Phase 2 Interstitial Lung Disease Trial, Recruiting NCT07194382 Sponsor: Avalyn Pharma Inc. Condition: Interstitial Lung Disease
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Phase 2 Interstitial Lung Disease Trial, Recruiting

NCT07194382
Recruiting Phase 2 🇦🇺 Australian site

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:

  • You are 40 years old or older at the time of signing the consent form
  • You have been diagnosed with idiopathic pulmonary fibrosis (IPF) — a condition where the lungs become scarred over time — within the last 5 years, according to recognised international guidelines
  • Your diagnosis was confirmed through a specific type of lung scan (a high-resolution CT scan) and, if you had one, a surgical lung tissue sample
  • You are in a stable condition and considered suitable to take part, based on your medical history, a physical check-up, and standard tests including blood tests and a heart trace (ECG)
  • Your lungs can hold at least 45% of the air they normally should (confirmed by a breathing test)
  • Your lungs' ability to transfer oxygen into the blood falls within a specific range — between 30% and 80% of what is considered normal (confirmed by a breathing test)
  • If you are able to have children (male or female), you must be willing to use highly effective contraception for at least 90 days after your last dose of the study drug

Who may not be able to join:

  • You are currently taking, or have taken within the last 3 months, the IPF medications nintedanib or pirfenidone by mouth — or you have previously taken both of these medications together
  • A specific breathing test result (measuring how well air flows out of your lungs) shows a certain ratio that may indicate a different lung condition (confirm with trial site)
  • You have a history of serious heart disease, significant bleeding problems, or significant liver or kidney disease (confirm with trial site for exact definitions)
  • You have a history of a bowel condition called diverticular disease, or you have had abdominal surgery within the 4 weeks before the screening visit
  • You have had cancer in the past 5 years (some exceptions may apply — confirm with trial site)
  • You have smoked within the past 3 months, are unwilling to stop smoking during the study, or currently use illegal or misused drugs
  • You are currently pregnant or breastfeeding
  • You have taken part in another clinical trial or used any experimental drug (including for IPF) within the past 30 days before screening

Please note: this is not a complete list — additional eligibility criteria may apply.


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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 206-707-0340

Australian sites

Nepean Lung and Sleep, Kingswood, New South Wales

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

Status
Recruiting
Phase
Phase 2
Sponsor
Avalyn Pharma Inc.
Registry
ClinicalTrials.gov
Start date
10 March 2026
Est. completion
1 December 2026

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Change from baseline in the morning pre-dose forced vital capacity at Week 12

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov