BeiGene has won the first FDA approval for its PD-1 inhibitor, marking a hard-earned milestone after a winding regulatory journey that began two and a half years ago.
Tevimbra, the brand name for the antibody also known as tislelizumab, will be available in the US in the second half of 2024, BeiGene said in a press release. It is cleared to treat metastatic esophageal squamous cell carcinoma (ESCC) after prior chemotherapy.
Unlock this article instantly by becoming a free subscriber.
You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.