An Expanded Access Program for VO (RP1) in Combination With Nivolumab in Patients With Advanced Melanoma

NCT06590480 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2025-12-18

No results posted yet for this study

Summary

The purpose of this EAP is to provide expanded access (i.e., before marketing authorization) to vusolimogene oderparepvec (VO; herein referred to as VO) plus standard-of-care (SOC), nivolumab, for eligible patients diagnosed with advanced melanoma, who, in their treating physician's opinion, could benefit from this treatment.

Conditions

Interventions

BIOLOGICAL

RP1

Genetically modified Herpes Simplex Type 1 Virus

BIOLOGICAL

Nivolumab

Anti-PD-1 Monoclonal Antibody

Sponsors & Collaborators

  • Replimune Inc.

    lead INDUSTRY

Principal Investigators

  • Tom Hash, MD · Replimune Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06590480 on ClinicalTrials.gov