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Lynparza plus abiraterone reduced risk of disease progression by 34% vs standard-of-care in 1st-line metastatic castration-resistant prostate cancer

Lynparza plus abiraterone reduced risk of disease progression by 34% vs standard-of-care in 1st-line metastatic castration-resistant prostate cancer
astrazeneca.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from astrazeneca.com Daily Mail and Mail on Sunday newspapers.

United statesUnited kingdomFred saadRoy baynesSusan galbraithAmerican society of clinical oncologyInternational journal of clinical practiceData monitoring committeeUniversity of montreal hospital centerMerck co incCompany on twitter astrazenecaResearch laboratoriesInvestor relations teamHead of global clinical developmentClinical oncologyGenitourinary cancers

Lynparza plus abiraterone reduced risk of disease progression by 34% vs standard-of-care in 1st-line metastatic

Lynparza plus abiraterone reduced risk of disease progression by 34% vs standard-of-care in 1st-line metastatic
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United statesFred saadRoy baynesSusan galbraithResearch laboratoriesAmerican society of clinical oncologyHead of global clinical developmentUniversity of montreal hospital centerClinical oncologyGenitourinary cancersGenitourinary oncologyMontreal hospital centerExecutive vice presidentSenior vice presidentGlobal clinical developmentChief medical officer

Pivotal Phase 3 Data for KEYTRUDA (pembrolizumab) in High-Risk Early-Stage Triple-Negative Breast Cancer (TNBC) Published in the New England Journal of Medicine

09.02.2022 - Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced the publication of results from the Phase 3 KEYNOTE-522 trial in the Feb. 10, 2022 edition of the New England Journal of Medicine. Results showed that neoadjuvant .

United statesCity ofUnited kingdomPeter schmidRoy baynesMerck research laboratoriesCentre for experimental cancer medicineStatement of merck co incMerck co incExchange commissionBarts cancer instituteExperimental cancer medicineMerck researchNew england journalAdditional data fromCombined positive score

FDA Rejects Gefapixant NDA for Chronic Cough

The FDA has issued a CRL regarding the NDA for gefapixant for the treatment of adults with refractory or unexplained chronic cough.

Roy baynesMerck research laboratoriesDrug administrationComplete response letterNew drug applicationMerck research

Merck Provides U S and Japan Regulatory Update for Gefapixant

Merck Provides U.S. and Japan Regulatory Update for Gefapixant - read this article along with other careers information, tips and advice on BioSpace

United statesRoy baynesMerck research laboratoriesDrug administrationMerck coStatement of merck co incExchange commissionMerck co incJapan ministry of healthComplete response letterNew drug applicationMerck researchJapan ministryLooking statementSecurities litigation reform actErck provides us and japan regulatory update for gefapixant