Phase 3 Interstitial Lung Disease Trial, Recruiting NCT07201922 Sponsor: Boehringer Ingelheim Condition: Interstitial Lung Disease
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Phase 3 Interstitial Lung Disease Trial, Recruiting

NCT07201922
Recruiting Phase 3 🇦🇺 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 of age or older at the time of signing the consent form.
  • You have at least one close blood relative (a parent, brother, sister, or child) who has been diagnosed with a form of pulmonary fibrosis (scarring of the lungs), including IPF, NSIP, or a genetically caused lung scarring condition.
  • A special type of CT scan (a high-resolution CT) has shown signs of early changes or abnormalities in at least a portion of one of your lungs.
  • Your lungs are able to hold and move air at a reasonably normal level (at least 80% of what would be expected for someone your age and size), based on a breathing test.
  • Your lungs are able to transfer oxygen into your blood at a reasonably normal level (at least 70% of what would be expected), based on a breathing test.
  • Additional inclusion criteria may apply (confirm with trial site).

Who may not be able to join:

  • You already have a known pulmonary fibrosis diagnosis that your doctor believes needs to be treated with approved medications.
  • A breathing test shows a certain pattern suggesting your airways may be obstructed or narrowed (confirm with trial site).
  • Your CT scan shows signs of a specific pattern of lung scarring called "usual interstitial pneumonia" (UIP) that looks probable or definite.
  • You have a medical condition known to cause lung scarring, such as a connective tissue disease (for example, rheumatoid arthritis or lupus).
  • You have previously taken or are currently taking any of these medications: nerandomilast, nintedanib, or pirfenidone.
  • Additional exclusion criteria may apply (confirm with trial site).

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 19 July 2026
Phase 3: approximately ~65% 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: 1-800-243-0127

Australian sites

Royal Prince Alfred Hospital, Camperdown, New South Wales
1800271035
Lung Research Queensland, Chermside, Queensland
1800271035
The Prince Charles Hospital, Chermside, Queensland
1800271035
The Alfred Hospital, Melbourne, Victoria
1800271035

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 3
Registry
ClinicalTrials.gov
Start date
10 February 2026
Est. completion
14 May 2029

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇪 Belgium 🇨🇦 Canada 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Time to physiologic or radiologic worsening of ILA/ILD over the whole trial

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: 19 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