Excited to offer participation in GRAMPUS-CF to patients with cystic fibrosis worldwide. Just click on the link to join the study! https://t.co/EnAha4Gjfo @cftrust@CF_Foundation@alloonsl@CFAware
Today the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion for our fifth cystic fibrosis (CF) medicine. This is an important step towards our goal of treating all people living with CF.
Today the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion for the label expansion of our fourth cystic fibrosis (CF) medicine to include an expanded population with certain mutations. This marks an important step towards our goal of treating all people with CF.
Body composition changes and clinical outcomes in pediatric cystic fibrosis during 24 months of lumacaftor ivacaftor therapy based on real-world data | Scientific Reports https://t.co/byCtlTdKxw
🚨 New in The Lancet Respiratory Medicine
Phase 3 data on vanzacaftor–tezacaftor–deutivacaftor in #cysticfibrosis
Read open access here:
Patients aged 6–11 years https://t.co/d7R7w1hsgo
Patients aged 12 years and older https://t.co/Xl4qJtcS2C
GRAMPUS-CF aims to understand gut symptoms in people with cystic fibrosis (CF)
so that we can develop treatments. If you are a person with CF, you can help! Visit
our website for participant information, online consent and to download the app.
https://t.co/FoOUpNDK8x Thank you!
UK #CysticFibrosis community! Tell us about your thoughts on inhaled meds & interacting with your care providers post-Kaftrio in this anonymous 5-10 min research survey. Your voice matters! Please share! [https://t.co/HDX6Qjf1CY] #CF
Trikafta revolutionized treatment for Cystic Fibrosis, reaching >90% of patients variants.
But what about the remaining untreatable 10%?
We studied several poorly responsive, FDA-unapproved variants and paved a path forward for drug development.
https://t.co/cGQOqYegwe 1/7