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Astellas XTANDI™ (Enzalutamide) Granted European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting

/PRNewswire/ Astellas Pharma Inc. (TSE: 4503, President and CEO: Naoki Okamura, "Astellas") today announced the European Commission (EC) has approved a.

United statesComunidad autonoma de catalunaAntonio alcarazAhsan arozullahEuropean unionDrug administrationEuropean association of urologyEuropean commissionDepartment of urologyAmerican society of clinical oncologyUniversity hospital clinic of barcelonaCommittee for medicinal products human useEuropean medicines agencyAstellas pharma incPrnewswire astellas pharma incHead of oncology development

Astellas XTANDItm (Enzalutamide) Granted European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting

Astellas XTANDItm (Enzalutamide) Granted European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting
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Comunidad autonoma de catalunaUnited statesAhsan arozullahAntonio alcarazAmerican society of clinical oncologyEuropean medicines agencyPrnewswire astellas pharma incEuropean commissionCommittee for medicinal products human useHead of oncology developmentEuropean association of urologyUniversity hospital clinic of barcelonaDepartment of urologyDrug administrationEuropean unionAstellas pharma inc

Astellas XTANDI™ (Enzalutamide) Granted European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting

Astellas XTANDI™ (Enzalutamide) Granted European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting
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Comunidad autonoma de catalunaUnited statesAntonio alcarazAhsan arozullahDrug administrationUniversity hospital clinic of barcelonaEuropean medicines agencyEuropean unionCommittee for medicinal products human useAmerican society of clinical oncologyHead of oncology developmentEuropean association of urologyEuropean commissionDepartment of urologyPrnewswire astellas pharma incAstellas pharma inc

Pfizer (PFE) Announces EMA Validates Type II Variation Application for PADCEV with KEYTRUDA for First-Line Treatment of Advanced Bladder Cancer

Pfizer (PFE) Announces EMA Validates Type II Variation Application for PADCEV with KEYTRUDA for First-Line Treatment of Advanced Bladder Cancer
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Ahsan arozullahNaoki okamuraRoger danseyAstellas pharma incEuropean society for medical oncologyCommittee for medicinal products human useHead of oncology developmentPfizer incEuropean medicines agencyDrug administrationEuropean commissionAstellas pharmaChief development officerSenior vice presidentOncology developmentMedicinal products

European Medicines Agency Validates Type II Variation Application for PADCEV® (enfortumab vedotin) with KEYTRUDA® (pembrolizumab) for First-Line Treatment of Advanced Bladder Cancer

European Medicines Agency Validates Type II Variation Application for PADCEV® (enfortumab vedotin) with KEYTRUDA® (pembrolizumab) for First-Line Treatment of Advanced Bladder Cancer
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United statesNaoki okamuraAhsan arozullahRoger danseyDrug administrationEuropean society for medical oncologyInternational agency for research on cancerMerck sharp dohme corpAstellas pharma us incMerck co incEuropean commissionCorporate communicationsEuropean medicines agency for padcevNational cancer institutePfizer incHead of oncology development