CI

At a glance

ClinicalIndex Comparison Record
Phase 1Recruiting· 24 target
Drug / intervention
G207biological
Likely dose
Not stated in record
Key inclusion· 8
  • 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
Key exclusion· 11
  • 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.

Search/NCT03911388
NCT03911388Phase 1RecruitingOn Track
Long Recruiting

Phase 1 Trial of Engineered HSV G207 in Children With Recurrent or Refractory Cerebellar Brain Tumors

M.D. Anderson Cancer Center·interventional·Posted Apr 11, 2019·Updated May 15, 2026

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

Phase 1Recruiting
20202021202220232024202520262027
First PostedApr 11, 2019
Enrollment StartSep 12, 2019
Primary CompletionSep 1, 2026
Study CompletionSep 1, 2027
TodayJul 2, 2026
Enrollment to primary: 7.0 yearsPosted 7.2 years agoPrimary completion in 2 months

Interventions

G207biological

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.