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New Data for Genentech s Columvi and Lunsumio Presented at ASH 2023 Support Continued Benefit for People With Lymphoma

New Data for Genentech s Columvi and Lunsumio Presented at ASH 2023 Support Continued Benefit for People With Lymphoma
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South san franciscoUnited statesBruno eschliLoren kalmCem mangirKristen ingramLevi garrawayAmerican society of hematologyPhase ibGlobal product developmentRoche groupAmerican societyAnnual meetingGlobal productCytokine release syndromeColumvi patient wallet card

FDA Approves Genentech s Columvi, the First and Only Bispecific Antibody With a Fixed-Duration Treatment for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma | Business

SOUTH SAN FRANCISCO, Calif. (BUSINESS WIRE) Jun 15, 2023

South san franciscoUnited statesKrish patelLoren kalmCem mangirLindsey mathiasInformationandmedication guideorBruno eschliLevi garrawayGenentech access solutionsDrug administrationGlobal product developmentRoche groupSwedish cancer institute in seattleLymphoma programGlobal product

FDA Approves Genentech s Columvi, the First and Only Bispecific Antibody With a Fixed-Duration Treatment for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma

- Pivotal study showed durable responses, with a 56% overall response rate, a 43% complete response (remission) rate, and a median duration of response of 1.5 years (18.4 months) - - Given over

United statesSouth san franciscoBruno eschliLoren kalmLindsey mathiasLevi garrawayKrish patelCem mangirSwedish cancer institute in seattleLymphoma programDrug administrationGenentech access solutionsGlobal product developmentRoche groupGlobal productSwedish cancer institute

FDA Approves Genentech s Columvi, the First and Only Bispecific Antibody With a Fixed-Duration Treatment for People With Relapsed or Refractory Diffuse Large B-cell Lymphoma | Region

SOUTH SAN FRANCISCO, Calif. (BUSINESS WIRE) Jun 15, 2023

United statesSouth san franciscoLevi garrawayKrish patelLindsey mathiasInformationandmedication guideorLoren kalmCem mangirBruno eschliGlobal product developmentDrug administrationRoche groupLymphoma programGenentech access solutionsSwedish cancer institute in seattleGlobal product

FDA Approves Genentech s Polivy in Combination With R-CHP for People With Certain Types of Previously Untreated Diffuse Large B-cell Lymphoma

– Polivy combination is the first FDA-approved therapy in nearly 20 years for the first-line treatment of diffuse large B-cell lymphoma, an aggressive disease and the most common form of non-Hodgkin’s lymphoma in the U.S. –– POLARIX trial showed the Polivy combination reduced the risk of disease progression, relapse.

United statesSouth san franciscoBruno eschliLoren kalmLevi garrawayCem mangirLymphoma academic research organisationRoche groupLymphoma study associationGlobal product developmentDrug administrationInternational prognostic indexGlobal productLugano response criteriaPrescribing informationImportant safety