drugset / Trial / NCT07682870

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of VG2025 Intravenous Injection in Subjects With Advanced Solid Tumors

NCT07682870

Phase 1/2 Not yet recruiting 42 enrolled Virogin Biotech Ltd.
NaSingle-groupOpen-labelTreatment

Summary

VG2025 is a Recombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection. This Phase I study will be conducted in herpes simplex virus (HSV) -seropositive subjects with advanced malignant solid tumors that are refractory to conventional therapies. This is an open label study to determine the safety and tolerability of VG2025, and recommended dose of VG2025 for Phase II trials.

Timeline

Start
2026-09-04
Primary completion
2028-12-02
Completion
2029-09-03

Drugs

EvaluationDrugModalityDoseRoute
Subject VG2025 Unknown Intravenous

Indications