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Lynozyfic™ (linvoseltamab) Monotherapy in Newly Diagnosed Multiple Myeloma (NDMM) Shows Impressive Responses, Supporting Rationale as a Potential Foundation in Frontline Treatment

All three dose groups (50 mg, 100 mg and 200 mg) showed impressive monotherapy efficacy, with VGPR+ (very good partial response or better) of ≥70% despite limited follow-up; evidence shows that these responses are expected to deepen over time Across all dose groups, 95% (19 of 20 patients) of all evaluable VGPR+ patients achieved minimal residual disease negative status Data featured in an ASH oral presentation; LINKER-MM4 is the first clinical trial to evaluate a BCMAxCD3 bispecific monotherapy

articleRegeneron Pharmaceuticals, Inc.December 7, 202516/company/regeneron-pharmaceuticals-inc/news/lynozyfictm-linvoseltamab-monotherapy-in-newly-diagnosed-multiple-myeloma-ndmm-shows-impressive-responses-supporting-rationale-as-a-potential-foundation-in-frontline-treatment
Lynozyfic™ (linvoseltamab) Monotherapy in Newly Diagnosed Multiple Myeloma (NDMM) Shows Impressive Responses, Supporting Rationale as a Potential Foundation in Frontline Treatment

About this update from Regeneron Pharmaceuticals, Inc.

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