Condition
Pulmonary Fibrosis clinical trials and research
As of November 12, 2026, Find a Trial lists 22 Pulmonary Fibrosis clinical trials that are recruiting, at sites in 11 countries (most in United States (9), China (4), Canada (2)). By phase: Phase 2 (3), Phase 1 (2), Phase 1/2 (1). The most active sponsors are Massachusetts General Hospital (3), Peking Union Medical College Hospital (2). There are also 174 NIH-funded research projects on Pulmonary Fibrosis, with $97.8 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 22Clinical trials
- 174NIH research projects
- 11Countries
Newest Pulmonary Fibrosis clinical trials
All recruiting trials (22)
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AccuPulmo CT Portal for Detecting Pulmonary Fibrosis on Chest CT
This study tests how well the AccuPulmo CT Portal can identify pulmonary fibrosis on existing chest CT scans from adults at Taichung Veterans General Hospital.
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Advanced imaging to see how immunosuppression affects lung fibrosis activity
This trial will test whether immunosuppression changes PET and MRI measurements of active collagen deposition and tissue injury in people with non‑IPF interstitial lung disease who are starting treatment.
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68Ga-NI-FAPI-04 PET/CT imaging to detect fibroblast activation in cancer, fibrotic, and heart diseases
This test will see if an injected PET tracer called 68Ga-NI-FAPI-04 can better show fibroblast activation in people with tumors, pulmonary fibrosis, certain autoimmune vascular diseases, hypertrophic cardiomyopathy, or other cardiovascular conditions.
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Home monitoring for patients with pulmonary fibrosis
This study tests if using home monitoring and video calls can help people with pulmonary fibrosis manage their condition as well as or better than regular clinic visits.
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Understanding genetic and environmental factors in pulmonary fibrosis
This study looks at how genes and environmental factors affect pulmonary fibrosis to help understand the disease better for people who have it.
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Identifying biomarkers for progressive pulmonary fibrosis in lung disease patients
This study is trying to find early signs that can help predict if adults with certain lung diseases will develop progressive pulmonary fibrosis over the next five years.
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Routine versus on-demand ECMO during lung transplant
This trial tests whether using ECMO routinely during lung transplant or only when needed leads to fewer complications for people having a lung transplant.
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Advanced Imaging for Pulmonary Fibrosis
This study is testing a new imaging technique to see if it can help doctors better understand and treat people with pulmonary fibrosis.
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Using breath analysis to identify multiple lung diseases
This study is testing if analyzing breath samples can help identify different lung diseases like lung cancer and COPD in a large group of 10,000 people.
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Using cryobiopsy to diagnose progressive pulmonary fibrosis
This study is testing a new lung biopsy method called cryobiopsy to see if it can diagnose progressive pulmonary fibrosis better and safer than the traditional method.
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Evaluating FAP as a biomarker for fibrotic lung diseases
This study is testing if a protein called FAP can help doctors understand and track fibrotic lung diseases like idiopathic pulmonary fibrosis by looking at its levels in different samples and using special scans before and after treatments.
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Predicting worsening of pulmonary fibrosis using AI from CT scans
This study is testing if using AI to analyze CT scans can help predict which patients with pulmonary fibrosis are likely to get worse over time.
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Digital self-management package for people with interstitial lung disease
This study is testing a new smartphone app designed to help people with interstitial lung disease manage their health better and feel improved overall compared to standard care.
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Biobank for interstitial lung diseases
This study is setting up a collection of health information and samples from patients with interstitial lung diseases to help researchers learn more about the condition and find better treatments.
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Registry for individuals affected by pulmonary fibrosis
This study invites people with pulmonary fibrosis, along with their caregivers and family members, to share their experiences through online surveys to help researchers understand the condition better and possibly reach out for future studies.
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Comparing two imaging methods for diagnosing pulmonary fibrosis
This study is testing if a new imaging method called 68Ga-FAPI PET/CT can better diagnose and monitor treatment for people with pulmonary fibrosis compared to the standard method, 18F-FDG PET/CT.
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Non-drug therapy for controlling cough in patients with lung disease
This study is testing a new non-drug therapy to help adults with interstitial lung disease and a long-lasting cough feel better when combined with pulmonary rehabilitation.
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Evaluating a new imaging probe for lung conditions
This study is testing a new imaging tool to see if it can safely help detect lung problems like fibrosis and cancer in healthy people and patients.
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European database and biobank for childhood interstitial lung diseases
This study is creating a database and biobank to collect information and samples from children with interstitial lung diseases across Europe to improve their treatment and understanding of these conditions.
