Translational Development of Glial Growth Factor 2 (GGF2) for the Treatment of St

Information

  • Research Project
  • 8927076
  • ApplicationId
    8927076
  • Core Project Number
    U01NS076474
  • Full Project Number
    5U01NS076474-02
  • Serial Number
    076474
  • FOA Number
    PAR-13-022
  • Sub Project Id
  • Project Start Date
    9/15/2014 - 10 years ago
  • Project End Date
    7/31/2019 - 5 years ago
  • Program Officer Name
    MCGAVERN, LINDA
  • Budget Start Date
    8/1/2016 - 8 years ago
  • Budget End Date
    7/31/2017 - 7 years ago
  • Fiscal Year
    2016
  • Support Year
    02
  • Suffix
  • Award Notice Date
    9/2/2016 - 8 years ago
Organizations

Translational Development of Glial Growth Factor 2 (GGF2) for the Treatment of St

DESCRIPTION (provided by applicant): Abstract Approximately 800,000 individuals suffer a stroke each year in the United States. Development of Glial Growth Factor 2 (GGF2) for promotion of stroke recovery is significant because of the lack of therapeutics to treat stroke. GGF2 also has a very wide treatment window (days) because it is not dependent upon neuroprotection. Additionally, as GGF2 is already in clinical trials for another indication, barries to manufacturing, formulation and toxicology have either been eliminated, or greatly reduced. The innovative aspect of this application comes from leveraging the existing development work that has been completed with GGF2 for another indication to efficiently enable an IND for stroke. Expanding on a significant body of preclinical data, GGF2 dosing will be optimized in a rat middle cerebral artery occlusion (MCAO) stroke model. Studies will explore dose frequency, extended dose duration and determine permanence of effects. Additional toxicology will be performed to enable the specific dose regimen proposed for stroke. GGF2 efficacy will then be confirmed in an established non-human primate model of cortical ischemia using a gyrencephalic rhesus monkey model. This model emphasizes neurorecovery rather than lesion volume reduction. Dosing will begin 24 hours after ischemia and behavioral improvements will be followed for at least 8 weeks in both rat and monkey studies. Following completion of studies in rhesus monkey an IND will be filed with the FDA.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    U01
  • Administering IC
    NS
  • Application Type
    5
  • Direct Cost Amount
    889483
  • Indirect Cost Amount
    494
  • Total Cost
    889977
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:889977\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    NSD
  • Study Section Name
    National Institute of Neurological Disorders and Stroke Initial Review Group
  • Organization Name
    ACORDA THERAPEUTICS, INC.
  • Organization Department
  • Organization DUNS
    963845136
  • Organization City
    ARDSLEY
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    105022605
  • Organization District
    UNITED STATES