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AbbVie Reports Positive Phase 3 CERVINO Results for Etentamig

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Sig2.88Sen+6.21Env0.00Soc+2.35Gov+0.64

Etentamig, AbbVie’s investigational BCMA x CD3 bispecific, showed significantly improved outcomes in the Phase 3 CERVINO trial versus standard available therapies in triple-class exposed relapsed/refractory multiple myeloma. Objective response rate was 74%, with a hazard ratio of 0.40 for progression-free survival. AbbVie highlights a manageable safety profile, convenient dosing, and potential for outpatient, community-based care to improve access.

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