UC) were presented at Digestive Disease Week ® (DDW), taking place virtually May 21-23, 2021. These data deepen the understanding of Zeposia and reinforce Bristol Myers Squibb’s commitment to understanding and addressing unmet needs in gastroenterology. Research being shared includes: Safety of Ozanimod in Patients with Moderately to Severely ...
United States Mary Beth Harler Bristol Myers Squibb American Society For Gastrointestinal Endoscopy Bristol Myers Squibb Company Health Economics

Bristol Myers Squibb Presents Positive Data from Two Pivotal Phase 3 Psoriasis Studies Demonstrating Superiority of Deucravacitinib Compared to Placebo and Otezla®

Bristol Myers Squibb Presents Positive Data from Two Pivotal Phase 3 Psoriasis Studies Demonstrating Superiority of Deucravacitinib Compared to Placebo and Otezla® Significantly more patients treated with deucravacitinib achieved PASI 75 and sPGA 01 compared to patients treated with placebo and Otezla at Week 16, with an increased benefit versus Otezla at Week 24 and maintained through Week 52 Deucravacitinib was well tolerated with a low rate of discontinuation due to adverse events Deucravac...
United States April Armstrong Kirby Hosea Nina Goworek Mary Beth Harler Bristol Myers Squibb

Bristol Myers Squibb: EMA Validates Marketing Authorization Application For Zeposia

Bristol Myers Squibb: EMA Validates Marketing Authorization Application For Zeposia NEW YORK CITY (dpa-AFX) - Bristol Myers Squibb (BMY) said the European Medicines Agency has validated its Marketing Authorization Application for Zeposia for the treatment of adults with moderately to severely active ulcerative colitis. This confirms the submission is complete and begins the EMAs centralized review process. Mary Beth Harler, head of Immunology and Fibrosis Development, Bristol Myers Squibb, said...
Mary Beth Harler Bristol Myers Squibb European Union European Medicines Agency Fibrosis Development Myers Squibb

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