The US Food and Drug Administration (FDA) has approved ramucirumab (Cyramza) to treat patients with advanced gastric cancer or gastroesophageal junction adenocarcinoma. It is a fully human monoclonal antibody of the IgG1 class, directed against the vascular endothelial growth factor receptor 2 (VEGFR2). Ramucirumab is intended for patients with unresectable or metastatic disease after treatment with a fluoropyrimidine- or platinum-containing therapy. Read more
here.
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