FDA Approves Viral Immunotherapy for Advanced Melanoma
The U.S. Food and Drug Administration granted accelerated approval to Tudriqev, a new viral immunotherapy. The treatment is for advanced melanoma that has not responded to other therapies. This genetically modified oncolytic virus represents a new option for patients.
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WASHINGTON D.C. -- The U.S. Food and Drug Administration (FDA) today approved Tudriqev (vusolimogene oderparepvec-wtpg) for advanced melanoma. This approval specifically targets cases of the skin cancer that have not responded to prior treatments.
Tudriqev is a genetically modified oncolytic viral therapy. It works by infecting and replicating within cancer cells, causing them to burst and release new viruses and tumor-associated antigens, which can then stimulate an immune response against the cancer.
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