BeiGene receives FDA approval for Tevimbra for the treatment of advanced or metastatic oesophageal squamous cell carcinoma after prior chemotherapy

BeiGene

14 March 2024 - Results from the global, Phase 3 RATIONALE 302 trial showed Tevimbra prolonged the survival of patients who received prior systemic treatment compared to chemotherapy.

BeiGene today announced that the US FDA has approved Tevimba (tislelizumab-jsgr) as monotherapy for the treatment of adult patients with unresectable or metastatic esophageal squamous cell carcinoma after prior systemic chemotherapy that did not include a PD-(L)1 inhibitor.

Read BeiGene press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US