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Recurrent Medulloblastoma clinical trials

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NCT ID: NCT03299309 Not yet recruiting - Malignant Glioma Clinical Trials

PEP-CMV in Recurrent MEdulloblastoma/Malignant Glioma

PRiME
Start date: December 2017
Phase: Phase 1
Study type: Interventional

The primary goal of this prospective clinical trial is to evaluate the safety of PEP-CMV in patients with recurrent medulloblastoma and malignant glioma. Patients with histologically-proven medulloblastoma or malignant glioma who had received definitive chemo-radiotherapy and subsequently had tumor recurrence/progression may be enrolled any time after recurrence/progression regardless of prior adjuvant therapy. PEP-CMV is a vaccine mixture of 2 peptides comprised in two components (referred to as Component A and Component B). Component A is a synthetic long peptide (SLP) of 26 amino acid residues from human pp65. Component B consists of a neutralizing antibody epitope from human CMV glycoprotein B (gB) conjugated to KLH.

NCT ID: NCT03233204 Recruiting - Malignant Glioma Clinical Trials

Pediatric MATCH: Olaparib in Treating Patients With Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphoma, or Histiocytic Disorders With Defects in DNA Damage Repair Genes

Start date: July 24, 2017
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well olaparib works in treating patients with solid tumors, non-Hodgkin lymphoma, or histiocytic disorders with defects in deoxyribonucleic acid (DNA) damage repair genes that have spread to other places in the body and have come back or do not respond to treatment. Olaparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT03213665 Recruiting - Malignant Glioma Clinical Trials

Pediatric MATCH: Tazemetostat in Treating Patients With Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphoma, or Histiocytic Disorders With EZH2, SMARCB1, or SMARCA4 Gene Mutations

Start date: July 24, 2017
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well tazemetostat works in treating patients with solid tumors, non-hodgkin lymphoma, or histiocytic disorders that have spread to other places in the body and have come back or do not respond to treatment and have EZH2, SMARCB1, or SMARCA4 gene mutations. Tazemetostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.