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LUMAKRAS™ (Sotorasib) Combined With Vectibix® (Panitumumab) Showed Encouraging Efficacy And Safety In Patients With KRAS G12C-Mutated Colorectal Cancer

/PRNewswire/ Amgen (NASDAQ: AMGN) today announced the first combination study results from the Phase 1b/2 CodeBreaK 101 study, the most comprehensive global.

United arab emiratesHong kongUnited kingdomPuerto ricoSouth koreaGreat britainMegan foxTrish rowlandStevens johnsonMarwang fakihVan cutsemDavidm reeseKyowa kirin co ltdEuropean society of medical oncologyWorld health organizationDrug administration

LUMAKRAS Combined With Vectibix® Showed Encouraging Efficacy And Safety In Patients With KRAS G12C-Mutated Colorectal Cancer

LUMAKRAS Combined With Vectibix® Showed Encouraging Efficacy And Safety In Patients With KRAS G12C-Mutated Colorectal Cancer
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United arab emiratesHong kongUnited kingdomPuerto ricoSouth koreaGreat britainMegan foxTrish rowlandStevens johnsonMarwang fakihVan cutsemDavidm reeseKyowa kirin co ltdEuropean society of medical oncologyWorld health organizationDrug administration

Health Canada approves LUMAKRAS™ (sotorasib), the first and only targeted treatment for patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer

Health Canada approves LUMAKRAS™ (sotorasib), the first and only targeted treatment for patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer
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EMA Validates Bristol Myers Squibb s Applications for Opdivo (nivolumab) + Yervoy (ipilimumab) and Opdivo + Chemotherapy as First-Line Treatments for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

EMA Validates Bristol Myers Squibb s Applications for Opdivo (nivolumab) + Yervoy (ipilimumab) and Opdivo + Chemotherapy as First-Line Treatments for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
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United statesSouth koreaIanm waxmanNina goworekBristol myers squibbCompany opdivoAmerican society of clinical oncologyDrug administrationBristol myers squibb companyExchange commissionOno pharmaceutical coEuropean unionEuropean medicines agencyMyers squibbMarketing authorization applicationsBristol myers

EMA Validates Bristol Myers Squibb s Applications for Opdivo + Yervoy and Opdivo + Chemotherapy as First-Line Treatments for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

Applications based on positive results from the Phase 3 CheckMate -648 trial, in which both Opdivo -based combinations demonstrated a significant survival benefit over chemotherapy alone Bristol Myers Squibb today announced that the European Medicines Agency has validated its Type II Variation Marketing Authorization Applications for both Opdivo in combination with Yervoy and Opdivo in combination with .

United statesSouth koreaIanm waxmanNina goworekBristol myers squibbCompany opdivoAmerican society of clinical oncologyDrug administrationBristol myers squibb companyExchange commissionOno pharmaceutical coEuropean unionEuropean medicines agencyMyers squibbMarketing authorization applicationsBristol myers