Phase 2 Interstitial Lung Disease Trial, Recruiting NCT07036523 Sponsor: Boehringer Ingelheim Condition: Interstitial Lung Disease
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Phase 2 Interstitial Lung Disease Trial, Recruiting

NCT07036523
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 of age or older at the time of signing the consent form
  • You have agreed to take part by signing and dating a consent form before the trial begins
  • You are male, or if female, you are no longer able to become pregnant — either because you have had surgery to prevent pregnancy (such as removal of the womb, fallopian tubes, or ovaries), or because you have been through menopause (no periods for 12 months without another medical reason); male participants with female partners who could become pregnant must use a condom during treatment and for a set period after their last dose
  • You have been officially diagnosed with a lung disease called IPF (Idiopathic Pulmonary Fibrosis) before the first study visit, confirmed using the most recent specialist guidelines from 2022
  • You have had a specific type of chest scan (called an HRCT) within the last 12 months showing a pattern consistent with IPF, as confirmed by a central review team
  • The scarring in your lungs covers at least 20% of your lungs, as shown on your chest scan and confirmed by a central review
  • Your lungs can hold and move at least 45% of the air expected for a healthy person of your age and size (confirmed by a breathing test)
  • Your lungs are able to transfer at least 20% of the oxygen expected for a healthy person of your age and size (confirmed by a breathing test)

Who may not be able to join:

  • You have had a sudden, serious worsening of your IPF in the 12 weeks before the first study visit or during the screening period
  • Your breathing tests show a significant blockage in your airways
  • You have had a chest or lung infection that needed treatment within the 4 weeks before the first study visit or during the screening period
  • You have significant high blood pressure in the arteries of your lungs or signs of serious right-side heart failure (confirm with trial site)
  • You have been taking IPF medications called nintedanib or pirfenidone for less than 12 weeks before the first study visit, or you are planning to start either of these medications within the first 12 weeks of the trial, or you are taking both of these medications together
  • You have serious heart or blood pressure problems, including very high blood pressure that is not controlled by medication, or a heart attack, stroke, or mini-stroke within the past 6 months, or unstable chest pain (angina) within the past 6 months
  • Your doctors estimate that another serious health condition (not IPF) means you are unlikely to live for more than 2.5 years

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: 1-800-243-0127

Australian sites

The Prince Charles Hospital, Chermside, Queensland
1800271035
Monash Health, Clayton, Victoria
1800271035
Institute for Respiratory Health, Nedlands, Western Australia
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 2
Registry
ClinicalTrials.gov
Start date
13 November 2025
Est. completion
11 March 2027

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇨🇦 Canada 🇩🇪 Germany 🇮🇹 Italy 🇯🇵 Japan 🇰🇷 South Korea 🇪🇸 Spain 🇨🇭 Switzerland 🇺🇸 United States

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

Primary endpoints

Absolute change from baseline in FVC (mL) at 12 weeks

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