drugset / Trial / NCT05832320

Optimum Induction Therapy of Low-risk APL

NCT05832320

RandomizedParallel-groupDouble-blindTreatment

Summary

Despite the high cure probability for acute promyelocytic leukemia (APL), a minority of patients will relapse and the risk factors for relapse are unclear. The goal of this clinical trial is to compare the effectiveness and safety of induction of oral all-trans retinoic acid (ATRA) and realgar-indigo naturalis formula (RIF) combined with oral etoposide or daunorubicin as cytoreductive therapies in low-risk APL. The present study was to explored a cytoreduction of an oral etoposide for low-risk APL with dual induction of ATRA and RIF as a high efficacy, low recurrence, and more convenient all-oral regimen.

Timeline

Start
2023-01-01
Primary completion
2024-12-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Daunorubicin Small molecule 20 mg
Comparator Daunorubicin Small molecule 40 mg
Subject Etoposide Small molecule 50 mg Oral