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Using lung tissues to study pulmonary fibrosis
This study looks at lung tissues from patients with pulmonary fibrosis to see what changes happen in the lungs and how it might help find new treatments for the disease.
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Exploring genetic traits in pulmonary fibrosis
This study is trying to find out if certain genes affect how idiopathic pulmonary fibrosis develops and how it impacts lung healing in patients.
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Exploring genetic factors in lung disease development
This study is trying to find out how certain genes might play a role in lung diseases like cystic fibrosis and asthma by looking at lung cells from both patients and healthy people.
NIH-funded research (newest 40 of 174)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Molecular clues to progressive lung scarring
Researchers are studying how lung tissue becomes progressively scarred, focusing on cell signals and receptors that may drive fibrosis in people with lung disease.
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Alveolar Cell Dysfunction in Pulmonary Fibrosis: Using SFTPC Mutations to Find New Targets
This grant explores how rare SFTPC mutations in alveolar cells may drive IPF and seeks new molecular targets to improve treatment.
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Iron and scar-forming cells in the lungs (IPF)
Researchers are exploring how iron in the lungs may drive the scarring seen in idiopathic pulmonary fibrosis and whether this could lead to new therapies.
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Repurposing Pyrvinium as an Inhaled Therapy for Idiopathic Pulmonary Fibrosis
A patient-friendly look at a project trying to use an existing drug, pyrvinium, as an inhaled treatment option for idiopathic pulmonary fibrosis (IPF).
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Screening new compounds to reverse gene signatures in IPF lungs
A researcher hopes to find compounds that reverse harmful gene changes in the lungs of people with idiopathic pulmonary fibrosis (IPF).
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Role of lactate transporters in lung scarring
Aims to see if blocking lactate transporters can slow or stop scar-forming cells from thickening the lungs in people with fibrotic lung disease.
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Formyl peptide receptor links inflammation to lung disease in rheumatoid arthritis
This grant looks at how a receptor on immune cells may drive lung inflammation in people with rheumatoid arthritis and related conditions.
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p53 acetylation and alveolar stem cell aging in progressive lung fibrosis
Scientists are studying how changes to a cancer-related protein, p53, affect aging lung cells and contribute to a scary lung disease called IPF.
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Targeted nanoparticle therapy for lung fibrosis
A researcher team is testing inhaled nanoparticles that deliver medicine directly to the lungs to slow or stop scarring in people with pulmonary fibrosis.
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Understanding how tobacco smoke changes lung fibroblasts in pulmonary fibrosis
A study exploring how cigarette smoke affects lung cells to drive fibrosis, with a focus on a protein called PRMT5 and potential ways to slow disease progression.
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Lung cell transplantation for drug-induced lung scarring in cancer patients
A new approach tests transplanting lung cells to repair scarring caused by cancer drugs in people with cancer.
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Unraveling IPF subtypes to guide prognosis and therapy
This grant aims to identify different IPF subtypes in the lung to improve how we predict outcomes and tailor treatments for people with IPF.
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Understanding how early changes in lungs lead to progressive fibrotic disease
This grant studies the cells and genes involved in starting and advancing pulmonary fibrosis to uncover why some people progress to severe disease.
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Thromboxane Receptor: a new target to reduce radiation lung scarring
Aims to see if blocking a specific receptor in the lungs can reduce scarring after chest radiation in patients.
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Proteomic clues for early and late lung fibrosis
Researchers are studying protein markers in the lungs to understand how pulmonary fibrosis starts and progresses, with the aim of helping people at risk for the disease.
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Epac1 and lung scarring in idiopathic pulmonary fibrosis
Looks at whether blocking a protein called Epac1 can reduce lung scarring in people with idiopathic pulmonary fibrosis.
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Support-T: a mobile tool to help people with progressive pulmonary fibrosis and their caregivers get palliative care and planning
A mobile app called SUPPORT-T helps people with progressive pulmonary fibrosis and their caregivers access palliative care and plan for the future.
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Alveolar immune and lung cell lipid metabolism in fibrosis
A physician-scientist at UCLA is pursuing a five-year plan to understand how lipid metabolism in lung cells contributes to idiopathic pulmonary fibrosis and to build translational research using patient samples.
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Defining how early pulmonary fibrosis develops at the molecular level
Researchers are studying early stages of pulmonary fibrosis at the molecule-by-molecule level to understand how the disease starts and progresses in people.
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Functional genomic insights into epithelial dysfunction in pulmonary fibrosis
Researchers are studying people at risk for familial pulmonary fibrosis to understand how early cellular changes in the lungs develop into full disease.
