NORD is pleased to announce a cooperative project with the FDA to fill the unmet need of a generalized, standard approach to natural history study development across rare diseases. Working with disease patient groups and the FDA, NORD will develop natural history studies for twenty rare diseases.
Together, we will develop a registry toolkit containing best-practice tools and templates that will aid future organizations to initiate and conduct natural history studies that are designed to support drug development programs. Additionally, we will build upon previous efforts to develop common data elements, questions and ontologies for rare diseases to provide a generalized baseline for future efforts. Each study will be sponsored by the disease patient group, will include the common data elements created as part of this project, and will include disease-specific research.
We invite proposals from disease patient groups to join this project. From the applicants, we will conduct a selection process using the review criteria below to find the twenty proposals that best fulfill the goals of the project.
For more information, read the official announcement.
Twenty rare disease patient groups have been chosen to develop natural history studies with the assistance of the National Organization for Rare Disorders (NORD) supported in part by a cooperative agreement with the U.S. Food and Drug Administration (FDA). Read the full announcement here.
Hereditary Neuropathy Foundation
Organic Acidemia Association
XLH Network, Inc.
CCHS Family Network
Pitt Hopkins Research Foundation
The OMSLife Foundation
Platelet Disorder Support Association
Global Foundation for Peroxisomal Disorders
APS Type 1 Foundation
Scleroderma Research Foundation
Desmoid Tumor Research Foundation
International Pemphigus & Pemphigoid
The Morgan Leary Vaughan Fund
Adult Polyglucosan Body Disease (APBD) Research
Bridge the Gap-SYNGAP Education and Research Foundation
United Leukodystrophy Foundation
AMENSupport (American Multiple Endocrine Neoplasia Support)
Worldwide Syringomyelia & Chiari Task Force.