Biomarkers for Monitoring Treatment Efficacy in Human Neurocysticercosis

Information

  • Research Project
  • 10134998
  • ApplicationId
    10134998
  • Core Project Number
    U19AI129909
  • Full Project Number
    5U19AI129909-05
  • Serial Number
    129909
  • FOA Number
    RFA-AI-16-002
  • Sub Project Id
    5712
  • Project Start Date
    4/15/2017 - 8 years ago
  • Project End Date
    3/31/2022 - 3 years ago
  • Program Officer Name
  • Budget Start Date
    4/1/2021 - 4 years ago
  • Budget End Date
    3/31/2022 - 3 years ago
  • Fiscal Year
    2021
  • Support Year
    05
  • Suffix
  • Award Notice Date
    4/1/2021 - 4 years ago

Biomarkers for Monitoring Treatment Efficacy in Human Neurocysticercosis

Peru-JHU TMRC Program Principal Investigator/Program Director (Last, First, Middle): GARCIA, Hector H. Component 2 - Biomarkers for Monitoring Treatment Efficacy in Human Neurocysticercosis PROJECT SUMMARY Human neurocysticercosis (NCC) is a frequent cause of seizures and other neurological disease in most developing countries also present in industrialized countries because of travel and immigration from endemic regions. Treatment of NCC involves symptomatic measures as well as interventions to destroy (antiparasitic treatment) or excise the parasites (surgical procedures). The efficacy of these interventions is usually monitored by neuroimaging techniques, computed tomography (CT) or magnetic resonance imaging (MRI), that are performed three or six months after treatment. The response rate to antiparasitic drugs is currently poor and the decision to retreat is frequently delayed until clinical relapse and/or obvious regrowth, which would be expected to lead to increased risk for complications and likely a more difficult course of retreatment. In addition, CT and MRI are expensive and not accessible in poor rural areas, where NCC is highly endemic. There is thus is an important need for an assay for early documentation of the response to therapy. Given the variability of clinical presentations of NCC, a single test or a time point in the follow up may not be the best choice for all scenarios. This component will attempt to develop one or more assays for early assessment of response to treatment in the main types of NCC, taking advantage of newly available test formats and our vast collection of archive samples in addition to additional prospectively collected baseline and post-treatment serum and urine samples to define a test, a sample and the time point of choice to better predict partial and complete responses to treatment for each of the main types of NCC.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    U19
  • Administering IC
    AI
  • Application Type
    5
  • Direct Cost Amount
    45300
  • Indirect Cost Amount
    3624
  • Total Cost
  • Sub Project Total Cost
    48924
  • ARRA Funded
    False
  • CFDA Code
  • Ed Inst. Type
  • Funding ICs
    NIAID:48924\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZAI1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSIDAD PERUANA CAYETANO HEREDIA
  • Organization Department
  • Organization DUNS
    934798430
  • Organization City
    LIMA
  • Organization State
  • Organization Country
    PERU
  • Organization Zip Code
    15102
  • Organization District
    PERU