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BioPharma Dive·2h ago·1 min read
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AbbVie/Genmab’s Epkinly halves progression risk in frontline DLBCL trial

Oct 6, 2026·read at BioPharma Dive ↗Positive readoutPositive

A Phase 3 study of the bispecific antibody Epkinly combined with standard chemotherapy showed nearly a 50% reduction in the risk of disease progression or death compared with chemotherapy alone in patients with newly diagnosed diffuse large B‑cell lymphoma (DLBCL).\n\nThe results exceeded analyst expectations, outperformed a competing Roche regimen, and position Epkinly to become the first bispecific therapy approved for first‑line treatment of DLBCL.\n\nGenmab, which shares ownership of Epkinly with AbbVie, reported $312 million in global net sales of the drug in the first half of the year, and its shares rose as much as 14% after the data were released.\n\nThe trial adds to a growing portfolio of bispecific antibodies that are reshaping care for blood cancers by linking diseased B cells to T cells to trigger an immune response.

source

This writeup was produced by pharmadog from original reporting by BioPharma Dive.

Original headline: “Dual-acting drug from AbbVie, Genmab scores in frontline lymphoma trial”

read at BioPharma Dive ↗
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companies & drugs in this story

companies
ABBVIE6ROCHE4ASTRAZENECA
drugs
EPKINLY14epcoritamab14CALQUENCELUNSUMIOPOLIVYmosunetuzumabpolatuzumab vedotin
topics
Bispecific Antibody6DLBCL6Immunology3Monoclonal Antibody3Approval2Hematology2Oncology2

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