FDA Approves Merck's KEYTRUDA To Treat High-Risk Early-Stage Triple-Negative Breast Cancer
nasdaq.com
FDA Approves Merck's KEYTRUDA To Treat High-Risk Early-Stage Triple-Negative Breast Cancer
(RTTNews) - The U.S. Food and Drug Administration has approved Merck & Co., Inc.'s (MRK) anti-PD-1 therapy, KEYTRUDA, for the treatment of patients with high-risk early-stage triple-negative breast cancer or TNBC in combination with chemotherapy as neoadjuvant treatment and then
Jul 27, 2021
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Important updates on locally advanced head and neck squamous cell carcinoma (LA-HNSCC) were presented this year at the #ESMO20 Virtual Congress. In this video, Jean Bourhis reports on key results from the GORTEC 2015-01 “PembroRad” trial testing pembrolizumab vs cetuximab, concomitant with radiotherapy in LA-HNSCC. For more ESMO videos ▶️ http://ow.ly/BeEW50CPkTi #oncology #educationforLIFE | ESMO - European Society for Medical Oncology
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Important updates on locally advanced head and neck squamous cell carcinoma (LA-HNSCC) were presented this year at the #ESMO20 Virtual Congress. In this video, Jean Bourhis reports on key results from the GORTEC 2015-01 “PembroRad” trial testing pembrolizumab vs cetuximab, concomitant with radiotherapy in LA-HNSCC. For more ESMO videos ▶️ http://ow.ly/BeEW50CPkTi #oncology #educationforLIFE | ESMO - European Society for Medical Oncology
FacebookESMO - European Society for
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NICE recommends pembrolizumab for 1,600 more people with breast cancer - Cancer Research UK - Cancer News
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