NIH-funded research R01 grant

Proteomic profile of IPF progression to help tailor treatments

Official title: Proteomic Profiling of Idiopathic Pulmonary Fibrosis Progression Trajectory

Funded at University of Michigan at Ann Arbor · NIH-11365030 · Data updated 2026-11-12

A study will look for blood protein patterns that predict how IPF lung disease 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 year2026
Award (this year)$662,677
NIH project number5R01HL169166-04
Project IDNIH-11365030 on NIH RePORTER

Who could benefit from this research

Could help

Adults diagnosed with idiopathic pulmonary fibrosis who can provide blood samples and participate in long-term follow-up.

Less likely to help

Patients with IPF for whom blood-based biomarkers do not clarify progression or who cannot participate in follow-up assessments.

What this research studies

This project uses a high-throughput blood test to measure about 3,000 proteins in people with idiopathic pulmonary fibrosis (IPF) to find markers that predict whether their lung function will worsen over a year. Researchers will test these markers in large groups from the PROFILE and Pulmonary Fibrosis Foundation cohorts and use machine learning to build a proteomic signature that forecasts FVC decline. The team will create and validate a quantitative platform to measure the chosen proteins and assess how well the signature predicts disease trajectory in future patients. If successful, the work could enable earlier and more targeted trials and treatment approaches for IPF.

Why it matters

Potential benefit: If the proteomic signature is accurate, doctors could forecast IPF progression more precisely and tailor therapies sooner.

How similar studies have gone: Previous studies have identified blood protein changes in IPF, but this project aims to create a validated predictive signature.

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

  • Adrenergic Nerves and Noradrenaline in Lung Fibrosis

    A physician-scientist-in-training at Yale seeks to build a patient-focused research program on how nerve signals and adrenaline affect lung scarring in IPF.

    NIH research Yale University · New Haven, United States · NIH-11351083

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.