drugset / Trial / NCT05477849

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Biologic Effect of VG2025 in Patients with Solid Tumors

NCT05477849

Phase 1 Recruiting 30 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
2022-08-23
Primary completion
2025-10-31
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject VG2025 Unknown

Indications