BeOne gains first-line EU nod for checkpoint blocker
The European medicines regulator has approved a combo therapy starring PD-1 inhibitor Tevimbra (tislelizumab), from cancer firm BeOne Medicines, formerly BeiGene (HKEX: 06160).
The nod covers use of the biologic, together with chemotherapy, for the first-line treatment of certain advanced throat and stomach cancers. The therapy is backed by positive results from two global Phase III trials: RATIONALE-306 and RATIONALE-305.
Commenting on the decision, Florian Lordick of the University Cancer Center Leipzig said: "The compelling data...underscore the unique clinical profile of tislelizumab, offering new hope where it’s needed most."
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