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Final Analysis of Phase 2 GRIFFIN Study Presented for DARZALEX® (daratumumab)-based Investigational Quadruplet Regimen in Patients with Newly Diagnosed, Transplant-Eligible Multiple Myeloma

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson announced today the final results from the randomized Phase 2 GRIFFIN study.

United statesBortezomib melphalanDouglasw sborovVelcade melphalanVelcade bortezomib melphalanImran khanChristie corbettMyeloma programJanssen biotech incUniversity of utahJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonNational library of medicineEuropean myeloma networkAmerican cancer society

Final Analysis of Phase 2 GRIFFIN Study Presented for DARZALEX® (daratumumab)-based Investigational Quadruplet Regimen in Patients with Newly Diagnosed, Transplant-Eligible Multiple Myeloma

Data featured in plenary session at the 19th International Myeloma Society Annual Meeting LOS ANGELES, Aug. 27, 2022 /PRNewswire/ The Janssen P.

United statesBortezomib melphalanDouglasw sborovVelcade melphalanVelcade bortezomib melphalanImran khanChristie corbettMyeloma programJanssen biotech incUniversity of utahJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonNational library of medicineEuropean myeloma networkAmerican cancer society

Final Analysis of Phase 2 GRIFFIN Study Presented for DARZALEX® (daratumumab)-based Investigational Quadruplet Regimen in Patients with Newly Diagnosed, Transplant-Eligible Multiple Myeloma

Final Analysis of Phase 2 GRIFFIN Study Presented for DARZALEX® (daratumumab)-based Investigational Quadruplet Regimen in Patients with Newly Diagnosed, Transplant-Eligible Multiple Myeloma
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United statesBortezomib melphalanDouglasw sborovVelcade melphalanVelcade bortezomib melphalanImran khanChristie corbettMyeloma programJanssen biotech incUniversity of utahJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonNational library of medicineEuropean myeloma networkAmerican cancer society

Janssen Marks First Approval Worldwide for TECVAYLI?(teclistamab) with EC Authorisation of First-in-Class Bispecific Antibody for the Treatment of Patients with Multiple Myeloma

Teclistamab, an off-the-shelf (ready to use) subcutaneously administered therapy, induced deep and rapid responses in triple-class exposed patients with relapsed and refractory multiple myeloma1 The

United statesJenni mildonWilliamn haitMaria victoria mateosPeter lebowitzEdmond chanNone of the janssen pharmaceutical companiesAmerican society of clinical oncologyEuropean commissionGlobal public healthJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonExchange commissionUniversity hospital of salamancaCompanies of johnson

Janssen Receives Positive CHMP Opinion for Novel Bispecific Antibody TECVAYLI (teclistamab) for the Treatment of Patients with Relapsed and Refractory Multiple Myeloma (RRMM)

Teclistamab is the first T-cell redirecting bispecific antibody to receive a positive CHMP opinion for adults with RRMM and highlights Janssen's commitment to innovation in multiple myeloma The

United statesJenni mildonEdmond chan mbchPeter lebowitzNone of the janssen pharmaceutical companiesAmerican society of clinical oncologyEuropean commissionDrug administrationCancer research instituteJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonExchange commissionCompanies of johnsonEuropean medicines agencyCommittee for medicinal products human use