Authorization

Preclinical study of GKT831 shows rapid regression of cholestatic fibrosis in model of advanced liver fibrosis

Data consistent with anti-fibrotic activity recently demonstrated in PBC Phase 2 trial of GKT831



Data further support broad therapeutic potential of GKT831 in multiple fibrotic diseases

ARCHAMPS, France, May 21, 2019 (GLOBE NEWSWIRE) -- Genkyotex (Euronext Paris & Brussels: FR0013399474 a?? GKTX), a biopharmaceutical company and the leader in NOX therapies, today announced the publication of preclinical efficacy data with GKT831 for cholestatic fibrosis. The article a??Activated Hepatic Stellate Cells and Portal Fibroblasts contribute to cholestatic liver fibrosis in MDR2 knockout micea?? was published in the Journal of Hepatology1.
These preclinical results are consistent with the reduction in liver stiffness achieved in Phase 2 with GKT831 after just 24 weeks of treatment in PBC patients. In patients with an estimated F score of F3 (severe) or greater, GKT831 achieved a 21% reduction in liver stiffness. In the 400mg BID dose, GKT831 achieved an absolute reduction of 2.7 kPa compared to an increase of 0.4 kPa for the placebo group.Philippe WIesel, CMO of Genkyotex, commented: a??The MDR2 KO mouse model is the most relevant model of advanced cholestatic fibrosis and is particularly relevant to human diseases like PBC and PSC where patients develop severe fibrosis. The data indicate that GKT831 achieves rapid fibrosis reversal which is in line with the clinical evidence of anti-fibrotic activity obtained in our 24-week PBC trial.a??A AIn the MDR2 KO mouse model, GKT831 treatment was initiated at week 12 when advanced liver fibrosis was already established. After only 4 weeks of treatment, GKT831 was able to deactivate myofibroblasts and reverse fibrosis, indicating rapid anti-fibrotic activity.GKT831 had already shown marked efficacy in multiple mouse models of inflammatory and fibrotic disorders.
About GenkyotexGenkyotex is the leading biopharmaceutical company in NOX therapies, listed on the Euronext Paris and Euronext Brussels markets. A leader in NOX therapies, its unique therapeutic approach is based on a selective inhibition of NOX enzymes that amplify multiple disease processes such as fibrosis, inflammation, pain processing, cancer development, and neurodegeneration.Genkyotexa??s platform enables the identification of orally available small-molecules that selectively inhibit specific NOX enzymes. Genkyotex is developing a pipeline of first-in-class product candidates targeting one or multiple NOX enzymes. The lead product candidate, GKT831, a NOX1 and NOX4 inhibitor is evaluated in a phase 2 clinical trial in primary biliary cholangitis (PBC, a fibrotic orphan disease) and in an investigator-initiated Phase 2 clinical trial in Type 1 Diabetes and Kidney Disease (DKD). A grant from the United States National Institutes of Health (NIH) of $8.9 million was awarded to Professor Victor Thannickal at the University of Alabama at Birmingham (UAB) to fund a multi-year research program evaluating the role of NOX enzymes in idiopathic pulmonary fibrosis (IPF), a chronic lung disease that results in fibrosis of the lungs, the core component of the program will be to conduct a Phase 2 trial with the GKT831 in patients with IPF. This product candidate may also be active in other fibrotic indications. Genkyotex also has a versatile platform well-suited to the development of various immunotherapies (Vaxiclase). A partnership covering the use of Vaxiclase as an antigen per se (GTL003) has been established with Serum Institute of India Private Ltd (Serum Institute), the worlda??s largest producer of vaccine doses, for the development by Serum Institute of cellular multivalent combination vaccines against a variety of infectious diseases. For further information, please go towww.genkyotex.com. or investors@genkyotex.comDisclaimerThis press release may contain forward-looking statements by the company with respect to its objectives. Such statements are based upon the current beliefs, estimates and expectations of Genkyotexa??s management and are subject to risks and uncertainties such as the company's ability to implement its chosen strategy, customer market trends, changes in technologies and in the company's competitive environment, changes in regulations, clinical or industrial risks and all risks linked to the company's growth. These factors as well as other risks and uncertainties may prevent the company from achieving the objectives outlined in the press release and actual results may differ from those set forth in the forward-looking statements, due to various factors. Without being exhaustive, such factors include uncertainties involved in the development of Genkyotexa??s products, which may not succeed, or in the delivery of Genkyotexa??s products marketing authorizations by the relevant regulatory authorities and, in general, any factor that could affects Genkyotexa??s capacity to commercialize the products it develops. No guarantee is given on forward-looking statements which are subject to a number of risks, notably those described in the registration document (document de reference) registered by the French Markets Authority (the AMF) on 26 April 2019 under number R.19-014, and those linked to changes in economic conditions, the financial markets, or the markets on which Genkyotex is present. Genkyotex products are currently used for clinical trials only and are not otherwise available for distribution or sale.

Media relationsA A A A A A A A A A A A A A A A
Sophie BaumontA A A A A A A A A A A A A A A
LifeSci AdvisorsA A A A A A A A
+33 6 2774 74 49A A A A A A A A A A A A A A A
sophie@lifesciadvisors.com



Investor relations
Brian Ritchie
LifeSci Advisors, LCC
+1 212 915 2578
britchie@lifesciadvisors.com

1ANishio T, Hu R, Koyama Y, Liang S, Rosenthal SB, Yamamoto G, Karin D, Baglieri J, Ma HY, Xu J, Liu X, Dhar D, Iwaisako K, Taura K, Brenner DA, Kisseleva T. Activated Hepatic Stellate Cells and Portal Fibroblasts contribute to cholestatic liver fibrosis in MDR2 knockout mice. J Hepatol. 2019 May 6. pii: S0168-8278(19)30273-9. doi: 10.1016/j.jhep.2019.04.012. [Epub ahead of print]
See also:
Leave a comment
News
  • Latest
  • Read
  • Commented
Calendar Content
«     2019    »
 12
3456789
10111213141516
17181920212223
24252627282930