From the outset, Genfit created a solid intellectual property framework, recognising that the protection of our assets and world-renowned academic research is key to the company’s value creation. 

INTELLECTUAL PROPERTY AT THE CORE OF GENFIT'S STRATEGY

Since its creation, Genfit has put in place a dedicated organisation in charge of establishing and preserving the Intellectual Property (IP) assets and supporting the strategic position and the development of the company.

The IP Department is responsible for pursuing the appropriate management and protection of IP assets that the company has generated through in-house research programs and collaborative research programs with both pharmaceutical and academic partners.

Today, the company has generated a large patent portfolio that covers strategic assets including novel chemical entities, pharmaceutical uses and compositions, biological materials, and diagnostic as well as research tools and methods.

 

A Selection of Genfit's Publications & Scientific Communications

A selection of Genfit's publications and scientific communications is listed below.

  • Phosphorylation of farnesoid X receptor by protein kinase C promotes its transcriptional activity
    Gineste R, Sirvent A, Paumelle R, Helleboid S, Aquilina A, Darteil R, Hum DW, Fruchart JC, Staels B.
    Mol Endocrinol. 2008 Nov; 22(11):2433-47
  • Systemic and Distal Repercussions of Liver-Specific Peroxisome Proliferator-Activated Receptor-{alpha} Control of the Acute-Phase Response
    Roxane M. Mansouri, Eric Baugé, Bart Staels, and Philippe Gervois
    Endocrinology, Jun 2008; 149: 3215 - 3223
  • ChREBP, but not LXRs, is required for the induction of glucose-regulated genes in liver
    Pierre-Damien Denechaud, Pascale Bossard, Jean-Marc A. Lobaccaro, Lesley Millatt, Bart Staels, Jean Girard, and Catherine Postic
    Journal of Clinical Investigation, March 2008; 118 (3) 956-964
  • Changes in gene expression in skeletal muscle in response to fat overfeeding in lean men
    E. Meugnier - C. Bossu - M. Oliel - S. Jeanne - A. Michaut - M. Sothier - J. Brozek - S. Rome - M. Laville - H. Vidal
    Obesity, 2007, 15 (11), p. 2583
  • Safety issues and prospects for future generations of PPAR modulators
    Anne Rubenstrunk, Rémy Hanf, Dean W. Hum, Jean-Charles Fruchart, Bart Staels
    BBA - Molecular and Cell Biology of Lipids, Aug 2007; 1771(8): 1065-81
  • PPARgamma activation primes human monocytes into alternative M2 macrophages with anti-inflammatory properties
    Bouhlel MA, Derudas B, Rigamonti E, Dièvart R, Brozek J, Haulon S, Zawadzki C, Jude B, Torpier G, Marx N, Staels B, Chinetti-Gbaguidi G.
    Cell Metab. 2007 Aug;6(2):96-8
  • TReP-132 is a novel progesterone receptor coactivator required for the inhibition of breast cancer cell growth and enhancement of differentiation by progesterone
    Gizard F, Robillard R, Gross B, Barbier O, Révillion F, Peyrat JP, Torpier G, Hum DW, Staels B.
    Mol. Cell. Biol. 2006; 26: 7632-7644
  • Protein kinase C pathway promotes Farnesoid X Receptor transcriptional activity
    R.Gineste, A.Sirvent, R. Paumelle, A. Aquilina, S.Helleboid, R.Darteil, DW.Hum, JC. Fruchart, B.Staels
    2006.08.29 Med Chem - FXR – CM
  • Early Diet-induced non-alcoholic steatohepatitis in APOE2 knock-in mice and its prevention by fibrates
    R. Shiri-Sverdlov - K. Wouters - P. J. Van Gorp - M. J. Gijbels - B. Noêl - L. Buffat - B,.Staels -N. Maeda - M. van Bilsen - M. H. Hofker
    J Hepatol. 2006-Apr;44(4):732-41
  • Sorting out the roles of PPARa in energy metabolism and vascular homeostasis
    Lefebvre P, Chinetti G, Fruchart JC and Staels B
    The Journal of Clinical Investigation, 2006, 116 (3), 571-581
  • Effects of Niacin on plasma lipids of wild type and PPARa-KO mice
    R. Hanf , A. Rubenstrunk, F. Contard and JC Fruchart
    EASD 2006
  • The Neuroprotective Effect of Atorvastatin in a Murine MCAO Model Is Dependent on PPARalpha
    Sayah-Jeanne S, Bordet R, Laprais M, Poulain P, Coussaert A, Duriez P, Hanf R, Laskey R, Sasiela W, Hum D, Staels B and Fruchart JC
    Stroke. 2006 Feb. 37(2)P432
  • Role of the PPAR family of nuclear receptors in the regulation of metabolic and cardiovascular homeostasis: new approaches to therapy
    Chinetti-Gbaguidi G, Fruchart JC and Staels B
    Curr Opin Pharmacol, 2005, 5 (2), 177-83 
  • Peroxisome Proliferator-Activated Receptor b/d: A novel target for the reduction of atherosclerosis
    Gross BS, Fruchart JC and Staels B
    Drug Discovery Today: Therapeutic Strategies, 2005, 2 (3), 237-243
  • Regulation of human apoA-I by gemfibrozil and fenofibrate through selective peroxisome proliferator-activated receptor alpha modulation
    Duez H, Lefebvre B, Poulain P, Torra IP, Percevault F, Luc G, Peters JM, Gonzalez FJ, Gineste R, Helleboid S, Dzavik V, Fruchart JC, Fievet C, Lefebvre P and Staels B
    Arterioscler Thromb Vasc Biol, 2005, 25 (3), 585-91 
  • TReP-132 controls cell proliferation by regulating the expression of the cyclin-dependent kinase inhibitors p21WAF1/Cip1 and p27Kip1
    Gizard F, Robillard R, Barbier O, Quatannens B, Faucompre A, Revillion F, Peyrat JP, Staels B and Hum DW
    Mol Cell Biol, 2005, 25 (11), 4335-48 
  • Progesterone inhibits human breast cancer cell growth through transcriptional upregulation of the cyclin-dependent kinase inhibitor p27Kip1 gene
    Gizard F, Robillard R, Gervois P, Faucompre A, Revillion F, Peyrat JP, Hum WD and Staels B
    FEBS Lett, 2005, 579 (25), 5535-41
  • Molecular characterization of new selective peroxisome proliferator-activated receptor gamma modulators with angiotensin receptor blocking activity
    Schupp M, Clemenz M, Gineste R, Witt H, Janke J, Helleboid S, Hennuyer N, Ruiz P, Unger T, Staels B and Kintscher U
    Diabetes, 2005, 54 (12), 3442-52 
  • PPARgamma activating angiotensin receptor blockers exhibit differential cofactor recruitment and induce a divergent gene expression profile in 3T3-L1 adipocytes
    Schupp M, Gineste R, Clemenz M, Witt H, Janke J, Helleboid S, Hennuyer N, Ruiz P, Unger T, Staels B and Kintscher U
    3rd International Symposium on PPARs efficacy and safety - Abstract book, 2005
  • Farnesoid X receptor represses hepatic lipase gene expression
    Sirvent A, Verhoeven AJ, Jansen H, Kosykh V, Darteil RJ, Hum DW, Fruchart JC and Staels B
    J Lipid Res, 2004, 45 (11), 2110-5 
  • The farnesoid X receptor induces very low density lipoprotein receptor gene expression
    Sirvent A, Claudel T, Martin G, Brozek J, Kosykh V, Darteil R, Hum DW, Fruchart JC and Staels B
    FEBS Lett, 2004, 566 (1-3), 173-7