Vusolimogene oderparepvec

DB23008ApprovedInvestigationalGene Therapies

Vusolimogene oderparepvec is a genetically modified HSV-1 oncolytic viral immunotherapy used intratumorally with nivolumab for unresectable advanced cutaneous melanoma refractory to anti-PD-1 therapy, replicating selectively in tumor cells and expressing GALV-GP-R– and GM-CSF to drive anti-tumor immunity. The virus is engineered to express a fusogenic glycoprotein derived from gibbon ape leukemia virus (GALV-GP-R–) and human granulocyte-macrophage colony-stimulating factor (GM-CSF), and has its HSV-1 neurovirulence factor ICP34.5 and antigen-presentation inhibitor ICP47 genes deleted.

Primary indication
Vusolimogene oderparepvec-wtpg is indicated in combination with nivolumab for the treatment of adult patients with unresectable advanced cutaneous melanoma who experienced disease progression with a programmed death receptor-1 (PD-1)-blocking antibody-based regimen.Curator reviewed · 1 structured indication
First approval
United States, 2026
Brand names
  • Tudriqev

Resolves to

Clinical / RWD

What you can answer from here — as of September 14, 2026

6Clinical trialsPhase, status and sponsor resolved per trial
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1Structured indicationCondition, population, route and combination as fields, not prose
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2Marketed productsAcross 1 country and 1 labeller
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3+ReferencesStructured and connected to the statements they support
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Which other approved drugs treat the same conditions as Vusolimogene oderparepvec, and which companies have late-stage candidates in those indications?

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