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Opdivo (nivolumab) Plus Yervoy (ipilimumab) Demonstrates Durable Overall Survival at Three Years Compared to Chemotherapy in First-Line Unresectable Malignant Pleural Mesothelioma in Phase 3 CheckMate -743 Trial | Antibodies

Opdivo (nivolumab) Plus Yervoy (ipilimumab) Demonstrates Durable Overall Survival at Three Years Compared to Chemotherapy in First-Line Unresectable Malignant Pleural Mesothelioma in Phase 3 CheckMate -743 Trial | Antibodies
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United statesSouth koreaAbderrahim oukessouIbristol myers squibbSolange petersCompany opdivoBristol myers squibb companyOncology serviceEuropean society for medical oncology virtual congressEuropean unionLausanne university hospitalVirtual congressBristol myers squibbDrug administrationOno pharmaceutical coEuropean society for medical oncology

U S Food and Drug Administration Approves Opdivo® for the Adjuvant Treatment of Patients with High-Risk Urothelial Carcinoma

U S Food and Drug Administration Approves Opdivo® for the Adjuvant Treatment of Patients with High-Risk Urothelial Carcinoma
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United statesSouth koreaMatthewd galskyBristol myers squibbAdam lenkowskyBristol myers squibb companyTime oncology review pilot programTranslational researchAmerican cancer societyNational comprehensive cancer networkTisch cancer instituteDrug administrationExchange commissionUs food drug administrationIcahn school of medicine at mount sinaiOno pharmaceutical co

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

Bristol Myers Squibb Receives European Commission Approval for Opdivo as Adjuvant Treatment for Esophageal or Gastroesophageal Junction Cancer Patients with Residual Pathologic Disease Following Chemoradiotherapy

Bristol Myers Squibb Receives European Commission Approval for Opdivo as Adjuvant Treatment for Esophageal or Gastroesophageal Junction Cancer Patients with Residual Pathologic Disease Following Chemoradiotherapy
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United statesSouth koreaIanm waxmanNina goworekBristol myers squibbCompany opdivoAmerican society of clinical oncologyBristol myers squibb companyEuropean unionVirtual congressDrug administrationEuropean commissionExchange commissionOno pharmaceutical coEuropean society for medical oncologyMyers squibb

Bristol Myers Squibb Provides Update on CheckMate -651 Trial Evaluating Opdivo Plus Yervoy Versus EXTREME Regimen as First-Line Treatment for Squamous Cell Carcinoma of the Head and Neck

Bristol Myers Squibb Provides Update on CheckMate -651 Trial Evaluating Opdivo Plus Yervoy Versus EXTREME Regimen as First-Line Treatment for Squamous Cell Carcinoma of the Head and Neck
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United statesSouth koreaAbderrahim oukessouNina goworekBristol myers squibbCompany opdivoDrug administrationBristol myers squibb companyExchange commissionOno pharmaceutical coEuropean unionEuropean medicines agencyBristol myersMyers squibbBetter futureFatal immune mediated adverse reactions