Overview

A Study of XY0206 Tablets in Patients With Relapsed / Refractory Acute Myeloid Leukemia

Status:
Recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
Summary
1. To evaluate the safety and tolerability of xy0206 as single drug in the treatment of relapsed / refractory AML; 2. Evaluate the dose limited toxicity (DLT) and maximum tolerable dose (MTD) of xy0206 as single drug in the treatment of relapsed / refractory AML subjects. 3. To evaluate the pharmacokinetic (PK), pharmacokinetic (PD) characteristics and PK / PD correlation of xy0206 as single drug treatment in relapsed / refractory AML subjects; 4. To evaluate the primary efficacy of xy0206 as single drug in the treatment of relapsed / refractory AML patients; 5. To evaluate biomarkers of xy0206 as single drug treatment for relapsed / refractory AML subjects.
Phase:
Phase 1
Details
Lead Sponsor:
Shijiazhuang Yiling Pharmaceutical Co. Ltd
Collaborator:
Proswell Medical Corporation