Sanofi slashes another program for key molecule, while keeping hopes in handful of rare diseases
Several years ago, when Sanofi unveiled a molecule to prevent the accumulation of a certain type of fat in cells, they figured it would work in a handful of rare diseases where the body can’t properly clear toxic chemicals. But they also had hopes and some biological intuition that it might provide a new way of treating a couple of larger disorders.
Those hopes have now come up empty. Sanofi announced Tuesday that it scrapped a pivotal trial for the molecule, venglustat, in autosomal polycystic dominant kidney disease — the most common form of inherited kidney disease — after an independent review showed little difference between patients on the drug arm and patients on the placebo.
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