A combination product containing Merck & Co., Inc.’s Keytruda plus its investigational anti-TIGIT therapy, vibostolimab, has missed the mark in a Phase II lung cancer trial, adding to a spate of disappointments in the TIGIT space, but some analysts remain hopeful about performance in earlier lines of disease.
The US major product candidate, known as MK-7684A, is a coformulation of 200mg of its blockbuster anti-PD-L1 drug Keytruda (pembrolizumab) and 200mg/20mL of its anti-TIGIT asset, vibostolimab.
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