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Mabwell Reports Promising Clinical Results for Nectin-4 ADC 9MW2821

Mabwell Reports Promising Clinical Results for Nectin-4 ADC 9MW2821

At the 2026 ESMO Gynaecological Cancers Congress in Copenhagen, Mabwell presented new clinical data for 9MW2821, a Nectin-4-targeting antibody-drug conjugate. The study highlighted the drug’s efficacy in treating advanced cervical cancer, showing notable survival benefits for patients previously treated with immunotherapy.

Prof. Yang Huijuan of Fudan University Shanghai Cancer Center detailed the findings from a Phase I/II trial involving 55 patients with recurrent or metastatic cervical cancer. Among those evaluable for efficacy, the confirmed objective response rate reached 32.08%, with a disease control rate of 81.13%. Patients previously treated with immune checkpoint inhibitors saw a median progression-free survival of 4.0 months, while median overall survival had not yet been reached at the time of the data cut-off.

A separate study evaluated 9MW2821 in combination with the PD-1 inhibitor toripalimab. Preliminary data from 19 patients showed an objective response rate of 76.9%, climbing to 80% among treatment-naïve patients. The combination therapy demonstrated a manageable safety profile, with most adverse events categorized as Grade 1 or 2, suggesting a potential path forward for first-line treatment protocols in cervical cancer care.

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