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Study identifier: NCT06237192 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

MRD-associated Non-intensive But Non-interruptive Treatment of Ph-negative Acute Lymphoblastic Leukemia Adult Patients

Condition: Precursor Cell Lymphoblastic Leukemia-Lymphoma  ·  Sponsor: National Research Center for Hematology, Russia

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersNo

About this study

Non-intensive But Non-interruptive Treatment based on previously study RALL-2016 of Adult Ph-negative Acute Lymphoblastic Leukemia: No high-dose methotrexate (MTX) and high-dose cytarabine (ARA-C) consolidation blocks, L-asparaginaseis scheduled for 1 year of treatment, 21 intrathecal injections through the whole treament, T-ALL patients in complete remission (CR) with MRD-positive status after 2nd induction receive consolidation 1-3 with venetoclax (56 days), and B-ALL patients in complete remission (CR) with MRD-positive status after 2nd induction receive 1 consolidation with blinatumomab. After that consolidation bone samples are collected and tested for MRD and patients will continue therapy by protocol without HSCT if MRD-negative (by flow cytometry by aberrant immunophenotype in a centralized lab) status was achieved.

This description comes directly from the study's public registry record.

Talk to the study team

Olga Aleshina, MD, PhD  ·  +79629745058  ·  dr.gavrilina@mail.ru

Always discuss trial participation with your own doctor first.

Locations (1)

Olga AleshinaMoscow, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06237192