Cystic fibrosis ( Cystic fibrosis )

Cystic fibrosis

Cystic fibrosis's picture

Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide).

Cystic fibrosis press release, blog etc

07/05/2018 - 04:50 CF Teen Advocates Visit Capitol Hill for 10th Annual Teen Advocacy Day
06/19/2018 - 21:14 Choate Construction Makes Corporate Impact Through 9th Annual Cars & Q for the Cause Fundraiser
06/07/2018 - 09:55 Phase 2 Study Shows Promising Results for Potential Mucus Clearance Drug
05/31/2018 - 13:11 President Trump Signs Right to Try Legislation Into Law
05/09/2018 - 11:20 Cystic Fibrosis Foundation Responds to ICER Review of CFTR Modulators
05/01/2018 - 11:36 CF Foundation Awards Icagen Up to $11 Million for Nonsense Mutation Research
04/16/2018 - 18:04 Champion Runner Meb Keflezighi Teams Up with Lee University to Raise Over $1 Million in the Fight Against Cystic Fibrosis
04/13/2018 - 07:34 CF Foundation Hosts Congressional Briefing on Protecting People With CF and Other Pre-Existing Conditions
04/05/2018 - 15:43 CF Foundation Opposes Right to Try Legislation
04/03/2018 - 14:01 4 Outstanding CF Community Leaders Honored at the 2018 VLC
03/29/2018 - 11:47 CF Foundation Hosts 15th Annual Volunteer Leadership Conference
03/28/2018 - 05:56 CF Foundation Welcomes New National Advocacy Chairs
03/19/2018 - 12:33 In D.C. and Nationwide, CF Advocates Lobby Congress During 2018 March on the Hill
03/01/2018 - 09:43 Positive Early Stage Study Results Announced for Next-Generation Modulator
02/12/2018 - 18:57 FDA Approves New CFTR Modulator Treatment for Cystic Fibrosis
01/31/2018 - 15:58 Next Stage of Triple Combination CFTR Modulator Development Announced
01/30/2018 - 05:12 CF Foundation Awards Up to $25 Million for the Development of a Novel Drug to Reduce Inflammation in CF
01/11/2018 - 08:27 The Cystic Fibrosis Foundation has awarded Icagen Inc. up to $11 million for a multi-year drug discovery program to identify and develop treatments for people with cystic fibrosis who have