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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

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

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

/PRNewswire/ Johnson & Johnson announced today that the U.S. Food and Drug Administration (FDA) has approved the supplemental Biologics License Application.

United statesChristie corbettRachel kobosPrnewswire johnsonSatu glaweNational cancer instituteEuropean commissionAmerican society of clinical oncologyExchange commissionAmerican cancer societyOncology research developmentOther administration reactionsSurveillance research programJohnson incJanssen biotech incNone of janssen research development

U S FDA Approves TALVEY™ (talquetamab-tgvs), a First-in-Class Bispecific Therapy for the Treatment of Patients with Heavily Pretreated Multiple Myeloma

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson announced today that the U.S. Food and Drug Administration (FDA) has granted.

United statesSan franciscoMichael andreiniCaroline pavisObrian kenneyPeter lebowitzExchange commissionUniversity of californiaJanssen pharmaceutical companies of johnsonJanssen biotech incMyeloma programEuropean commissionCompanies of johnsonNational cancer instituteNone of the janssen pharmaceutical companiesEastern cooperative oncology group