NIH-funded research R01 grant

Understanding how Idiopathic Pulmonary Fibrosis changes over time

Official title: Proteomic Profiling of Idiopathic Pulmonary Fibrosis Progression Trajectory

Funded at University of Michigan at Ann Arbor · NIH-11111170 · Data updated 2026-11-12

This research aims to find markers in the blood that can help predict how Idiopathic Pulmonary Fibrosis (IPF) will progress in patients.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Michigan at Ann Arbor
NIH-funded
Lab location1 site (Ann Arbor, United States)
Project startSeptember 1, 2023
Project endMay 31, 2028
Funding year2025
Award (this year)$685,748
NIH project number5R01HL169166-03
Project IDNIH-11111170 on NIH RePORTER

Who could benefit from this research

Could help

This research is relevant to patients diagnosed with Idiopathic Pulmonary Fibrosis, especially those whose blood samples contribute to large research cohorts.

Less likely to help

Patients without Idiopathic Pulmonary Fibrosis or those not involved in providing samples for this specific research may not directly benefit from this particular study.

What this research studies

Idiopathic Pulmonary Fibrosis (IPF) is a serious lung disease where the way it progresses can be very different for each person. This makes it hard to develop new treatments because it's difficult to tell if a drug is working. Our goal is to use advanced blood tests to look at thousands of proteins in patient samples. By using powerful computer analysis, we hope to find specific protein patterns that can predict how a patient's lung function might change over a year. This could help doctors better understand each patient's disease and guide future treatment choices.

Why it matters

Potential benefit: If successful, this work could lead to better ways to predict how IPF will progress, helping doctors make more informed treatment decisions and speeding up the development of new medications.

How similar studies have gone: While proteomic platforms are emerging, the ability to accurately predict IPF progression trajectory remains largely elusive, making this a novel and important area of investigation.

Where this research is happening

  • University of Michigan at Ann Arbor
    Ann Arbor, United States
    Active

Researchers

  • Principal investigator: Oldham, Justin M — University of Michigan at Ann Arbor
  • Study coordinator: Oldham, Justin M

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.