European Commission approves Tevimbra as neo-adjuvant/adjuvant NSCLC treatment

BeiGene

27 August 2025 - Final analysis of RATIONALE-315 demonstrates clear overall survival benefit in peri-operative setting in resectable non-small cell lung cancer.

BeOne Medicines today announced that the European Commission has approved Tevimbra (tislelizumab), in combination with platinum-containing chemotherapy as neo-adjuvant treatment followed by Tevimbra monotherapy as adjuvant treatment, for adult patients with resectable non-small cell lung cancer at high risk of recurrence.

Read BeOne Medicines press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Registration