Core A: Administrative & Regulatory

项目摘要：核心A 计划的总体目标是雄心勃勃和复杂的：迭代、理性和迅速地选择一个 安全有效的联合抗逆转录病毒(ARV)非疫苗生物医学预防(NBP)候选方案 在体外、体内和临床测试中，并建立制造该候选材料的能力 临床研究。IPCP-MBP调查人员致力于局部NBP的发展 候选人和提供系统，以防止艾滋病毒的性传播。为了实现这些目标，该计划 必须由一个强大的行政和监管核心(核心A)运行。总体计划PI、项目负责人、 关键人员拥有丰富的行政和监管经验，他们成功地实现了这一点 完成这个项目。IPCP-MBP的成功将依赖于核心A提供科学、规范和 协调五大科技工程、一大科学核心、多大科技的行政领导 调查人员和组成IPCP-MBP的地点。核心A的主要目标是高效地促进 互动，为计划的财务管理提供可靠的基础设施，提供持续的 与NIH和项目官员以及科学咨询小组(SAP)的沟通 国家卫生研究院。它将为整个项目的有效领导提供重点，促进 执行委员会(EC)和指导委员会(SC)成员、项目调查员和工作人员。核心A将 还监测数据获取和共享，协调和监测材料和样品的交换 在项目和核心之间，以便研究以综合迭代的方式进展，以满足 个别项目和方案里程碑。核心A的监管方面将与和 支持参与获得IACUC、IRB、PSRC和IND批准的行政和科学人员 在项目中需要。它将确保来自探索性临床试验的数据得到适当的管理和分析 核心B和项目5的制造和测试的所有GMP和GLP要求均得到满足 有记录在案。

PROJECT SUMMARY: CORE A The Overall Program objectives are ambitious and complex: to iteratively, rationally, and expeditiously select a safe and effective combination antiretroviral (ARV) non-vaccine biomedical prevention (nBP) candidate through in vitro, in vivo, and clinical testing, and to establish the capability to manufacture this candidate for future clinical studies. The IPCP-MBP investigators are deeply committed to the development of topical nBP candidates and delivery systems to prevent the sexual transmission of HIV. To meet these goals, the Program must be run by a strong Administrative & Regulatory Core (Core A). The Overall Program PI, Project Leads, and key personnel have significant administrative and regulatory experience, which they bring to successfully complete this project. Success of this IPCP-MBP will rely on Core A to provide scientific, regulatory, and administrative leadership in coordinating the five Scientific Projects, one Scientific Core, and the multiple investigators and sites that make up this IPCP-MBP. Core A will have the primary goals of efficiently facilitating interactions, providing a reliable infrastructure for fiscal management of the Program, providing on-going communications with NIH and the Project Officer as well as the Scientific Advisory Panel (SAP) approved by NIH. It will provide focus for efficient leadership of the overall project by facilitating communication between the Executive Committee (EC) and Steering Committee (SC) members, project investigators, and staff. Core A will also monitor data acquisition and sharing, and coordinate and monitor the exchange of materials and samples between the Projects and Cores, so that the research progresses in an integrated iterative fashion to meet individual project and programmatic milestones. The regulatory aspect of Core A will coordinate with and support the administrative and scientific staff involved in gaining IACUC, IRB, PSRC, and IND approvals required in Projects. It will ensure data from the Exploratory Clinical Trial is properly managed and analyzed and that all GMP and GLP requirements for manufacture and testing in Core B and Project 5 are satisfied and documented.