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TIL + Pembrolizumab

Advanced Front-line Melanoma

Phase 3ActiveTILVANCE-301

Key Facts

Indication
Advanced Front-line Melanoma
Phase
Phase 3
Status
Active
Company

About Iovance Biotherapeutics

Iovance Biotherapeutics' mission is to be the global leader in developing and delivering TIL therapy for cancer. Its landmark achievement is the FDA accelerated approval of Amtagvi™ (lifileucel) in February 2024, the first-ever approved TIL therapy, validating its core platform. The company's strategy is to commercialize Amtagvi in melanoma, expand its label into earlier lines of therapy and new tumor types, and advance next-generation genetically modified TIL therapies through its integrated manufacturing facility, the Iovance Cell Therapy Center (iCTC).

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About Iovance Biotherapeutics

Iovance Biotherapeutics' mission is to be the global leader in developing and delivering TIL therapy for cancer. Its landmark achievement is the FDA accelerated approval of Amtagvi™ (lifileucel) in February 2024, the first-ever approved TIL therapy, validating its core platform. The company's strategy is to commercialize Amtagvi in melanoma, expand its label into earlier lines of therapy and new tumor types, and advance next-generation genetically modified TIL therapies through its integrated manufacturing facility, the Iovance Cell Therapy Center (iCTC).

View full company profile

Therapeutic Areas