Lexicon Pharmaceuticals reported a net loss of $44.9 million, or $0.22 per share, for the second quarter of 2023. The company received FDA approval for INPEFA and commercially launched it in the U.S. LX9211 is moving into late-stage development for diabetic peripheral neuropathic pain.
INPEFA (sotagliflozin) received FDA approval for the treatment of heart failure.
INPEFA was granted a broad label across the full range of left ventricular ejection fraction, including HFpEF and HFrEF, and for patients with or without diabetes.
LX9211 is moving into late-stage development for the treatment of diabetic peripheral neuropathic pain.
Lexicon commercially launched INPEFA in the U.S. within 30 days of FDA approval.
This press release contains forward-looking statements relating to Lexicon’s financial position and long-term outlook on its business, including the commercialization of its approved products and the clinical development of, regulatory filings for, and potential therapeutic and commercial potential of its other drug candidates.
Visualization of income flow from segment revenue to net income