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.
Phase 2 study of CTX-4430 in people with CF (EMPIRE)
, protocol number Celtaxsys CTX-4430
This study is taking place at multiple care centers across the U.S. It will look at the safety and effectiveness of the anti-inflammatory drug CTX-4430 and will use a placebo control.
18 Years to 30 Years
No Mutation Requirements
50% or greater
Number of Visits:
Length of Participation:
Anti-InfectiveCompleted with results
Persistent Methicillin Resistant Staphylococcus Aureus (MRSA) Growth in Respiratory Culture
, protocol number NCT01594827 DASENB10AO, PMEP11K1, JENNIN16K0
This study will look at the safety and effectiveness of a 28-day course of vancomycin for inhalation in getting rid of the bacteria, Methicillan Resistant Staphylococcus Aureus (MRSA) from the respiratory tract of people with CF and persistent MRSA infection.
12 Years and Older
No Mutation Requirement
30% or greater
ObservationalClosed to enrollment
STOP: Standardised Treatment of Pulmonary Exacerbations Pilot Study
, protocol number FLUME13A1
This study took place at multiple care centres across the US. The goal of the study was to better understand current treatment practices for pulmonary exacerbations and whether the CF Registry can be used for this type of study.
No FEV1 Limit
IGNITE: Safety and effectiveness of gallium nitrate in adults with cystic fibrosis
, protocol number GALLIUM-IP-13
This study is taking place at multiple care centers across the US. It will look at the safety and effectiveness of IV gallium nitrate in adults with cystic fibrosis who are chronically infected with Pseudomonas aeruginosa.
18 Years and Older
25% or greater
ObservationalCompleted with results
GOAL e2 Lung Clearance Index study in children who have a CFTR gating mutation
, protocol number NCT01521338 GOAL-OB-11 Cohort 4
This study evaluated lung function in young children with CF before and after taking ivacaftor. This study was for children ages 3 to 5 years old who have at least one CFTR gating mutation.
3 Years to 5 Years
One Copy F508del or No Copies F508del
GOAL-e2 Expansion Study
, protocol number GOAL-OB-11 Expansion
This is a prospective, multi-centre observational study. This study will look at samples from people with cystic fibrosis who have the R117H and other non-G551D gating CFTR mutations, many of whom are expected to be prescribed ivacaftor during the course of the study. This study is for ages 6 and above.
6 Years and Older
One Copy F508del of No Copies F506del
PALS: Aztreonam Inhalation Solution (AZLI) Safety Study in Children with CF and Chronic Pseudomonas Aeruginosa
, protocol number Gilead GS_US_205-0160
This open-label study looked at the safety of Aztreonam Inhalation Solution (Cayston®) given three times daily for three 28-day on/28-day off cycles in children with cystic fibrosis and chronic Pseudomonas aueruginosa (PA) infection in the lower airways.
Less than 12 Years
Phase 4 study to monitor the susceptibility of Pseudomonas aeruginosa to aztreonam in people with CF
, protocol number Gilead GS-US-205-0128
This 5-year study took place at multiple care centres across the US. It investigated the susceptibility of Pseudomonas aeruginosa isolates to the anti-infective drug aztreonam.
1 Year and Older
Less than 90%
Anti-InflammatoryClosed to enrollment
Phase 2 study of GS-5745 in adults with CF
, protocol number Gilead GS-US-404-1808
This study is taking place at multiple care centers across the U.S. It will look at the effectiveness of the anti-inflammatory drug GS-5745 and will use a placebo control.
40 to 80%
Phase 2 study of JBT-101 in people with CF
, protocol number Corbus JBT101-CF-001
This study is taking place at multiple centres across the U.S. It will look at the safety and effectiveness of the anti-inflammatory drug JBT-101, as well as how the body processes the drug, in adults with CF.
18 - 65 years
No mutation requirement
40% or greater