Core A: Administrative and Biostatistics Core
核心 A:行政和生物统计学核心
基本信息
- 批准号:9982247
- 负责人:
- 金额:$ 11.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-08-15 至 2022-07-31
- 项目状态:已结题
- 来源:
- 关键词:AchievementAddressAnnual ReportsBasic ScienceBiometryBiostatistics CoreBudgetsCAR T cell therapyCancer CenterCellular immunotherapyClinicalClinical TrialsCommunicationDataDiseaseDoctor of PhilosophyEnsureGenesGenetic EngineeringGoalsHematologic NeoplasmsHuman ResourcesInfrastructureLeadershipLearningMonitorOperations ResearchPennsylvaniaPhysician ExecutivesProgress ReportsPublishingReportingResearchResearch PersonnelRoleSafetyScheduleScientistServicesStructureT cell therapyTestingTimeLineUniversitiesUpdateauthoritychimeric antigen receptor T cellsclinical implementationclinical research sitedata sharingdesigninnovationmedical schoolsmeetingsnoveloperationorganizational structurepharmacovigilancepreservationprogramsresponsesuccess
项目摘要
SUMMARY CORE A: ADMINISTRATIVE AND BIOSTATISTICS
The Administrative Core (Core A) will provide clinical and scientific leadership, effective communication and
fiscal and bio-statistical support to ensure the success of all Program Project activities. This proposal
seeks to build upon our track record in genetically engineered T cell therapy by enhancing the chimeric antigen
receptor T cell platform to specifically address systemic vulnerabilities that we have observed in our clinical
trials to date. Our overarching hypothesis is that novel gene editing approaches can remove the remaining
obstacles in the path of universally-available and universally-active CAR T cell therapy for hematologic
malignancy. We have brought together a cadre of exceptional investigators who have collaborated and
published together for many years. Each disease-focused project will be led by a recognized authority in the
field. The three cores that support this proposal have been critical to the success of our clinical CAR T cell
program to date and their expertise will underpin the success of this proposal. The centerpiece of each project
is an innovative clinical trial that seeks to test our major hypotheses. We are leveraging the proven
translational infrastructure, administrative staff and the centralized research organizations at the Center for
Cellular Immunotherapies at the Perelman School of Medicine to achieve our objectives. Strong institutional
commitment from the Abramson Cancer Center, Perelman School of Medicine and the University of
Pennsylvania have facilitated our scientific and translational achievements. The essential services
provided by Core A include: administrative support for all of the investigators in each project and core; fiscal
management and oversight for all components of the Program Project; and organization and communication of
all Program Project meetings and activities. The overall goal of this Core is effective and efficient leadership of
the P01. The roles of the Director, Co-investigators and administrative staff are to facilitate communication and
organizational structure while stimulating scientific and technological interactions. In order to achieve this goal,
the Core has established four objectives: (1) To oversee the safety and monitoring activities for Penn
and CHOP clinical sites; (2) To provide statistical support for clinical trials, projects and cores and implement
plans to promote data sharing; (3) To coordinate the interactions among clinicians and scientists in projects
and cores, internal and external advisory boards, and NCI personnel regarding effective implementation of
proposed objective; (4) To provide budgetary services such as tracking expenses and providing investigator's
monthly reports.
核心摘要 A:管理和生物统计学
行政核心(核心 A)将提供临床和科学领导、有效的沟通和
财政和生物统计支持,以确保所有计划项目活动的成功。这个提议
寻求通过增强嵌合抗原来巩固我们在基因工程 T 细胞疗法方面的记录
受体 T 细胞平台,专门解决我们在临床中观察到的系统漏洞
迄今为止的试验。我们的首要假设是,新的基因编辑方法可以消除剩余的基因
普遍可用且普遍有效的血液学 CAR T 细胞治疗之路上的障碍
恶性肿瘤。我们聚集了一批杰出的调查人员,他们通力合作,
共同出版多年。每个以疾病为重点的项目都将由该领域公认的权威领导
场地。支持这一提议的三个核心对于我们临床 CAR T 细胞的成功至关重要
迄今为止的计划和他们的专业知识将支撑该提案的成功。每个项目的核心
是一项创新的临床试验,旨在检验我们的主要假设。我们正在利用经过验证的
中心的转化基础设施、行政人员和集中研究组织
佩雷尔曼医学院的细胞免疫疗法可实现我们的目标。制度性强
艾布拉姆森癌症中心、佩雷尔曼医学院和大学的承诺
宾夕法尼亚州促进了我们的科学和转化成就。基本服务
核心 A 提供的服务包括: 为每个项目和核心的所有研究人员提供行政支持;财
管理和监督计划项目的所有组成部分;以及组织和沟通
所有计划项目会议和活动。该核心的总体目标是有效和高效地领导
P01。主任、联合研究者和行政人员的作用是促进沟通和
组织结构,同时刺激科技互动。为了实现这一目标,
核心确立了四个目标: (1) 监督宾夕法尼亚大学的安全和监测活动
和 CHOP 临床中心; (二)为临床试验、项目、核心提供统计支持并实施
计划促进数据共享; (3) 协调项目中临床医生和科学家之间的互动
和核心、内部和外部顾问委员会以及 NCI 人员关于有效实施
拟议目标; (4) 提供预算服务,例如跟踪费用和提供研究者的信息
月度报告。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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CARL H. JUNE其他文献
CARL H. JUNE的其他文献
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{{ truncateString('CARL H. JUNE', 18)}}的其他基金
Enhancing Chimeric Antigen Receptor T Cell Therapies for HematologicMalignancies: Beyond CART 19
增强嵌合抗原受体 T 细胞治疗血液恶性肿瘤:超越 CART 19
- 批准号:
10713199 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Project 2: Towards a safe and effective AML treatment strategy using anti-CD33 CAR T cells in combination with CAR-resistant hematopoietic stem cells
项目2:利用抗CD33 CAR T细胞联合CAR耐药造血干细胞,制定安全有效的AML治疗策略
- 批准号:
10245064 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Core A: Administrative and Biostatistics Core
核心 A:行政和生物统计学核心
- 批准号:
10245066 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Project 2: Towards a safe and effective AML treatment strategy using anti-CD33 CAR T cells in combination with CAR-resistant hematopoietic stem cells
项目2:利用抗CD33 CAR T细胞联合CAR耐药造血干细胞,制定安全有效的AML治疗策略
- 批准号:
9982244 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Enhancing Chimeric Antigen Receptor T Cell Therapies for Hematologic Malignancies: Beyond CART 19
增强嵌合抗原受体 T 细胞治疗血液恶性肿瘤:超越 CART 19
- 批准号:
9280418 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Enhancing Chimeric Antigen Receptor T Cell Therapies for Hematologic Malignancies: Beyond CART 19
增强嵌合抗原受体 T 细胞治疗血液恶性肿瘤:超越 CART 19
- 批准号:
10245062 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
Enhancing Chimeric Antigen Receptor T Cell Therapies for Hematologic Malignancies: Beyond CART 19
增强嵌合抗原受体 T 细胞治疗血液恶性肿瘤:超越 CART 19
- 批准号:
9982239 - 财政年份:2017
- 资助金额:
$ 11.2万 - 项目类别:
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