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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

Astellas VEOZATM (fezolinetant) Approved by European Commission for Treatment of Vasomotor Symptoms Associated with Menopause

Astellas VEOZATM (fezolinetant) Approved by European Commission for Treatment of Vasomotor Symptoms Associated with Menopause
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United statesNaoki okamuraRossella nappiPrzegl menopauzalnyJ public healthHealth qual life outcomesEuropean commissionHead of biopharma developmentSan matteo foundationResearch centerAstellas pharma incEuropean medicines agencyUniversity of paviaEuropean union eu member statesEuropean unionEuropean commission for treatment of vasomotor symptoms

Vueway® Gadopiclenol Receives Positive CHMP Opinion

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of the macrocyclic, high-relaxivity .

Committee for medicinal products human useEuropean medicines agencyReceives positiveMedicinal productsHuman use

Latest Breaking News On - Receives positive - Page 1 : comparemela.com

Astellas XTANDI™ (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

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

Astellas VEOZATM (fezolinetant) Approved by European Commission for Treatment of Vasomotor Symptoms Associated with Menopause

Vueway® Gadopiclenol Receives Positive CHMP Opinion

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of the macrocyclic, high-relaxivity .Committee for medicinal products human useEuropean medicines agencyReceives positiveMedicinal productsHuman use

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended approval of the macrocyclic, high-relaxivity .

Committee for medicinal products human useEuropean medicines agencyReceives positiveMedicinal productsHuman use