The purpose of this study is to evaluate the safety and tolerability of an investigational drug called LYT 200 in two types of blood and bone marrow cancer: acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). The study focuses on individuals who have had at least one line of therapy for AML or MDS and whose cancer has relapsed or was refractory (resistant) to treatment. Researchers will also examine how LYT-200 is changed by and removed from the body, as well as evaluate its preliminary effectiveness and recommended dose. LYT-200 is intended to inhibit (hinder) galectin 9, which is a protein that suppresses immune function and disables immune-mediated attack on the cancer cells. Participants will receive 1 of 5 different doses of LYT-200 in this study.
What is the full name of this clinical trial?
LYT-200-2022-02: A Phase 1 Open-label, Multi-center Study of the Safety, Pharmacokinetics , and Anti-tumor Activity of LYT- 200 in Patients with Relapsed/refractory Acute Myeloid Leukemia , or with Relapsed/refractory, High-risk Myelodysplastic Syndrome