Clinical Trial

A Clinical Study to Evaluate the Efficacy and Safety of VG2025 in Intrahepatic Cholangiocarcinoma

Not Yet Recruiting Phase 2
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Summary
VG2025 is a Recombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection. Currently, one phase I dose escalation safety study has been completed in China and the United States respectively, both demonstrating excellent safety profiles with no dose-limiting toxicities (DLTs) observed and no maximum tolerated dose (MTD) identified. Moreover, it has shown preliminary efficacy in treating advanced tumors. Considering the actual clinical needs and the volume of intratumoral administration, a more appropriate recommended phase 2 dose (RP2D) level has been selected for the phase II clinical trial.
Trial Details
NCT Number NCT07522476
Lead Sponsor Virogin Biotech Ltd.
Conditions Intrahepatic Cholangiocarcinoma
Enrollment 30 participants
Start Date 2026-07-01
Primary Completion 2028-01-18 (estimated)
Study Completion 2028-11-13 (estimated)
Updated on ClinicalTrials.gov 2026-04-13