NIH-funded research R01 grant

Unraveling IPF subtypes to guide prognosis and therapy

Official title: Unraveling idiopathic pulmonary fibrosis endophenotypes; a lung-centric approach to prognostic and therapeutic biomarker validation

Funded at University of Kansas Medical Center · NIH-11411171 · Data updated 2026-11-12

This grant aims to identify different IPF subtypes in the lung to improve how we predict outcomes and tailor treatments for people with IPF.

More Fibrosis research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Kansas Medical Center
NIH-funded
Lab location1 site (Kansas City, United States)
Project startSeptember 15, 2025
Project endJune 30, 2030
Funding year2026
Award (this year)$687,576
NIH project number5R01HL176772-02
Project IDNIH-11411171 on NIH RePORTER

Who could benefit from this research

Could help

Adults with idiopathic pulmonary fibrosis who have available BALF and lung tissue samples and are or could be treated with current IPF therapies.

Less likely to help

Patients without IPF or those without available BALF/lung tissue samples for proteomic analysis may not benefit.

What this research studies

Researchers will analyze a large set of BALF and lung tissue samples from IPF patients around the world to find distinct protein patterns that track with survival and treatment response. They will look at autoinflammatory and immune signaling pathways to see if these endotypes predict who benefits from existing therapies. By validating these molecular clusters in a big patient cohort, the study seeks to move toward personalized management of IPF. The work builds on prior findings and uses advanced proteomics to connect biology with patient outcomes.

Why it matters

Potential benefit: If successful, patients with IPF could receive more personalized treatment plans based on their lung endotype, potentially improving survival and quality of life.

How similar studies have gone: Preliminary data in IPF endotypes suggest distinct prognostic protein patterns, with ongoing work aiming to validate these clusters in larger cohorts.

Where this research is happening

  • University of Kansas Medical Center
    Kansas City, United States
    Active

Researchers

  • Principal investigator: Matson, Scott Michael — University of Kansas Medical Center
  • Study coordinator: Matson, Scott Michael

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

  • 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

  • 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.