Myelodysplastic Syndrome Clinical Trial
Official title:
Phase I Clinical Trial of SyB L-1101 in Patients With Myelodysplastic Syndrome
The purpose of this study is to investigate tolerability when SyB L-1101 is administered intravenously in patients with recurrent/relapsed or refractory myelodysplastic syndrome, to determine the dose-limiting toxicity and maximum tolerated dose, and to estimate the recommended dose for phase II studies. Pharmacokinetics and antitumor effects will also be investigated.
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