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CERVINO

PharmaDeviceNews CERVINO
Representative image: CARVYKTI multiple myeloma treatment setting as Legend Biotech reports five-year progression-free survival after a single CAR T-cell infusion.
Pharma & Biotech

AbbVie submits FDA application for etentamig after Phase 3 CERVINO success in multiple myeloma

AbbVie seeks FDA approval for etentamig after Phase 3 myeloma results showed a 60% reduction in progression risk. Infection safety remains in focus.

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AbbVie is positioning etentamig as a monthly BCMA-directed bispecific treatment for heavily pretreated multiple myeloma patients. Representative image.
Pharma & Biotech

AbbVie’s etentamig cuts myeloma progression risk 60% as monthly bispecific strategy nears its real test

AbbVie will present full Phase 3 CERVINO data for etentamig after the BCMA bispecific produced a 74% response rate and reduced progression or death risk by 60% in heavily pretreated multiple myeloma.

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AbbVie’s etentamig delivered strong Phase 3 efficacy in relapsed multiple myeloma while its monthly dosing strategy could broaden access to BCMA-directed bispecific therapy. Representative image.
Features & Analysis

AbbVie’s second-generation BCMA bispecific succeeded in Phase 3. What makes CERVINO commercially important?

AbbVie’s etentamig delivered a 74% response rate and reduced the risk of progression or death by 60% in the Phase 3 CERVINO trial. Its real competitive proposition, however, may be operational: monthly dosing after a single step-up dose could help move BCMA-directed T-cell therapy beyond specialist centres.

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