PDGFR and KDR Inhibitors for Liver Fibrosis

Information

  • Research Project
  • 8833470
  • ApplicationId
    8833470
  • Core Project Number
    R44DK085771
  • Full Project Number
    2R44DK085771-02A1
  • Serial Number
    085771
  • FOA Number
    PA-14-071
  • Sub Project Id
  • Project Start Date
    6/7/2010 - 14 years ago
  • Project End Date
    8/31/2016 - 7 years ago
  • Program Officer Name
    DENSMORE, CHRISTINE L
  • Budget Start Date
    9/15/2014 - 9 years ago
  • Budget End Date
    8/31/2016 - 7 years ago
  • Fiscal Year
    2014
  • Support Year
    02
  • Suffix
    A1
  • Award Notice Date
    9/8/2014 - 9 years ago
Organizations

PDGFR and KDR Inhibitors for Liver Fibrosis

? DESCRIPTION (provided by applicant): The incidence and prevalence of both alcoholic and non-alcoholic liver diseases is increasing. The population presenting with Metabolic Syndrome, a key risk factor for NAFLD-NASH-liver fibrosis is ballooning. Left untreated, liver fibrosis can progress to cirrhosis or end-stage liver disease and even hepatocellular carcinoma. Today, therapeutic strategies are primarily geared toward mitigating NAFLD-NASH via diet modification, exercise and medication. Unfortunately, there is no approved therapy for established liver fibrosis other than organ transplantation. The proposed translational research program is designed to bring to clinical trials an outstanding and highly promising orally bioavailable small molecule antifibrotic to clinical trials for the treatment of liver fibrosis. Anion Biomedica has identified ANG3070, a potent, highly water-soluble, orally bioavailable, small molecule platelet-derived growth factor receptor (PDGFR) and vascular endothelial growth factor receptor (KDR) inhibitor. Highly compelling data in two models of liver disease speak to antifibrotic activity of this drug candidate. Furthermore, funding for the suite of Investigational New Drug (IND)-enabling safety studies for this drug candidate has been appropriated from the NIH and DoD. The proposed SBIR Phase II program seeks to obtain dose efficacy information for ANG3070 in two dietary models of liver disease which simulate to some extent the human NAFLD-NASH-liver fibrosis phenotype. Efficacy data from this study, together with the safety data will determine drug therapeutic index and form the form the basis of an IND submission to FDA to bring this drug to clinical trials. 1

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R44
  • Administering IC
    DK
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    769978
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
    NIDDK:769978\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ANGION BIOMEDICA CORPORATION
  • Organization Department
  • Organization DUNS
    053129065
  • Organization City
    UNIONDALE
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    115533658
  • Organization District
    UNITED STATES