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Johnson & Johnson : CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy

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United statesRegion flamandeEdmond chanJenni mildonCiltacabtagene autoleucelEuropean commission grants conditional approvalLegend biotech united states incJanssen biotech incDrug administrationAmerican society of clinical oncologyEuropean commissionJanssen cilag internationalChinese company legend biotech to develop investigationalAmerican cancer societyCommittee for orphan medicinal productsJanssen research development

Galapagos NV: Galapagos showcases innovative approach in hematological cancer care with clinical and translational data presentations at EBMT congress 2024

Galapagos NV: Galapagos showcases innovative approach in hematological cancer care with clinical and translational data presentations at EBMT congress 2024
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United kingdomRegion flamandeGlasgow cityValentin ortiz maldonadoLeticia alserawanChristian jacquesSophie servaisKirsten saevelsJeevan shettyClaire venninEva santermansSandra cauwenberghsJoost sp vermaatJo caersMarie josSandra blum

FDA Approval Highlights: OncLive s February Recap

In case you missed it, below is a recap of all drugs that have been approved by the FDA in February 2024.

University of chicagoUnited statesLos angelesDana farber cancer instituteNew havenDavidm livingstonDaniel olsonHarriet klugerRachel kobosZeva wainbergUniversity of californiaTranslational researchLowe centerEuropean commissionOncology research developmentChen huang center

FDA Accepts Priority Review for Linvoseltamab to Treat Adult Patients With R/R MM

Currently, the safety and efficacy of linvoseltamab in adult patients with relapsed or refractory multiple myeloma is being compared to elotuzumab, pomalidomide, and dexamethasone in a phase 3 clinical trial.

Jo panuwatRegeneron pharmaceuticalsRefractory multiple myeloma accepted forAcceptance for treatmentRefractory multipleLearn how well linvoseltamab works comparedAdult participants withRefractory multiple myeloma

TECVAYLI® (teclistamab-cqyv) biweekly dosing approved by the U S FDA for the treatment of patients with relapsed or refractory multiple myeloma

TECVAYLI® (teclistamab-cqyv) biweekly dosing approved by the U S FDA for the treatment of patients with relapsed or refractory multiple myeloma
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United statesSatu glaweRachel kobosChristie corbettPrnewswire johnsonNational cancer instituteExchange commissionDrug administrationOncology research developmentOther administration reactionsJanssen research developmentJohnson incSurveillance research programJanssen biotech incAmerican cancer societyAmerican society of clinical oncology