Nov 22 (Reuters) - Lexicon Pharmaceuticals ( LXRX ) said
on Friday it would reduce its workforce by about 60%, after the
U.S. Food and Drug Administration noted deficiencies in its
application seeking approval for its diabetes drug.
This comes days after a panel of advisers to the FDA
voted against recommending the drug, sotagliflozin, as an add-on
treatment to insulin therapy for managing blood glucose levels
in adults with type 1 diabetes and chronic kidney disease.
Shares of the biopharma firm were down nearly 12% at 68
cents in premarket trading.
Lexicon said it will eliminate its commercial field team and
stop promotional efforts for its approved heart failure
treatment, Inpefa.
However, the company said it will continue to
manufacture and make Inpefa available to patients and existing
prescribers.
As part of the restructuring, Lexicon aims to reduce
operating costs by $100 million in 2025.