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Ensayos Clínicos

Open-Label Phase 1 Study to Assess the Maximum Tolerated Dose, Pharmacokinetics, and Safety of Ixazomib Administered Intravenously to Pediatric Patients Aged 0 to <18 Years With Relapsed or Refractory Acute Lymphoblastic Leukemia, With or Without Extramedullary Disease, or Lymphoblastic Lymphoma.

Ficha Técnica

Investigador Principal

JOSÉ RAMÓN MOLINA HURTADO

Promotor

TAKEDA FARMACEUTICA ESPAÑA,S.A.U

ESTADO

VIAIBILIDAD

DEPARTAMENTO

Hematología y Hemoterapia

Número protocolo: Viabilidad 26

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Fecha Fin: