News

News and Press Releases
About the CF Foundation | Public Policy Statement from the Cystic Fibrosis Foundation on the House Energy and Commerce Committee’s Health Subcommittee Approval of the EXPERRT Act

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

| 5 min read
About the CF Foundation | Public Policy | Drug Pipeline Statement from the Cystic Fibrosis Foundation on Senate HELP Committee’s Approval of the EXPERRT Act

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

| 3 min read
About the CF Foundation | Advocacy | Public Policy Teens Lobby Congress to Raise Awareness of Cystic Fibrosis

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

| 2 min read
About the CF Foundation | Public Policy | Clinical Trials Improving Access to Clinical Trials Act Passes U.S. House -- Heads to President for Signature

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

| 4 min read
About the CF Foundation | Public Policy | Clinical Trials Improving Access to Clinical Trials Act Passes U.S. Senate in Victory for CF Advocates

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

| 3 min read
About the CF Foundation | Public Policy | Research NIH Director Francis Collins and CF Foundation to Brief U.S. Senate on Advancing Disease Research

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

| 3 min read
About the CF Foundation | Public Policy | Clinical Trials More than 100 Organizations Support Bill to Boost Participation in Clinical Trials for Rare Diseases

Legislation Would Remove Financial Penalties for Participating in Research Studies

| 2 min read
About the CF Foundation | Public Policy | Clinical Trials Senate Introduces Bill to Boost Participation in Clinical Trials for Rare Diseases

Bill Would Remove Financial Penalties for Participating in Research Studies

| 4 min read