Phase 2 Interstitial Lung Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 40 years of age or older
- People who have been diagnosed with Idiopathic Pulmonary Fibrosis (IPF), a type of lung scarring disease
- People with IPF who are either currently taking an approved anti-scarring medication at a steady, unchanged dose, or who are not currently taking any standard treatment for IPF
- People whose lungs are still functioning at 45% or more of the expected normal level, based on a breathing test called FVC
- People whose lungs are still able to transfer oxygen into the blood at 25% or more of the expected normal level, based on a test called DLCO (confirm with trial site)
Who may not be able to join:
- People who have a different type of lung scarring disease other than IPF
- People whose chest scans show more emphysema (air trapping damage) than lung scarring
- People who are currently experiencing a sudden worsening of their IPF symptoms
- People who currently have a lower airway or lung infection that requires treatment
- People who have recently had a heart attack, unstable chest pain, or a heart procedure such as a stent or bypass surgery
- People who have heart failure
- People who have previously had an organ transplant, or for whom a lung transplant is being considered in the near future
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 1-877-240-9479
Australian sites
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
2 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
To evaluate the clinical efficacy of AZD8965 compared with placebo on the absolute change from baseline in FVC in mL at Week 24
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.