BeiGene/Amgen’s DLL3/CD3 bispecific antibody is approved for domestic market launch
July 21, 2025
Source: drugdu
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The CDE official website shows that BeiGene and Amgen's application for taratumumab injection has been accepted for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC) who have failed at least 2 lines of treatment (including platinum-containing chemotherapy). This indication has been included in the priority review. Globally, only one DLL3/CD3 dual antibody, taratumumab, has been approved for marketing. In addition, there are 4 other products that have entered the clinical stage, with the highest progress being clinical phase II. In terms of clinical progress, taratumumab has a first-mover advantage.
https://finance.sina.com.cn/roll/2025-07-17/doc-infftyiu0311325.shtml
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