NIH-funded research U01 cooperative agreement

Targeting a specific protein to treat lung fibrosis in ferrets

Official title: Therapeutic targeting of MUC5B in a novel ferret model of idiopathic pulmonary fibrosis

Funded at University of Alabama at Birmingham · NIH-10745662 · Data updated 2026-11-12

This study is looking at how a protein called MUC5B affects idiopathic pulmonary fibrosis (IPF) using ferrets, which have lungs similar to ours, to help find new ways to treat or even reverse the disease.

More Fibrosis research and trials

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionUniversity of Alabama at Birmingham
NIH-funded
Lab location1 site (Birmingham, United States)
Project startDecember 15, 2020
Project endNovember 30, 2025
Funding year2024
Award (this year)$564,741
NIH project number5U01HL152978-04
Project IDNIH-10745662 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are individuals at risk for or diagnosed with idiopathic pulmonary fibrosis, particularly those with genetic predispositions related to MUC5B.

Less likely to help

Patients with other forms of lung disease or those not affected by idiopathic pulmonary fibrosis may not benefit from this research.

What this research studies

This research investigates the role of the MUC5B protein in idiopathic pulmonary fibrosis (IPF) using a novel ferret model. The study aims to understand how MUC5B contributes to the development of IPF and to identify potential therapeutic targets that could halt or reverse the disease. By utilizing ferrets, which have lung physiology similar to humans, researchers hope to replicate key features of human IPF and evaluate new treatment strategies. The approach includes exposing ferrets to bleomycin to induce lung fibrosis and studying the resulting changes at a molecular level.

Why it matters

Potential benefit: If successful, this research could lead to new therapies that effectively treat or manage idiopathic pulmonary fibrosis.

How similar studies have gone: While murine models have been used in similar research, this ferret model represents a novel approach that has not yet been extensively tested.

Where this research is happening

  • University of Alabama at Birmingham
    Birmingham, United States
    Active

Researchers

  • Principal investigator: Rowe, Steven Mark — University of Alabama at Birmingham
  • Study coordinator: Rowe, Steven Mark

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.