At a glance
ClinicalIndex Comparison Record- ✓Age ≥36 months and <22 years
- ✓Pathologically proven malignant cerebellar brain tumor (medulloblastoma, glioblastoma, astrocytoma, PNET, ependymoma, atypical teratoid/rhabdoid, germ cell, or other high-grade malignant tumor)
- ✓Progressive or recurrent despite standard care
- ✓Tumor ≥1.0 cm to ≤3.0 cm in diameter and surgically accessible
- ✕Diffuse, widespread abnormal tumor pattern involving 3 or more brain lobes
- ✕Acute infection, granulocytopenia, or medical condition precluding surgery
- ✕Pregnant or lactating females
- ✕Encephalitis or CNS infection <3 months prior, or ongoing treatment for encephalitis, CNS infection, or multiple sclerosis
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Phase 1 Trial of Engineered HSV G207 in Children With Recurrent or Refractory Cerebellar Brain Tumors
In Brief
A Phase 1 clinical trial evaluating G207 for Neoplasms, Brain and 32 related conditions. Currently recruiting, targeting 24 participants across 3 sites.
Detailed Summary
This study is a clinical trial to determine the safety of inoculating G207 (an experimental virus therapy) into a recurrent or refractory cerebellar brain tumor. The safety of combining G207 with a single low dose of radiation, designed to enhance virus replication, tumor cell killing, and an anti-tumor immune response, will also be tested. Funding Source- FDA OOPD
Study Details
Timeline
Interventions
Single dose of G207 infused through catheters into region(s) of tumor. If G207 is safe in the first cohort of patients, subsequent patients will receive a single dose of G207 infused through catheters into region(s) of tumor followed by a 5 Gy dose of radiation to the tumor (which includes progressive leptomeningeal disease or any site of gross tumor progressing in the brain parenchyma) within 24 hours of virus inoculation.