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Revised Law Includes Designated Funding for Rare Diseases

Historic Time in Treatment of Rare Disease as Promising Drugs Reach Phase 3 Trials

Legislation to Help Speed Research for Cystic Fibrosis and Other Rare Diseases

Cystic Fibrosis Foundation Drug Development Model Spawns More Than 30 Promising Therapies

Kids from 20 States Make Case for Drug Funding and Access to Care for Fatal Disease

Legislation Would Increase Patient and Expert Participation in FDA Review of Rare Disease Treatments

Legislation Would Increase Patient and Expert Participation in FDA Review of Rare Disease Treatments

CFF-Championed Bill Eliminates Barriers to Participation in Clinical Trials for People with CF and other Rare Diseases