Administration of eribulin mesylate at a dose of 1.4 mg/m2 as an IV bolus infusion over 2-5 minutes on Days 1 and 8 of every cycle, where the duration of each cycle is 21 days. Treatment will continue until disease progression, development of unacceptable toxicity or withdrawal of consent.
Sponsors
Eisai Limited
Phase 3
Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Dacarbazine in Subjects With Soft Tissue Sarcoma
CompletedACTRN12611001074987
Start: 2011-03-22End: 2013-05-28Target: 450Updated: 2026-02-04
Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Treatment of Physician's Choice in Subjects With Advanced Non-Small Cell Lung Cancer
Active, not recruitingACTRN12612000100897
Start: 2011-09-12End: 2012-11-07Target: 540Updated: 2026-02-04