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Updated: Mar 24, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
First oncolytic virus approved for melanoma immunotherapy
Jonathan Pol1, Guido Kroemer2, Lorenzo Galluzzi3
1INSERM, U1138, Paris, France; Université Paris Descartes/Paris V, Sorbonne Paris Cité, Paris, France; Université Pierre et Marie Curie/Paris VI, Paris, France; Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers, Paris, France; Gustave Roussy Cancer Campus, Villejuif, France.
The US FDA approved talimogene laherparepvec (T-VEC) in 2015. This oncolytic virus therapy is for melanoma patients with non-resectable lesions.
Area of Science:
- Oncolytic virotherapy
- Cancer immunology
- Melanoma treatment
Background:
- Talimogene laherparepvec (T-VEC) is an oncolytic virus therapy.
- It is designed to treat melanoma patients with unresectable lesions.
Purpose of the Study:
- To report the US FDA approval of talimogene laherparepvec (T-VEC).
- To highlight T-VEC as the first oncolytic virus approved for cancer therapy in the US.
Main Methods:
- The US Food and Drug Administration (FDA) reviewed talimogene laherparepvec (T-VEC).
- Approval was granted for injectable, non-resectable skin and lymph node lesions in melanoma patients.
Main Results:
- Talimogene laherparepvec (T-VEC) received official FDA approval on October 27th, 2015.
- T-VEC, commercialized as Imlygic® by Amgen, Inc., is the first oncolytic virus approved in the US.
Conclusions:
- The approval of T-VEC marks a significant advancement in oncolytic virus therapy for cancer.
- This milestone provides a new therapeutic option for melanoma patients with specific lesion types.
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