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BPCA PHARMACOEPIDEMIOLOGY (REAL WORLD DATA) STUDIES

BPCA PHARMACOEPIDEMIOLOGY (REAL WORLD DATA) STUDIES
BPCA 药物流行病学(真实世界数据)研究
批准号:
10475400
负责人:
KANECIA ZIMMERMAN
金额:
$60.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-08-16 至 2025-08-15

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中文摘要
翻译
自20世纪90年代初以来,科学界,包括学术界,NIH,FDA和 制药业一直致力于提高药物的知识, 孩子国会已经通过立法,为药物开发计划提供激励措施, 儿科.负责实施和监督改进药品 儿科的开发主要委托给FDA(专利药物), 美国国立卫生研究院(非专利药物)。尽管立法增加了 在儿童中进行的临床研究中,在发育等领域仍然存在差距, 药理学,药物代谢的个体发生,结果测量的验证, 儿科研究的终点,最近利用数据库和电子健康 记录(真实的世界健康数据),以利用临床研究。经过30多年的 立法,面对临床护理和研究方面的迅速发展的技术进步, 很明显,要继续成功地缩小在以下领域的知识差距, 儿科药物开发,以适当地治疗儿科患者的各种疾病, 需要对儿科药物开发研究采取综合和全面的方法。 此外,NICHD和科学界的其他人得出结论, 临床研究数据的协调(即,PK、药效学、药物基因组学, 有效性和安全性数据),使用现有临床相关数据库、登记研究和 整理真实的世界患者健康数据的其他方法对于有效地 以个性化的方式治疗儿科患者。
英文摘要
Since the early 1990s, the scientific community, including academia, NIH, FDA and the pharmaceutical industry have worked to improve the knowledge of medications used in children. Congress has passed legislations to provide incentives for drug development plans in pediatrics. The responsibility for the implementation and oversight for improving drug development in pediatrics has been delegated primarily to the FDA (for on-patent drugs) and to the NIH (for off-patent drugs). Even though the legislations have improved the number of clinical studies conducted in children, gaps remain in areas such as developmental pharmacology, ontogeny of drug metabolism, the validation of outcome measures and endpoints in pediatric research, and most recently utilizing databases and electronic health records (real world health data) to leverage clinical research. After more than 30 years of legislation, and in the face of burgeoning technological advances in clinical care and research, it has become clear that to be successful in continuing to close knowledge gaps in the area of pediatric drug development to appropriately treat pediatric patients for a variety of diseases, an integrated and comprehensive approach to pediatric drug development research is required. Furthermore, NICHD and others in the scientific community are concluding that the harmonization of clinical research data (i.e., PK, pharmacodynamic, pharmacogenomic, efficiency, and safety data) with the use of existing clinically relevant databases, registries and other means of collating real world patient health data are vital to the success of effectively treating pediatric patients in a personalized way.
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PTN, PHARMACEUTICALS (PK) AND SAFETY OF COMMONLY USED DRUGS IN LACTATING WOMEN AND BREASTFED INFANTS (CUDDLE 2.0) NETWORK
  • 批准号:
    10495378
  • 项目类别:
  • 资助金额:
    $41.62万
  • 财政年份:
    2021
  • 负责人:
    KANECIA ZIMMERMAN
  • 依托单位:
BPCA INNOVATIVE TRIAL DESIGNS FOR DOSING, SAFETY, AND EFFICACY IN PEDIATRIC THERAPEUTICS
  • 批准号:
    10267019
  • 项目类别:
  • 资助金额:
    $34.92万
  • 财政年份:
    2019
  • 负责人:
    KANECIA ZIMMERMAN
  • 依托单位:
BPCA INNOVATIVE TRIAL DESIGNS FOR DOSING, SAFETY, AND EFFICACY IN PEDIATRIC THERAPEUTICS
  • 批准号:
    10019016
  • 项目类别:
  • 资助金额:
    $1.57万
  • 财政年份:
    2019
  • 负责人:
    KANECIA ZIMMERMAN
  • 依托单位:
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