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Clinical Trials in China / NCT07589257
Recruiting Phase 2

A Study of VRT106 in Combination With Radiotherapy in Adult Patients With Diffuse Midline Glioma / Diffuse Intrinsic Pontine Glioma

NCT07589257 · tracked via the Priya Life Science China tracker
Sponsor
Guangzhou Virotech Pharmaceutical Co., Ltd.
Phase
Phase 2
Started
2026-05-07
Last updated
2026-05-15

Condition(s) studied

Diffuse Midline Glioma, H3 K27M-MutantDiffuse Intrinsic Pontine Glioma

Investigational drug(s) / intervention(s)

VRT106 for injection

VRT106 for injection: VRT106, iv

Study summary

To Evaluate the Preliminary Efficacy and Safety/Tolerability of VRT106 Combined with Radiotherapy in Adult Patients with DMG/DIPG

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Voluntary signing of the Informed Consent Form (ICF), indicating understanding of the study and willingness and ability to comply with all study procedures. * Male or female adults aged 18 to 75 years at the time of signing the ICF. * Histologically or cytologically confirmed H3 K27-altered diffuse midline glioma (DMG), or a diagnosis of DIPG based on brain contrast-enhanced MRI: tumor originating in the pons, occupying \>50% of the pons volume, with diffuse brainstem enlargement. * Karnofsky Performance Status (KPS) score ≥ 60. * Expected survival time ≥ 3 months. Exclusion Criteria: * Individuals with extracranial metastases. * Presence of spinal cord tumors or evidence of leptomeningeal disease dissemination. * Active hemorrhage detected on cranial MRI scan prior to enrollment. * Inability to undergo cranial MRI scanning (e.g., due to contraindications or incompatible implants). * Prior receipt of oncolytic virus therapy or other gene therapy agents.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sun Yat-sen University Cancer Center Guangzhou Guangdong Recruiting

More Guangzhou Virotech Pharmaceutical Co., Ltd. trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07589257 on ClinicalTrials.gov ↗ ← All trials in China