Inventiva announces that its IND application for the Phase II combination trial with lanifibranor and empagliflozin in patients with NASH and T2D has been accepted by the FDA
Daix (France), Long Island City (New York, United States), March 8, 2022 – Inventiva (Euronext Paris and Nasdaq: IVA), a clinical-stage biopharmaceutical company focused on the development of oral small molecule therapies for the treatment of non-alcoholic steatohepatitis (NASH) and other diseases with significant unmet medical needs, today announced that the U.S. Food and Drug Administration (FDA) has completed its safety review of the IND application and has concluded that the proof-of-concept Phase II combination trial with its lead drug candidate lanifibranor and the SGLT2 inhibitor empagliflozin1 in patients with Type 2 Diabetes (T2D) and non- cirrhotic NASH may proceed.
Pierre Broqua, Chief Scientist Officer and cofounder of Inventiva, stated: “The FDA’s decision to clear our Investigational New Drug submitted for our proof-of–concept study, LEGEND, is an important milestone for the development of lanifibranor. Our Phase IIb2 has successfully demonstrated that lanifibranor as a monotherapy could not only resolve NASH and improve fibrosis but also improve the lipids and glycemic profiles. We believe that a combination therapy with lanifibranor and empagliflozin can provide additional benefits and further improve the cardiometabolic risk profile of patients with NASH.”
Dr. Onno Holleboom, Internist and endocrinologist at Amsterdam University Medical Centers and co-Principal Investigator of LEGEND: “As a pan-PPAR agonist acting on the key components of NASH: metabolism, inflammation and fibrosis, lanifibranor is a good candidate for a first-line pharmacology treatment for NASH. However, NASH is a multifaceted disease and the treatment of NASH will naturally evolve to include combination therapies in order to address the full cardiometabolic spectrum of the disease. Combination therapies allow to individualize treatment and improve clinical management of patients and I am excited to assess whether lanifibranor and empagliflozin could potentially lead to such results for patients with T2D and NASH.”
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