Open-Label Study to Evaluate the Safety, Tolerability and Efficacy of the Oncolytic HSV1 MVR-C5252

PHASE1RecruitingINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

June 11, 2024

Primary Completion Date

December 1, 2026

Study Completion Date

December 1, 2027

Conditions
Recurrent High Grade Glioma
Interventions
BIOLOGICAL

MVR-C5252

MVR-C5252 is a genetically modified next generation oncolytic herpes simplex virus 1 (oHSV1) with an active domain of human IL-12 and Fab fragment of anti-PD-1 antibody. This is a Phase 1 open label study designed to determine the safety and tolerability of MVR-C5252. The dose-escalation portion of the study will be conducted in 4 stages to evaluate the safety of infusion and determination of the MTD/RP2D followed by efficacy assessment.

Trial Locations (1)

27750

RECRUITING

Duke University, Durham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Duke University

OTHER