drugset / Trial / NCT03125876

A Phase Ib Study of CT053PTSA in Relapsed / Refractory Acute Myeloid Leukemia (AML)

NCT03125876

Phase 1 Terminated 12 enrolled Sunshine Lake Pharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of CT053PTSA in Relapsed/refractory AML patients with FLT3 gene mutation.

Timeline

Start
2017-11-13
Primary completion
2019-08-19
Completion
2019-08-19

Drugs

EvaluationDrugModalityDoseRoute
Subject CT053PTSA Unknown 60 mg Oral
Subject CT053PTSA Unknown 80 mg Oral
Subject CT053PTSA Unknown 100 mg Oral