SUTENT® (Sunitinib malate) November 17, 2017April 5, 2020 RR FDA Approvals Renal Cell Carcinoma The FDA on November 16, 2017, approved SUTENT® for the adjuvant treatment of adult patients at high risk of recurrent Renal Cell Carcinoma, following nephrectomy. SUTENT® is a product of Pfizer Inc. Related Posts:Sunitinib Malate for the Treatment of Pancreatic…CABOMETYX® Superior to SUTENT® in Metastatic…Adjuvant Therapy with SUTENT® in High-Risk Renal…FDA Approves Adjuvant Therapy with SUTENT® in…Oncoprescribe Blog Survival benefit with SunitinibEfficacy and safety of regorafenib for advanced…