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Johnson & Johnson : advances leadership in oncology innovation with more than 75 clinical study and real-world presentations at ASCO and EHA

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South koreaUnited statesYusri elsayedBiljana naumovicChristie corbettSatu glaweEuropean hematology associationOncologic drugs advisory committeeNational comprehensive cancer networkLegend biotech united states incDrug administrationJanssen biotech incA us national healthcare claims analysisJanssen pharmaceuticalsEuropean myeloma networkEuropean commission

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

Johnson & Johnson's bone cancer drug gets USFDA nod - Pharma News

Johnson & Johnson's bone cancer drug gets USFDA nod - Pharma News
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United statesBinod dhakalLegend biotech united states incDrug administrationJapan ministry of healthCollege of wisconsinDivision of hematologyJanssen biotech incAssociate professorMedical collegeJordan schecterJohnson innovativeJanssen biotechLegend biotech united states

CARVYKTI® is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy

CARVYKTI® is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy
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United statesHemophagocytic lymphohistiocytosisTyrone brewerSatu glaweBinod dhakalCommittee for medicinal products human useLegend biotech united states incDrug administrationJanssen research developmentJanssen biotech incExchange commissionOncologic drugs advisory committeeCollege of wisconsinNational cancer instituteJapan ministry of healthAmerican cancer society

Johnson & Johnson: CARVYKTI is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy

Johnson & Johnson: CARVYKTI is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy
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United statesTyrone brewerBinod dhakalPrnewswire johnsonSatu glaweDennis riedlHemophagocytic lymphohistiocytosisCommittee for medicinal products human useAmerican society of clinical oncologyJanssen biotech incOncologic drugs advisory committeeJanssen research developmentExchange commissionNational cancer instituteAmerican cancer societyDrug administration