Drug Discovery for Neurodegeneration
Drug Discovery for Neurodegeneration
批准号:
7806086
负责人:
Howard M. Fillit
金额:
$4.0万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-15 至 2009-08-31
关键词:
AcademiaAddressAlzheimer&aposs DiseaseAmyotrophic Lateral SclerosisAreaBasic ScienceDevelopmentDisciplineDiseaseDistrict of ColumbiaDrug IndustryEducationFoundationsGoalsGrantHuntington DiseaseIncidenceIndustryInformation ResourcesJournalsKnowledgeLearningMinorityNerve DegenerationNeurodegenerative DisordersOrphanParkinson DiseaseParticipantPeer ReviewPharmaceutical ChemistryPharmaceutical PreparationsPhaseProcessPublic HealthPublishingResearchResearch PersonnelResourcesScheduleScientistServicesTechnology TransferTimeTrainingTranslatingU-Series Cooperative AgreementsUnited States National Institutes of HealthWomanWorkdrug discoverygraduate studentmeetingsnervous system disordernext generationnovel therapeuticspre-clinicalpreventprogramspublic health relevancepublic-private partnershipskillssymposium
中文摘要
描述(由申请人提供):阿尔茨海默病药物发现基金会(ADDF)要求U13合作协议赠款,以支持其神经变性药物发现会议,定于2009年2月9日至10日在华盛顿,DC。会议的目的是通过培训下一代科学领导人将基础研究转化为新疗法的过程来推进神经退行性疾病的药物发现。需要关于这一主题的正规教育,因为在这一研究领域存在有据可查的知识差距,而且在制药行业之外很少有机会了解这些过程。这次教学会议的目标显然与NIH的路线图一致:弥合药物发现和神经退行性疾病的知识差距;汇集跨学科科学家,以刺激结合技能和学科的新方法;为这些科学家提供交流思想和资源的网络机会;并最终在同行评审的开放获取科学期刊上发表论文。这个为期两天的会议将为与会者提供关于创造治疗和预防神经退行性疾病新药的基本知识和资源。它将解决与以下子主题相关的障碍和挑战:药物化学的基础知识;命中和线索:药物发现的早期阶段;临床前概念验证和开发;技术转让问题;询问专家(分组会议);推进药物发现的资源和服务。阿尔茨海默病、帕金森病、亨廷顿病、肌萎缩侧索硬化症和“孤儿”神经系统疾病将被列入该计划。会议将包括3到5个演讲,有足够的时间进行问答。关于路线图的公私伙伴关系倡议,ADDF将邀请来自学术界、工业界和NIH的26名国际知名科学家担任主席或发言人。预计这次会议将为来自不同背景的150名科学家提供服务,包括妇女、少数民族、年轻/初级研究人员和研究生。
公共卫生相关性:ADDF寻求解决的公共卫生问题是减少神经退行性疾病的发病率,如阿尔茨海默病、帕金森病、亨廷顿病和肌萎缩性侧索硬化症。通过举办这次会议,ADDF将增加科学家对药物发现过程的了解,并促进他们共同开发商业上可行和有效的疾病修饰疗法。
英文摘要
DESCRIPTION (provided by applicant): The Alzheimer's Drug Discovery Foundation (ADDF) requests a U13 Cooperative Agreement grant in support of its Drug Discovery for Neurodegeneration conference, scheduled for February 9-10, 2009 in Washington, DC. The purpose of the meeting is to advance drug discovery for neurodegenerative disease by training the next generation of scientific leaders on the process of translating basic research into novel therapeutics. Formal education on this topic is needed because there is a documented knowledge gap in this area of research and there are very few opportunities outside of the pharmaceutical industry to learn about these processes. The goals of this didactic conference are clearly consistent with the NIH's Roadmap: to bridge the knowledge gap in drug discovery and neurodegenerative disease; to bring together interdisciplinary scientists to stimulate new ways of combining skills and disciplines; to provide networking opportunities for these scientists to exchange ideas and resources; and to ultimately publish the proceedings in a peer-reviewed, open access scientific journal. This two-day conference will give participants fundamental knowledge and resources on creating new drugs to treat and prevent neurodegenerative disease. It will address the barriers and challenges associated with the following sub-topics: Basics of Medicinal Chemistry; Hits & Leads: Early Phases of Drug Discovery; Pre-Clinical Proof-of-Concept & Development; Issues in Technology Transfer; Ask the Experts (breakout session); and Resources and Services for Advancing Drug Discovery. Alzheimer's disease, Parkinson's disease, Huntington's disease, Amyotrophic Lateral Sclerosis and 'Orphan' neurological diseases will be included in the program. Sessions will consist of 3 to 5 presentations with ample time for Q&A. With respect to the public-private partnership initiative of the Roadmap, ADDF will invite 26 internationally recognized scientists from academia, industry and NIH to serve as chairs or speakers. It is anticipated that this conference will serve 150 scientists from diverse backgrounds, including women, minorities, young/junior investigators and graduate students.
PUBLIC HEALTH RELEVANCE: The public health problem ADDF seeks to solve is to reduce the incidence of neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, Huntington's disease and Amyotrophic Lateral Sclerosis. By offering this conference, ADDF will increase scientists' knowledge of the drug discovery processes and catalyze them to work together to develop commercially viable and effective disease modifying therapies.
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会议论文
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依托单位:
SPECIFICITY OF HUMAN AUTOANTIBODIES TO PROTEOGLYCANS
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依托单位:
SPECIFICITY OF HUMAN AUTOANTIBODIES TO PROTEOGLYCANS
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项目类别:
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海外基金