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Understanding and preventing early lung fibrosis in at-risk people
A program to uncover the early clues and biology that lead to lung fibrosis and to develop ways to prevent it before symptoms start.
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Cell competition in lung fibrosis and ARDS
A Mayo Clinic team is studying how lung cells compete and repair after injury in people with severe lung diseases like IPF, ARDS, and after viral infections, to find ways to improve recovery.
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Targeting an amino acid transporter to fight lung scarring
A researcher is studying whether blocking a specific transporter (SLC7A5) in lung cells can slow or stop the scarring process seen in idiopathic pulmonary fibrosis.
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How mechanical forces affect lung scarring and metabolism in IPF
A researcher at a major university is studying how the stiffness of lung tissue and specific cellular sensors may drive metabolism changes that worsen idiopathic pulmonary fibrosis in patients.
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Novel antibody therapy to treat idiopathic pulmonary fibrosis
A small business gig is developing a targeted antibody drug (VSR-H5) to treat idiopathic pulmonary fibrosis in patients, aiming for better safety and effectiveness than current medicines.
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IgA antibodies to oxidation-related targets in lung fibrosis
This NIH grant explores how certain IgA antibodies against damaged lung components relate to idiopathic pulmonary fibrosis and what that means for future therapies.
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Predicting Post-Covid Lung Scarring with Easy-to-Understand Deep Learning and Key Biomarkers
Aims to use explainable artificial intelligence and biomarker data from multiple hospitals to predict which patients will develop long-term lung scarring after COVID-19.
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Advanced Imaging to Predict Progressive Lung Fibrosis in ILD
This grant tests imaging tools to identify people with non-IPF interstitial lung disease who will develop progressive fibrotic lung disease, so doctors can tailor treatment early.
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Collagen oxidation and cell signals in aging-related lung fibrosis
A patient-facing study exploring how aging-related changes in collagen and cell signaling contribute to scarring in the lungs of people with a condition like idiopathic pulmonary fibrosis (IPF).
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Desmoplakin’s Role in Lung Fibrosis in HD AT2 Cells
A study in adult human lung cells aims to understand how a genetic change in desmoplakin may contribute to lung fibrosis.
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Targeting WNT7A Signaling to Improve Lung Repair in Pulmonary Fibrosis
Aims to test whether blocking WNT7A signaling can help the lungs repair themselves and reduce scarring in people with a serious lung disease.
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Understanding how MUC5B gene control affects lung scarring (IPF)
This grant explores how changes in gene regulation lead to high MUC5B levels and lung scarring in IPF, with potential implications for patients living with this disease.
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Using targeted PET imaging and new treatment to predict and treat radiation-induced lung scarring
Aims to use a special PET imaging button to see a specific protein (αvβ6) in the lungs after radiation and test a new drug to prevent or treat the scarring called RIPF.
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Intracellular Collagen Sensing in Lung Fibrosis
Researchers are studying how lung cells detect and clear collagen to find new ways to reverse fibrosis in IPF.
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Optical imaging biomarker to predict lung disease outcomes in IPF
A new imaging test using tiny endobronchial optics could help predict how IPF will progress and who might need a transplant.
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Understanding why some lung repairs go wrong in pulmonary fibrosis
This NIH grant looks at why the lungs sometimes repair damage poorly after injury, with a focus on people who have or are at risk for pulmonary fibrosis.
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Repurposing Vonoprazan as an inhaled therapy for IPF
A high-profile NIH grant is testing whether an existing drug, vonoprazan, can be inhaled to slow or reverse lung fibrosis in people with idiopathic pulmonary fibrosis (IPF).
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Alveolar Cell Dysfunction in Pulmonary Fibrosis: Using SFTPC Mutations to Find New Treatments
A study focused on a specific lung cell defect linked to a common scarring lung disease (IPF) to uncover new targets for therapy.
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Proteomic profile of IPF progression to help tailor treatments
A study will look for blood protein patterns that predict how IPF lung disease will progress in patients.
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Understanding how blood vessel signals affect post-flu and post-coronavirus lung scarring
This NIH grant looks at how a specific blood vessel signal (S1PR1) in the lungs might prevent scarring after severe viral lung infections like flu or COVID-19.
Related topics
Quick answers
How many Pulmonary Fibrosis clinical trials are recruiting right now?
22, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 11 countries. The most sites are in United States (9 trials), China (4 trials), Canada (2 trials), Netherlands (2 trials), Belgium (1 trial). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 2: 3, Phase 1: 2, Phase 1/2: 1. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.