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Janssen Announces Unblinding of Phase 3 CARTITUDE-4 Study of CARVYKTI® (cilta-cel) as Primary Endpoint Met in Treatment of Patients with Relapsed and Refractory Multiple Myeloma

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson today announced that the Phase 3 CARTITUDE-4 study evaluating CARVYKTI®.

United statesHemophagocytic lymphohistiocytosisSatu glaweClinical development cellular therapy programNational cancer instituteJanssen biotech incJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonJapan ministry of healthAmerican cancer societyNone of the janssen pharmaceutical companiesDrug administrationEuropean commissionData monitoring committeeExchange commission

Legend Biotech (LEGN) Announces Phase 3 CARTITUDE-4 Study of CARVYKTI Met Its Primary Endpoint

Legend Biotech (LEGN) Announces Phase 3 CARTITUDE-4 Study of CARVYKTI Met Its Primary Endpoint
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United statesNew jerseyHemophagocytic lymphohistiocytosisJoanne choiLida pacaudTina carterAmerican society of clinical oncologyJanssen biotech incExchange commission onEuropean commission for the treatment of patientsJapan ministry of healthLegend biotech corporationCommunity register of orphan medicinal productsClinical developmentAmerican cancer societyDrug administration

Legend Biotech Announces Phase 3 CARTITUDE-4 Study of CARVYKTI (ciltacabtagene autoleucel) Has Met Its Primary Endpoint in the Treatment of Patients with Relapsed and Refractory Multiple Myeloma

27.01.2023 - Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global biotechnology company developing, manufacturing and commercializing novel therapies to treat life-threatening diseases, announced today that CARTITUDE-4, the Phase 3 study .

United statesNew jerseyHemophagocytic lymphohistiocytosisLida pacaudAmerican society of clinical oncologyJanssen biotech incExchange commission onEuropean commission for the treatment of patientsLegend biotech corporation stockJapan ministry of healthCommunity register of orphan medicinal productsClinical developmentAmerican cancer societyDrug administrationEuropean commissionMedicinal devices agency

Janssen Presents Efficacy and Subgroup Analyses from MAIA Study Showing Long-Term Results of DARZALEX® (daratumumab)-based Regimen in Newly Diagnosed, Transplant-Ineligible Multiple Myeloma

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new analyses from the Phase 3 MAIA study of DARZALEX® (daratumumab).

United statesGoldschmidth daratumumabShaji kumarMark wildgustChristie corbettGlobal medical affairsJanssen biotech incAmerican society of hematology annual meetingJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonAmerican society of hematologyDivision of hematologyNational comprehensive cancer networkAmerican cancer societyNone of the janssen pharmaceutical companies

Legend Biotech (LEGN) Announces CARVYKTI Approved in Japan for Treatment of Relapsed or Refractory Multiple Myeloma

Legend Biotech (LEGN) Announces CARVYKTI Approved in Japan for Treatment of Relapsed or Refractory Multiple Myeloma
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United statesNew jerseyHemophagocytic lymphohistiocytosisJoanne choiYing huangTina carterJanssen biotech incExchange commission onAmerican society of clinical oncologyChinese centerEuropean commission for the treatment of patientsJapan ministry of healthLegend biotech corporationJanssen pharmaceuticalsDrug evaluation of national medical products administrationCommunity register of orphan medicinal products