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Phase I study of the novel, fully synthetic epothilone sagopilone (ZK-EPO) in patients with solid tumors
Annals of Oncology, 11/04/09
Schmid P et al. – Sagopilone (ZK–EPO) is a fully synthetic microtubule–stabilizing agent that has demonstrated high antitumor activity in preclinical models. This first–in–human phase I study aimed to determine the maximum tolerated dose (MTD) and dose–limiting toxic effects (DLTs) of 3–weekly sagopilone treatment. These data demonstrate that sagopilone therapy is feasible and well tolerated. The recommended dose for phase II studies is 16.53 mg/m^2, once every 3 weeks.
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