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Merck (NYSE:MRK) stated on Thursday that its investigational coformulation for metastatic non-small cell lung most cancers (NSCLC) didn’t present an enchancment in median progression-free survival (PFS) in comparison with docetaxel alone – a clinically established chemotherapy medicine offered underneath title Taxotere by Sanofi-Aventis (NASDAQ:SNY).
In a non-registrational Section 2 KeyVibe-002 trial, vibostolimab/pembrolizumab plus docetaxel prolonged median PFS by 2.4 months in comparison with these handled with docetaxel alone, although the outcomes didn’t attain statistical significance (5.6 months vs. 3.2 months; HR=0.77 [95% CI, 0.53-1.13]; p=0.0910).
The coformulation, which included anti-TIGIT antibody vibostolimab and Merck’s anti-PD-1 remedy pembrolizumab (KEYTRUDA), additionally didn’t present an enchancment in median PFS alone in comparison with docetaxel alone.
As well as, the remedy didn’t present an enchancment in general survival in comparison with docetaxel alone. The protection profile of vibostolimab/pembrolizumab was per that noticed for vibostolimab and pembrolizumab in beforehand reported research, with no new security alerts noticed.
The trial assessed vibostolimab/pembrolizumab with or with out docetaxel versus placebo plus docetaxel in sufferers with metastatic NSCLC with progressive illness after therapy with immunotherapy and platinum-doublet chemotherapy.
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