FDA granted regular approval to pembrolizumab (KEYTRUDA, Merck and Co., Inc.) for patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. May 18, 2017. More Information: https://www.fda.gov/Drugs/
viernes, 19 de mayo de 2017
Approved Drugs > Pembrolizumab (Keytruda): Advanced or Metastatic Urothelial Carcinoma
Approved Drugs > Pembrolizumab (Keytruda): Advanced or Metastatic Urothelial Carcinoma
FDA granted regular approval to pembrolizumab (KEYTRUDA, Merck and Co., Inc.) for patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. May 18, 2017. More Information: https://www.fda.gov/Drugs/ InformationOnDrugs/ ApprovedDrugs/ucm559300.htm
FDA granted regular approval to pembrolizumab (KEYTRUDA, Merck and Co., Inc.) for patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. May 18, 2017. More Information: https://www.fda.gov/Drugs/
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