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AIDS-ASSOCIATED MALIGNANCIES CLINICAL TRIALS MEMBER

AIDS-ASSOCIATED MALIGNANCIES CLINICAL TRIALS MEMBER
艾滋病相关恶性肿瘤临床试验成员
批准号:
2114016
负责人:
JAMIE H VON ROENN
金额:
$17.96万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-09-30 至 1999-07-31

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中文摘要
翻译
这项建议的长期目标是提高 人类免疫缺陷病毒相关恶性肿瘤患者的生命和生存 开发创新的、病机驱动的治疗策略和 对这些肿瘤的生物学有深入的了解。要做到这一点 目标,我们目前的目标是成为临床试验的成员 艾滋病相关恶性肿瘤联合会(RFA联合会)。这项建议 提出一个由四个机构及其附属机构组成的联盟,申请 作为一个单一的临床试验成员。组成这四个机构的 我们的联盟,西北大学,华盛顿大学,约翰斯 霍普金斯肿瘤学中心和拉什医学院/伊利诺伊州共济会 医院,每个医院都有临床或基础科学方面的专业知识 为RFA联盟的使命做出贡献。 作为艾滋病相关恶性肿瘤协会的临床试验成员, 我们将在组织结构内开展活动 由财团建立。我们将全面参与规划。 以及开展联合体临床试验和研究活动。我们 将与财团充分合作,确保高效 通信,遵守联邦授权的高标准 监管要求、患者登记、出版物监督、 肿瘤反应的评估,以及生物统计学的协调 和数据收集。参加RFA协会的临床试验 将是我们的最高优先事项,并将作为 所有艾滋病相关患者的第一阶段和第二阶段临床试验 我们医院对恶性肿瘤进行了评估。
英文摘要
The long term objective of this proposal is to improve the quality of life and survival of patients with HIV-related malignancies through the development of innovative, pathogenesis driven therapeutic strategies and to gain insights into the biology of these tumors. To accomplish this aim, our immediate goal is to become a clinical trials member of the AIDS-Related Malignancies Consortium (RFA Consortium). This proposal presents a Consortium of four institutions and their affiliates, applying as a single clinical trials member. The four institutions which compose our Consortium, Northwestern University, Washington University, Johns Hopkins Oncology Center and Rush Medical College/Illinois Masonic Hospital, each have clinical or basic science expertise which will contribute to the mission of the RFA Consortium. As a clinical trials member of the AIDS-Related Malignancies Consortium, we will conduct our activities within the organizational structure established by the Consortium. We will participate fully in the planning and conduct of Consortium clinical trials and research activities. We will cooperate fully with the Consortium to ensure efficient communication, high standards of compliance with federally mandated regulatory requirements, patient registration, oversight of publications, evaluation of tumor response, as well as coordination of biostatistics and data collection. Participation in the RFA Consortium clinical trials will be our highest priority and will serve as the primary venue for Phase I and ll clinical trials for all patients with AIDS-related malignancies evaluated at our hospitals.
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