HALAVEN® (Eribulin) August 1, 2016April 5, 2020 RR FDA Approvals Soft Tissue Sarcomas - Trunk and Extremities The FDA on January 28, 2016 approved HALAVEN® for the treatment of patients with unresectable or metastatic Liposarcoma who have received a prior Anthracycline-containing regimen. HALAVEN® is a product of Eisai Co., Ltd. Related Posts:FDA Approves HALAVEN® for Advanced LiposarcomaOncoprescribe Blog Eribulin improves survival in…A phase III study (EMBRACE) of eribulin mesylate…