Plus, a webinar this Thursday for your top questions
Plus, a webinar this Thursday for your top questions
Cystic Fibrosis Foundation
We are thrilled to share that the U.S. Food and Drug Administration has approved the use of Trikafta® (elexacaftor/tezacaftor/ivacaftor) for children with cystic fibrosis ages 6 to 11 who have at least one copy of the F508del mutation or one copy of certain rare mutations.

With this approval, approximately 1,500 children will be eligible for a CFTR modulator for the first time. Today’s news is a significant step forward in our mission to help all people with CF lead long, fulfilling lives, as research suggests that beginning treatment with a modulator early could help slow or even prevent the irreversible progression of cystic fibrosis.
READ THE ANNOUNCEMENT
If you’re a parent or caregiver to a child with CF, join us for a community webinar from 7-8 p.m. ET on Thursday, June 10, to have your top questions answered by experts from the Cystic Fibrosis Foundation. All those who register will receive a recording of the event.
SAVE YOUR SEAT
It is thanks to your participation in clinical trials and fundraising efforts that we have been able to reach this important milestone. Together, we will not stop until everyone has a treatment for the underlying cause of their disease.
  We will not rest until we find a cure  
Opt-out of this mailing list
Opt-out of all CFF emails