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Clinical Trial Summary

To compare the efficacy and safty of ABC-14 regimen with the traditional "3+7" regimen or AB-14 regimen in the treatment of newly diagnosed acute myeloid leukaemia


Clinical Trial Description

Acute myeloid leukemia (AML) is a clonal malignant blood disease with genetic heterogeneity and originated from hematopoietic stem progenitor cells.In the past 50 years, the "3+7" induction regimen represented by cytotoxic drugs (including anthracyclines/anthraquinones combined with cytarabine) has remained the standard induction regimen for newly diagnosed AML patients with intensive chemotherapy. In AML patients <60 years old, the "3+7" regimen induces a complete response rate of 60% to 80%, but the treatment-related mortality is as high as 13%, and more than half of the patients face the threat of relapse, and the 5-year overall survival rate is about 35% to 40%. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06451861
Study type Interventional
Source Guangdong Provincial People's Hospital
Contact Jianyu Weng
Phone 020-83827812
Email wengjianyu@gdph.org.cn
Status Not yet recruiting
Phase Phase 2
Start date May 31, 2024
Completion date June 30, 2027

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