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GENFIT (ALGFT) Initiates Pediatric NAFLD/NASH Program In Europe Further To The Approval Of Elafibranor’s Pediatric Investigation Plan By The EMA



11/14/2016 9:46:12 AM

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› Elafibranor’s Pediatric Investigation Plan (PIP) approved by the European Medicine Agency (EMA) for the Treatment of non-alcoholic fatty liver disease (NAFLD) including non-alcoholic steatohepatitis (NASH)

› First studies started further to the opinion formulated by the Paediatric Committee of the EMA

› No concerns on potential long term safety/efficacy issues in relation to paediatric use in children from 2 to 18 years of age

Lille (France), Cambridge (Massachusetts, United States), November 14, 2016 – GENFIT (Euronext: GNFT - ISIN: FR0004163111), a biopharmaceutical company at the forefront of developing therapeutic and diagnostic solutions in metabolic and inflammatory diseases, that notably affect the liver or the gastrointestinal system, today announced that the company has initiated its program in paediatric NAFLD/NASH.

This key step follows the approval by the European Medicine Agency (EMA) of elafibranor’s Pediatric Investigation Plan (PIP).

Due to its good safety/efficacy profile demonstrated in adults in Phase2b, elafibranor presents a promising potential to treat children from 2 to 18 years of age.

Dr. Joel Lavine, MD, PhD, Co-Chair NASH CRN (NIDDK), Professor & Vice-Chair (Research), Department of Pediatrics Chief, Pediatric GI/Hepatology/Nutrition, Columbia University, NY, USA commented: “Pediatric NAFLD is an alcohol-like disease of the liver that develops in children who drink no or little alcohol. Prevalence is quite high in general, with boys, obese, and patients of certain Hispanic origins being particularly affected. In addition to the higher prevalence associated with age, there is also a strong association between metabolic syndrome and liver histologic severity among children with NAFLD. It’s very exciting to see elafibranor being given a green light by the European regulatory agency to proceed further with trials in this critical space. The efficacy and safety profile renders this drug a very promising therapy.”

Sophie Mégnien, Chief Medical Officer (CMO) of GENFIT commented: “We are very pleased today to develop a plan for children requiring treatment of their NAFLD/NASH. Juvenile toxicology studies are ongoing and we all look forward to similar steps in the US, given the encouraging results seen in adults in the Phase 2b trial. Due to the very good tolerability and safety profile of elafibranor, and given the efficacy it has demonstrated in adults earlier, we are confident in the potential of the molecule to address key unmet needs in children and teenagers.”

About elafibranor:

Elafibranor is GENFIT’s lead pipeline product. Elafibranor is an oral once-daily treatment, and a first-in-class drug acting via dual peroxisome proliferator-activated alpha/delta pathways developed to treat, in particular, nonalcoholic steatohepatitis (NASH). Elafibranor is believed to address multiple facets of NASH, including inflammation, insulin sensitivity, lipid/metabolic profile, and liver markers.

About NASH:

“NASH”, or nonalcoholic steatohepatitis, is a liver disease characterized by an accumulation of fat (lipid droplets), along with inflammation and degeneration of hepatocytes. The disease is associated with long term risk of progression to cirrhosis, a state where liver function is diminished, leading to liver insufficiency, and also progression to liver cancer.

About GENFIT:

GENFIT is a biopharmaceutical company focused on the discovery and development of drug candidates in areas of high unmet medical needs corresponding to a lack of suitable treatment and an increasing number of patients worldwide. GENFIT’s R&D efforts are focused on bringing new medicines to market for patients with metabolic, inflammatory, autoimmune and fibrotic diseases, that affect the liver (such as NASH – Nonalcoholic steatohepatitis) and more generally the gastro-intestinal arena. GENFIT’s approach combines novel treatments and biomarkers. Its lead proprietary compound, elafibranor, is currently in a Phase 3 study. With facilities in Lille and Paris, France, and Cambridge, MA (USA), the Company has approximately 110 employees. GENFIT is a public company listed in compartment B of Euronext’s regulated market in Paris (Euronext: GNFT - ISIN: FR0004163111). www.genfit.com

Read at BioSpace.com


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