Cystic Fibrosis organisations in Australia provide support and services to people with Cystic Fibrosis (CF) and their carers and families. This is complemented by a commitment to research and a quality improvement program focussing on improved clinical care for people with CF.
Every four days a baby is born in Australia with cystic fibrosis (CF) and more than one million Australians are carriers of cystic fibrosis. Cystic Fibrosis Australia (CFA) is committed to improving clinical practice and patient outcomes through its quality improvement programmes and research with the aim of extending life expectancy from 37 to 50 years by 2025.
Cystic Fibrosis is a recessive genetic condition. It primarily affects the lungs and digestive system because of a malfunction in the exocrine system, responsible for producing saliva, sweat, tears and mucus.
In addition to working for a cure, Cystic Fibrosis Australia also provides support and advocacy to improve the lives of people with cystic fibrosis. Get involved by raising awareness about CF, participating in a fundraising event or volunteering.
Cystic Fibrosis Australia has established a consistent approach to advocacy across Australia and is now a subject matter expert for government, industry and the media.
The Australian Cystic Fibrosis Research Trust (ACFRT) is managed by Cystic Fibrosis Australia (CFA). Since 1989 it has funded more than 300 projects valued at over $6,000,000.
Visit the media room to browse through number of resources including media representatives, press releases and reports.
Clinical trials are listed below.
Restore CFTR FunctionEnrolling Location: Multiple care centres across the US
RESTORE-CF: Phase 1/2 study of MRT5005 in adults with cystic fibrosis (Parts A & B) , protocol number NCT03375047 -Translate Bio RESTORE-CF MRT5005-101
This first human study is taking place at multiple care centers across the US. It will look at the safety and tolerability of different doses of the nebulized drug MRT5005 in adults with CF.
Age:
18 years and older
Mutation(s):
No mutation requirement
FEV1% Predicted:
50-90%
Number of Visits:
21
Length of Participation:
12 months
Restore CFTR FunctionCompleted with results Location: Multiple care centres across the US
Study of effectiveness and safety of elexacaftor/tezacaftor/ivacaftor in people with CF who have one copy of the F508del CFTR mutation (Vertex VX17-445-102) , protocol number NCT03525444 VX17-445-102
This study evaluated the effectiveness and safety the CFTR modulator drug VX-445 (elexacaftor) in combination with texacaftor and ivacaftor (ELX/TEZ/IVA). This triple combination drug is known as Trikafta. This study was for people with cystic fibrosis ages 12 and older with one copy of the F508del CFTR mutation and one copy of a minimal function mutation.
12 years and older
One copy F508del
40-90%
10
32 weeks
Study of VX-445 plus ivacaftor and tezacaftor in people with CF who have two copies of the F508 del CFTR mutation (Vertex VX17-445-103) , protocol number NCT03525548 VX17-445-103
This study evaluated the effectiveness and safety of the CFTR modulator drug VX-445 (elexacaftor) in combination with ivacaftor and tezacaftor. This triple combination is known as Trikafta. This study was for people with CF ages 12 and older who have two copies of the F508del CFTR mutation and were already taking tezacaftor plus ivacaftor.
Two copies of F508del
40 - 90%
7
10 weeks