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Johnson & Johnson's amivantamab showed a 45% response rate in hard-to-treat head and neck cancer, with rapid, lasting tumor shrinkage.
Johnson & Johnson reported that subcutaneous amivantamab achieved a 45% overall response rate in patients with HPV-unrelated recurrent or metastatic head and neck cancer who had failed prior treatments, with responses lasting a median of 7.2 months and occurring rapidly.
The drug, which targets EGFR and MET, showed tumor shrinkage in 82% of patients after 8.3 months of follow-up.
Administered via a five-minute injection, it offers a convenient alternative to IV therapy.
Results from the Phase 1b/2 OrigAMI-4 study were presented at ESMO 2025, highlighting potential for this bispecific antibody as a new option for a group with limited treatments and poor prognosis.
El amivantamab de Johnson & Johnson mostró una tasa de respuesta del 45% en cáncer de cabeza y cuello difícil de tratar, con una reducción rápida y duradera del tumor.