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中文摘要
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DESCRIPTION (provided by applicant): Influenza is a highly infectious acute respiratory viral disease that is characterized by recurrent annual epidemics and periodic major worldwide pandemics. Outbreaks are caused by infection of the highly diverse and mutable influenza viruses A and B (IFV A & IFV B). Novel broad-spectrum prophylaxis and therapeutics are critically needed to address the annual influenza epidemics and the escalating threat of pandemic influenza. NexBio has created a novel recombinant fusion protein-based anti-IFV agent, referred to as Fludase(r). Distinct from conventional vaccines and antivirals, Fludase(r) works by eliminating influenza virus receptors on the airway surface. It potentially confers broad-spectrum protection against all subtypes and strains of influenza viruses without the need for annual updates. Fludase(r) also has several built-in features to enable long drug retention on the airway surface and was engineered to be nonimmunogenic in humans. In the last 2 years, NexBio has finalized the molecular sequence of Fludase(r) and demonstrated its broad and potent anti-IFV efficacy in tissue culture and in two animal models. These accomplishments have provided strong justification for further developmental studies of Fludase(r). During the recent pre-IND meeting, the FDA raised several preclinical questions and indicated that as a first-in-class drug candidate, a thorough understanding of the Fludase(r) safety issues and mechanism of action is necessary. The main focus of this Challenge Grant proposal is to address the FDA's specific requests. Additionally, this grant proposal addresses new and important issues arising from Fludase(r) analytical and manufacture development.
期刊论文(4)
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会议论文
DOI: 10.1371/journal.pone.0007838
发表时间: 2009-11-06
期刊: PloS one
影响因子: 3.7
作者: [Triana-Baltzer GB, Gubareva LV, Klimov AI, Wurtman DF, Moss RB, Hedlund M, Larson JL, Belshe RB, Fang F]
通讯作者: Fang F
DOI: 10.3390/v2081766
发表时间: 2010-08
期刊: Viruses
影响因子: --
作者: [Hedlund M, Larson JL, Fang F]
通讯作者: Fang F
DOI: 10.1086/651170
发表时间: 2010-04-01
期刊: The Journal of infectious diseases
影响因子: --
作者: [Hedlund M, Aschenbrenner LM, Jensen K, Larson JL, Fang F]
通讯作者: Fang F
STRUCTURE DETERMINATION OF RV2996C/NADH, AND RV2513
  • 批准号:
    7598267
  • 项目类别:
  • 资助金额:
    $0.02万
  • 财政年份:
    2007
  • 负责人:
    MANG YU
  • 依托单位:
Development of DAS181 (Fludase^) as a Broad Spectrum Therapeutic Agent
  • 批准号:
    8020431
  • 项目类别:
  • 资助金额:
    $999.92万
  • 财政年份:
    2006
  • 负责人:
    MANG YU
  • 依托单位:
Development of Fludase as an Anti-Influenza Agent
  • 批准号:
    7269392
  • 项目类别:
  • 资助金额:
    $101.57万
  • 财政年份:
    2006
  • 负责人:
    MANG YU
  • 依托单位:
Development of Fludase as an Anti-Influenza Agent
  • 批准号:
    7133666
  • 项目类别:
  • 资助金额:
    $187.14万
  • 财政年份:
    2006
  • 负责人:
    MANG YU
  • 依托单位:
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