Overview LAL-BR/2001: Study Treatment to Low Risk ALL Status: Completed Trial end date: 2015-12-01 Target enrollment: Participant gender: Summary The purpose of this study is increase the efficacy of consolidation (C1) after an intensification phase with high dose of methotrexate, applying analysis of minimal residual disease Phase: Phase 4 Details Lead Sponsor: PETHEMA FoundationTreatments: 6-MercaptopurineAsparaginaseCyclophosphamideCytarabineDaunorubicinMercaptopurineMethotrexatePrednisoneVincristine