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Advocacy Cystic Fibrosis Foundation Participates in HHS Roundtable on Drug Pricing

Yesterday, the Cystic Fibrosis Foundation met with HHS Secretary Tom Price and seven other patient advocacy groups to discuss drug pricing and the needs of the CF community. President Trump has identified drug pricing as a top priority, and this meeting was the start of a listening tour by the Secretary.

| 2 min read
Get Involved teamMATEs for a Cure: CF Foundation Hosts Largest Annual Volunteer Leadership Conference Ever

The Cystic Fibrosis Foundation took the Volunteer Leadership Conference (VLC) on the road this year and hosted the event in Dallas on April 7 and 8.

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In the Spotlight | Get Involved CF Foundation Recognizes Three CF Community Leaders at the 2017 Volunteer Leadership Conference

On April 7, the Foundation presented the AlexJena, and Dream Big Awards to leaders in the cystic fibrosis community for their dedication to the Foundation's mission of finding a cure.

| 4 min read
Research | Drug Pipeline Anti-Inflammatory Drug Shows Promising Early Results for CF

Corbus Pharmaceuticals reported promising results Thursday from an early stage clinical study of a potential anti-inflammatory drug for people with cystic fibrosis.

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Medications Positive Results from Two Phase 3 Clinical Studies of Tezacaftor (VX-661) and Ivacaftor

Two Phase 3 clinical trials of tezacaftor (VX-661) in combination with ivacaftor (Kalydeco®) showed positive results, Vertex Pharmaceuticals announced today.

| 4 min read
Health Care Reform | Advocacy | Insurance Cystic Fibrosis Foundation Joins 86 Organizations to Call on Congress to Protect Medicaid

On March 20, the Cystic Fibrosis Foundation and 86 other organizations called on Congress to protect Medicaid, a critical source of coverage for people in the cystic fibrosis community. 

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Health Care Reform | Advocacy Cystic Fibrosis Foundation Issues Statement on House Health Reform Bills

This week, House committees released legislation to repeal and replace the Affordable Care Act. The Cystic Fibrosis Foundation issued a statement consistent with our ongoing work to promote policies to help ensure that people with cystic fibrosis have access to high-quality, specialized care and adequate affordable insurance.

| 3 min read
Health Care Reform | Advocacy CF Advocates Convene on Capitol Hill for 2017 March on the Hill

As part of the Cystic Fibrosis Foundation's 11th annual March on the Hill, more than 100 advocates from 44 states met with nearly 300 elected officials or their staff to help ensure that everyone with cystic fibrosis has access to high-quality, specialized care and adequate, affordable health care.

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Clinical Trials | Researcher Resources | Cystic Fibrosis Foundation Therapeutics (CFFT) Drug Company Ends Ataluren Program for CF Nonsense Mutations

PTC Therapeutics has discontinued development of ataluren as a potential treatment for people with cystic fibrosis caused by a nonsense mutation. The Cystic Fibrosis Foundation is supporting efforts to pursue treatments for people with CF who have a nonsense, splicing or other rare mutations. 

| 3 min read