BMS's iza-bren shows significant survival benefit in two cancers
The dual-targeted ADC met primary endpoints in two Phase 3 trials, showing statistically significant OS and PFS improvements.
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Global biopharmaceutical company
bms.comLast updated
In short: BMS reported strong Q1 2026 financial growth and achieved several regulatory milestones, including European approval for Sotyktu and Opdivo.
The dual-targeted ADC met primary endpoints in two Phase 3 trials, showing statistically significant OS and PFS improvements.
If approved, it would be the first pharmacological therapy for adolescent oHCM with a safety profile similar to adults.
The first immunotherapy regimen approved in Europe for frontline advanced classical Hodgkin lymphoma in adults and adolescents aged 12 and older.
The PD-L1xVEGF-A bispecific showed high response rates across subtypes and PD-L1 levels in ROSETTA Lung-02.
About Bristol Myers Squibb: ... At Bristol Myers Squibb, our mission is to discover, develop and deliver innovative medicines that help patients prevail over serious...
Bristol-Myers Squibb (BMY) stock is drawing attention after recent trading performance, with shares closing at US$55.28.
Bristol Myers Squibb (BMS) has revealed clinical data for two pipeline candidates in multiple myelom...
Bristol Myers Squibb’s supplemental new drug application (sNDA) for sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis accepted for review across four...
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