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Sanofi and its partner Regeneron recently announced the evaluation of anti-PD-1 therapy Libtayo (cemiplimab) combined with platinum-containing dual-action chemotherapy for the treatment of stage 3 EMPOWER-Lung 3 in patients with advanced non-small cell lung cancer (NSCLC) The positive result of the test
The trial enrolled patients with locally advanced or metastatic disease, tumors with squamous or non-squamous histology, and all PD-L1 expression levels, and compared Libtayo+ chemotherapy with chemotherapy alone
——Overall survival (OS): Compared with the chemotherapy group, the Libtayo+ chemotherapy group has significantly longer OS (median OS: 22 months vs 13 months) and a 29% reduction in the risk of death (HR=0.
——Progress-free survival (PFS): Compared with the chemotherapy group, the PFS of the Libtayo+ chemotherapy group was significantly prolonged (median PFS: 8 months vs.
——Remission: The objective response rate (ORR) in the Libtayo+ chemotherapy group was 43%, and the median duration of response (DOR) was 16 months; the ORR in the chemotherapy group was 23% and the median DOR was 7 months
-Patient-reported results: Good results reported by patients were observed in this trial
——Safety: No new Libtayo safety signal was found in this test
The data from the Phase 3 EMPOWER-Lung 3 trial will serve as the basis for the submission of regulatory application documents in the United States and the European Union
Lung cancer is the leading cause of cancer deaths worldwide
Libtayo is an anti-PD-(L)1 inhibitor, which aims to use the body's own immune system to fight cancer, block the PD-1/PD-L1 signaling pathway to kill cancer cells, and has the potential to treat many types of tumors
Libtayo uses Regeneron’s patented Velocimmune technology platform to create and optimize it.
Note: The original text has been deleted
Original source: Libtayo (cemiplimab) and chemotherapy first-line treatment combination significantly improved overall survival in patients with advanced NSCLC