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Giants of Cancer Care® Announces the 12th Annual Class of Inductees

The 15 inductees have been selected by their peers for their remarkable achievements in oncology research and clinical practice.

United statesUniversity of chicagoAdler planetariumRafael fonsecaCarola aghajanianFabrice andrMike hennessy jrGuillermo garcia maneroSolangeg petersRalphr weichselbaumEdwards kimMichaelj hennessyEthanm baschLynnm schuchterJosepha sparanoJulia paradizova

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults -March 28, 2024 at 06:46 am EDT

Decision marks the first approval in Europe for an anti-PD-1/L1 therapy in resectable NSCLC based on positive overall survival results and represents the sixth approval for KEYTRUDA in lung cancer in.

United statesSolange petersExchange commissionMerck research laboratoriesStatement of merck co incCentre hospitalier universitaire vaudoisCommittee for medicinal products humanMerck co incEuropean commissionMedicinal productsHuman useMarjorie greenMerck researchAmerican joint committeeCancer staging manualSelected important safety

Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC

Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC
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United statesJulie cunninghamDamini chokshiSolange petersPeter dannenbaumMerck research laboratoriesStatement of merck co incCentre hospitalier universitaire vaudoisEuropean commissionExchange commissionCommittee for medicinal products humanMerck co incMedicinal productsHuman useMarjorie greenMerck research

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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United statesSolange petersExchange commissionEuropean commissionEuropean commission approves merckProduct serviceMerck co incCommittee for medicinal products humanStatement of merck co incCentre hospitalier universitaire vaudoisMerck research laboratoriesNeoadjuvant treatmentThen continuedAdjuvant treatmentResectable non small cell lung cancerHigh risk

Perioperative Pembrolizumab Wins Approval in Europe for Resectable NSCLC at High Risk of Recurrence

The European Commission has approved neoadjuvant pembrolizumab plus chemotherapy, followed by adjuvant pembrolizumab, for high-risk, resectable NSCLC.

United statesMerck keytrudaSolange petersAmerican joint committee on cancer staging manualCentre hospitalier universitaire vaudoisEuropean commissionAmerican joint committeeCancer stagingImmuno oncologyLung cancerGlobal oncologyThe european commissionNeoadjuvant pembrolizumab plus chemotherapyOllowed by adjuvant pembrolizumabHigh riskResectable nsclc