Quarterly Newsletter of the NIH Rare Diseases Clinical Research Network
December 2010

www.RareDiseasesNetwork.org

In This Issue

Introducing Spotlight on Rare Diseases

The NIH Rare Diseases Clinical Research Network (RDCRN) Doubles in Size

Message from Alan Percy, RDCRN Steering Committee Chair

About Spotlight

Current Issue of Spotlight

Network News and Events

World Rare Disease Day
February 28, 2011
rarediseaseday.us

7th Annual World Symposium, Research for Lysosomal Diseases
February 16-18, 2011

5th International Dystonia Symposium
Barcelona, Spain
October 20-22 2011

Featured Event:

2nd Annual Conference on Clinical Research for Rare Diseases (CCRRD) >> More

Rare Diseases Headlines:

President Signs "Improving Access to Clinical Trials Act" into law
>> More

CTSA Consortium to Enhance Support of Rare Diseases Research
>> More

IOM Releases Report on Accelerating Rare Diseases Research
>> More

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IOM Report to Accelerate Rare Diseases Research

The estimated 7000 rare diseases collectively affect 25-30 million of Americans of all ages. Many are life threatening or fatal. Because each rare disease affects a relatively small population, it can be challenging to develop drugs and medical devices to prevent, diagnose, and treat these conditions. To help in accelerating rare diseases research and product development, the NIH, the ORDR, and the FDA asked the IOM (Institute of Medicine) to examine the opportunities for, and obstacles in developing drugs and medical devices for treating rare diseases.

The report, released on October 4, 2010, provides a valuable guide for policymakers. It sets forth the elements of an integrated national strategy to promote rare diseases research and product development. The Office of Rare Diseases Research received accolades for the pivotal role it has played in promoting and developing the current infrastructure. Among other recommendations, the IOM calls for NIH to work with industry, academia, and voluntary organizations to develop a comprehensive system of shared resources for discovery research on rare diseases and to facilitate communication and cooperation for such research.

In addition, the IOM report calls for the Secretary of the Department of Health and Human Services to establish a national task force on accelerating rare diseases research and product development. Overall, the effort and investment needed to move further toward a collaborative, coordinated, open, and sustained approach to rare diseases will be substantial, but not making the investment will also be costly. The potential benefits justify a renewed commitment to accelerating rare diseases research and product development.

The full report is available for online reading:  http://books.nap.edu/openbook.php?record_id=12953

The report in book format can be purchased for $60: http://www.iom.edu/Reports/2010/Rare-Diseases-and-Orphan-Products-Accelerating-Research-and-Development.aspx