NIH-funded research NIH-funded research

Developing a new treatment for idiopathic pulmonary fibrosis

Official title: Preclinical Development of a Novel Therapeutic Agent for Idiopathic Pulmonary Fibrosis

Funded at Fibrobiologics, LLC · NIH-10696538 · Data updated 2026-11-12

This study is looking at a new treatment called M10 that might help people with idiopathic pulmonary fibrosis (IPF) by reducing the harmful changes in their lung cells, with the hope of being more effective and having fewer side effects than current options.

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionFibrobiologics, LLC
NIH-funded
Lab location1 site (Charleston, United States)
Project startAugust 15, 2023
Project endJuly 31, 2025
Funding year2023
Award (this year)$299,295
NIH project number1R41HL167504-01A1
Project IDNIH-10696538 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are individuals diagnosed with idiopathic pulmonary fibrosis who are seeking new treatment options.

Less likely to help

Patients with other forms of lung disease or those who do not have idiopathic pulmonary fibrosis may not benefit from this research.

What this research studies

This research focuses on creating a novel peptide therapeutic agent aimed at treating idiopathic pulmonary fibrosis (IPF), a serious lung disease. The approach involves testing the effectiveness of a peptide called M10 in inhibiting the fibrotic processes in lung cells taken from IPF patients. By leveraging advancements in peptide formulation, the study aims to develop a treatment that is both effective and has fewer side effects compared to existing medications. The research will assess how well M10 can reduce the harmful characteristics of lung fibroblasts associated with IPF.

Why it matters

Potential benefit: If successful, this research could lead to a more effective and less toxic treatment option for patients suffering from idiopathic pulmonary fibrosis.

How similar studies have gone: While there have been advancements in peptide therapies, this specific approach targeting idiopathic pulmonary fibrosis is relatively novel and has not been extensively tested.

Where this research is happening

  • Fibrobiologics, LLC
    Charleston, United States
    Active

Researchers

  • Principal investigator: Bogatkevich, Galina S — Fibrobiologics, LLC
  • Study coordinator: Bogatkevich, Galina S

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.