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FDA approves BeiGene's Tevimbra with chemotherapy for advanced gastric cancers expressing PD-L1.
The FDA has approved BeiGene's Tevimbra drug in combination with chemotherapy for the first-line treatment of advanced HER2-negative gastric or gastroesophageal junction cancers that express PD-L1.
This approval follows a successful Phase 3 trial showing improved overall survival compared to chemotherapy alone.
Tevimbra is now approved in the U.S. for two types of cancer treatments.
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La FDA aprueba Tevimbra de BeiGene con quimioterapia para cánceres gástricos avanzados que expresan PD-L1.