CI

At a glance

ClinicalIndex Comparison Record
Phase 3Unknown· 82 target
Drug / intervention
Tyrosine kinase inhibitor (TKIs)drug
Likely dose
Tyrosine kinase inhibitor (TKIs) 200mgfrom record
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Search/NCT03624530
NCT03624530Phase 3Unknown

Effect of Prophylactic Tyrosine Kinase Inhibitor Therapy Post-transplants on Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia Undergoing Allo-HSCT With Minimal Residual Disease Positive Pre-transplants

Nanfang Hospital, Southern Medical University·interventional·Posted Aug 10, 2018·Updated Aug 10, 2018

In Brief

A Phase 3 clinical trial evaluating Tyrosine kinase inhibitor (TKIs) for Philadelphia Chromosome Positive Acute Lymphocytic Leukemia and 3 related conditions. Targeting 82 participants across 1 site.

Detailed Summary

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) in early first complete remission improves the long-term outcomes for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). Relapse remains a major cause of treatment failure even after allo-HSCT. The prevention of relapse is essential for improving the outcome of Ph+ ALL. Our previous clinical trial (ID: NCT01883219) demonstrated that pre-emptive tyrosine kinase inhibitor (TKIs) administration based on minimal residual disease (MRD) and BCR-ABL mutation after allo-HSCT might reduce the incidence of relapses and improve survival for patients with Ph+ ALL. Moreover, our result suggested that Ph+ ALL with MRD positive pre-transplants had the higher rate of molecular biology relapse. In this study, we will evaluate the safety and efficacy of prophylactic TKI therapy post-transplants on Ph+ ALL undergoing allo-HSCT with MRD positive pre-transplants.

Study Details

Timeline

Phase 3UnknownOverdue
20192020202120222023202420252026
First PostedAug 10, 2018
Enrollment StartAug 1, 2018
Primary CompletionJul 1, 2021
Study CompletionJul 1, 2022
TodayJul 1, 2026
Enrollment to primary: 2.9 yearsPosted 7.9 years ago

Interventions

Tyrosine kinase inhibitor (TKIs)drug

TKI was selected according to the mutation results of ABL kinase region. Imatinib was initiated at a dose of 200mg/d, dasatinib at a dose of 50mg/d, and ponatinib at a dose of 30mg/d. Then increase the dosage of TKI gradually and increase to therapeutic dose within one month. The duration of TKI was 180 days.