NIH-funded research U01 cooperative agreement

Using mouse models to improve treatment for idiopathic pulmonary fibrosis

Official title: Surfactant Protein C Mouse Models: A Fit For Purpose Preclinical Platform For Advancing Discovery In And Treatment Of Idiopathic Pulmonary Fibrosis

Funded at University of Pennsylvania · NIH-10754510 · Data updated 2026-11-12

This study is looking at a serious lung disease called idiopathic pulmonary fibrosis (IPF) in older adults by creating special mouse models to help us learn how certain gene changes affect the disease, with the hope of finding new treatments to help people with IPF feel better.

More Fibrosis research and trials

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionUniversity of Pennsylvania
NIH-funded
Lab location1 site (Philadelphia, United States)
Project startJanuary 1, 2021
Project endDecember 31, 2025
Funding year2024
Award (this year)$765,307
NIH project number5U01HL152970-04
Project IDNIH-10754510 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are older adults diagnosed with idiopathic pulmonary fibrosis or those with a family history of the disease.

Less likely to help

Patients with other forms of lung disease unrelated to idiopathic pulmonary fibrosis may not benefit from this research.

What this research studies

This research focuses on idiopathic pulmonary fibrosis (IPF), a serious lung disease affecting older adults, by developing advanced mouse models that mimic the disease. These models will help researchers understand how mutations in a specific gene related to lung function contribute to IPF and its progression. By studying these models, the research aims to identify new therapeutic strategies that could lead to better treatment options for patients suffering from this condition.

Why it matters

Potential benefit: If successful, this research could lead to more effective treatments for patients with idiopathic pulmonary fibrosis.

How similar studies have gone: Previous research has shown promise in using similar mouse models to advance understanding and treatment of lung diseases, indicating a potential for success in this approach.

Where this research is happening

  • University of Pennsylvania
    Philadelphia, United States
    Active

Researchers

  • Principal investigator: Beers, Michael Francis — University of Pennsylvania
  • Study coordinator: Beers, Michael Francis

Related research

Other NIH-funded projects on the same topics.

  • 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).

    NIH research Oleolive, INC. · Shreveport, United States · NIH-11550918

  • 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).

    NIH research Henry Ford Health + Michigan State University Health Sciences · East Lansing, United States · NIH-11494256

  • 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.

    NIH research University of Kansas Medical Center · Kansas City, United States · NIH-11411171

  • 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.

    NIH research Vasarya Therapeutics, INC. · Camden, United States · NIH-11382077

  • 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).

    NIH research Henry Ford Health + Michigan State University Health Sciences · East Lansing, United States · NIH-11366024

  • 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.

    NIH research University of Michigan at Ann Arbor · Ann Arbor, United States · NIH-11365030

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.