Idiopathic Pulmonary Fibrosis Clinical Research Network

特发性肺纤维化临床研究网络

基本信息

批准号：
7227047
负责人：
Talmadge E King
金额：
$ 18.35万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-05-01 至 2010-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7227047
关键词：
Acute Lung Injury Address Adverse event Advisory Committees Alabama American Anatomy Antigen Presentation Appendix Area Arkansas Autoimmunity Award Azathioprine Basic Science Biological Biological Preservation Biology Biopsy Blood British Columbia Bronchoalveolar Lavage Bronchoalveolar Lavage Fluid CCL2 gene California Case-Control Studies Catchment Area Cell Communication Cells Cessation of life Chest Chronic Obstructive Airway Disease Classification Clinic Clinical Clinical Data Clinical Pathology Clinical Research Clinical Treatment Clinical Trials Clinical Trials Data Monitoring Committees Collaborations Collection Colorado Communities Condition Conduct Clinical Trials Consensus Cyclophosphamide Cysteine Protease Cytopathology Data Data Analyses Data Coordinating Center Databases Development Diagnosis Diagnostic Diffuse Disease Doctor of Medicine Dose Double-Blind Method Educational process of instructing Endopeptidases Enrollment Environment Environmental Exposure Epidemiology Etiology European Exposure to Extracellular Matrix Faculty Family Fibroblasts Fibrosis Fostering Funding Future Gene Expression Genes Genetic Goals Grant Hamman-Rich syndrome Health High Resolution Computed Tomography Histocompatibility Antigens Class II Homeostasis Hospitals Human Subject Research Image Immunity Inflammation Inpatients Institution Integrins Interferon Type II Interferon gamma 1b International Interstitial Lung Diseases Interstitial Pneumonia Iowa Journals Knowledge Label Laboratories Lead Leadership Liquid substance Location Longitudinal Studies Lung Lung Inflammation Lung Transplantation Lung diseases Lupus Macrophage Activation Malignant neoplasm of lung Measures Medical Medical center Medicine Messenger RNA Metabolism Metalloproteases Methods Michigan Modality Monitor Multicenter Studies Multicenter Trials Names New Mexico Newly Diagnosed Nonspecific Interstitial Pneumonia Numbers Observational Study Operative Surgical Procedures Oral Other Resources Outcome Pathogenesis Pathologic Pathologist Pathology Patient Care Patient Recruitments Patient Selection Patients Peptide Hydrolases Pharmacologic Substance Pharmacotherapy Phase III Clinical Trials Phenotype Physician Executives Physicians Pirfenidone Placebo Control Placebos Play Pneumonia Policies Population Population Study Prednisone Preparation Principal Investigator Procedures Process Protocols documentation Publications Pulmonary Emphysema Pulmonary Fibrosis Pulmonary Hypertension Pulmonary Pathology Pulmonary Surfactants Purpose Radiology Specialty Randomized Range Rate Recombinant Interferon-gamma Recruitment Activity Regulation Reporting Research Research Activity Research Design Research Infrastructure Research Personnel Research Project Grants Resolution Resources Review Committee Rheumatoid Arthritis Role Safety Sampling Schedule Scientist Scleroderma Severity of illness Site Site Visit Smoke Societies Source South Carolina Specimen Staging Structure of parenchyma of lung Support of Research System Teaching Materials Telephone Testing Therapeutic Intervention Therapy Clinical Trials Tissues Tobacco Tobacco smoke Training Translational Research Treatment Efficacy U-Series Cooperative Agreements United States United States National Institutes of Health Universities Vermont Voting Washington Work Wound Healing X-Ray Computed Tomography abstracting adhesion receptor base bosentan capitate bone cell motility chemokine cohort concept cost effectiveness cytokine data management day design experience fibrogenesis gene environment interaction genetic linkage analysis genetic risk factor inhibitor/antagonist interest interstitial mast cell medical schools member migration multidisciplinary mycophenolate mofetil novel therapeutics organizational structure patient oriented prevent programs pulmonary function quality assurance radiologist repository research clinical testing research facility respiratory subcutaneous success symposium tomography volunteer willingness

项目摘要

DESCRIPTION (provided by applicant): Idiopathic pulmonary fibrosis (IPF) is the most common interstitial lung disease of unknown etiology and is characterized by a relentless progression to death - only 20 to 30% of IPF patients survive 5 years or longer after their diagnosis. Conventional management of IPF has been primarily based on the concept that suppressing inflammation would prevent progression to fibrosis. Clearly, this approach has failed; there is no effective treatment currently in use. The purpose of this application is to participate in the IPF Clinical Research Network (IPF-CRN) whose goal is to evaluate new and existing approaches for the management of IPF and to disseminate the findings generated from these studies to the medical community. In support of this application, we present two protocols that address important clinical questions, test novel therapeutic approaches for IPF, and require a multicenter, academic research network for completion. Specific Aims: 1) to assemble a multidisciplinary group of clinical and basic scientists to collaborate in the design and implementation of therapeutic trials for the treatment of patients with newly diagnosed IPF, as part of the multicenter IPF Clinical Research Network; and 2) to use the clinical research infrastructure established by the UCSF Interstitial Lung Disease Center of Excellence (ILD-COE) to implement multicenter clinical trials conducted under the auspices of IPF-CRN. Protocol 1: A randomized, double-blind, placebo-controlled, multicenter trial of prednisone plus azathioprine in the treatment of IPF. Protocol 2: A randomized, double blind, placebo controlled, multicenter trial of interferon gamma-1b plus pirfenidone in the treatment of IPF. (End of Abstract)

描述（由申请人提供）：特发性肺纤维化 (IPF) 是最常见的间质性肺疾病，病因不明，其特点是不断进展至死亡 - 只有 20% 至 30% 的 IPF 患者在诊断后存活 5 年或更长时间。 IPF 的常规治疗主要基于抑制炎症可防止进展为纤维化的概念。显然，这种方法失败了。目前尚无有效的治疗方法。此应用程序的目的是参与 IPF 临床研究网络 (IPF-CRN)，其目标是评估新的和现有的 IPF 管理方法，并向医学界传播这些研究的结果。为了支持这一应用，我们提出了两个方案来解决重要的临床问题，测试 IPF 的新颖治疗方法，并需要多中心学术研究网络才能完成。具体目标： 1) 组建一个由临床和基础科学家组成的多学科小组，合作设计和实施治疗新诊断 IPF 患者的治疗试验，作为多中心 IPF 临床研究网络的一部分； 2) 利用 UCSF 间质性肺疾病卓越中心 (ILD-COE) 建立的临床研究基础设施，实施在 IPF-CRN 主持下进行的多中心临床试验。方案 1：泼尼松联合硫唑嘌呤治疗 IPF 的随机、双盲、安慰剂对照、多中心试验。方案 2：干扰素 γ-1b 加吡非尼酮治疗 IPF 的随机、双盲、安慰剂对照、多中心试验。（摘要完）