The Rare Lung Disease Consortium is designed to accelerate the development and application of new knowledge about rare lung disorders, and engage the respective lung disease communities and clinical research centers for treatment trials in rare lung diseases, with the ultimate goal of developing therapies that improve the quality of life for patients by driving the process from pilot studies to FDA approval. The Administrative Core will provide leadership and oversight to the network, building on the institutional support of major clinical research centers with CTSAs and a growing network of RLD clinical care sites. The leadership is comprised of scientists with international recognition for their research on the molecular pathogenesis, diagnosis, and therapy of rare lung disorders. The directors have significant experience in the organization, implementation, and effectiveness of a rare disease clinical research network providing a bridge between clinical investigators and trainees/academic institutions, patient groups, and the general public. The goals of the Administrative Core include coordinating and facilitating communications, organizing infrastructure support, managing policies and documentation, creating and distributing educational materials, and providing fiscal administration of the consortium. Project support includes the organization of a Biostatistics Core and Radiology Core, to provide standardized and expert support to the RLD clinical research studies. The Administrative Core will produce policy and procedure manuals to organize data management between and within the projects, and streamline IRB protocol approval to facilitate multicenter and multinational clinical research studies. The RLDC will collaborate with the RDCRC and the Data Management Coordination Center to collect and transfer data seamlessly between projects. The Administrative Core will also provide guidance on web portal content, and create web content as part of our training program. The RLCN directors and PIs have partnered with patient advocates to create a RLDC Steering Committee that will guide project and program strategies, with advice and oversight of internal and external experts in translational pulmonary research. Coordinated communication, standardized protocols, and administration of multi-center clinical trial sites will create an infrastructure to support significant advances in rare lung disease research.

Public Health Relevance

The Rare Lung Disease Consortium will build a network of academic institutes, clinical! care centers, and patient advocates to create a research and training program that will make advances in the treatment of rare lung diseases. The Administrative Core will provide the leadership, communication strategies and financial administration to run the consortium smoothly, and create policies and procedures for human research protocols and data management that will provide standardized models for research across the network.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54HL127672-01
Application #
8920717
Study Section
Special Emphasis Panel (ZTR1-CI-8 (01))
Program Officer
Eu, Jerry Pc
Project Start
Project End
Budget Start
2014-09-18
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
Total Cost
$488,175
Indirect Cost
$123,025
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
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Kropski, Jonathan A; Young, Lisa R; Blackwell, Timothy S et al. (2017) Reply: The Genetic Diagnosis of Interstitial Lung Disease: A Need for an International Consensus. Am J Respir Crit Care Med 195:1539-1540
Kropski, Jonathan A; Reiss, Sara; Markin, Cheryl et al. (2017) Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in Families. Am J Respir Crit Care Med 196:1481-1484
Kugathasan, Subra; Denson, Lee A; Walters, Thomas D et al. (2017) Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study. Lancet 389:1710-1718

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