Last reviewed · How we verify

NCT06590480: RPL-EAP-001

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

NO LONGER AVAILABLE Last updated 18 December 2025
What this trial tests

trial testing RP1 in Advanced Melanoma. No longer available.

Quick facts

Lead sponsorReplimune, Inc.
StatusNO LONGER AVAILABLE
Study typeEXPANDED_ACCESS

Drugs / interventions tested

Conditions studied

Sponsor

Replimune, Inc.

Who can join

18 and older, any sex, with Advanced Melanoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Oncolytic HSV and cancer drug interactions: Current clinical status and future directions.
    Vázquez-Arreguín K, Rivera-Caraballo KA, Ventarapragada D, Chiocca EA, et al · · 2025 · cited 6× · PMID 40702727 · DOI 10.1016/j.ymthe.2025.07.034

Verify or expand the search:

Other recruiting trials for Advanced Melanoma

Currently open trials in the same condition.

Other Replimune, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06590480.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing