NIH-funded research Sbir 2 grant

Developing a new treatment for Idiopathic Pulmonary Fibrosis

Official title: Translating a Novel Therapeutic Approach to the Treatment for Idiopathic Pulmonary Fibrosis

Funded at Vasarya Therapeutics, INC. · NIH-10915918 · Data updated 2026-11-12

This study is testing a new drug called VSR-H5 that aims to help people with Idiopathic Pulmonary Fibrosis (IPF) by targeting only the damaged areas of their lungs, with the hope of improving their health without causing the side effects that come with current treatments.

Quick facts

Grant typeSbir 2 grant
Study typeNIH-funded research
Funding institutionVasarya Therapeutics, INC.
NIH-funded
Lab location1 site (Camden, United States)
Project startSeptember 15, 2024
Project endAugust 31, 2025
Funding year2024
Award (this year)$356,250
NIH project number1R44HL170936-01A1
Project IDNIH-10915918 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 alternative treatment options.

Less likely to help

Patients with other forms of lung disease or those who do not have a diagnosis of Idiopathic Pulmonary Fibrosis may not benefit from this research.

What this research studies

This research aims to create a novel drug candidate specifically designed to treat Idiopathic Pulmonary Fibrosis (IPF), a serious and currently incurable lung disease. The approach focuses on a compound called VSR-H5, which targets only the fibrotic areas of the lungs in patients, avoiding damage to healthy tissues. The research will involve testing this compound in laboratory settings and animal models to assess its effectiveness and safety. By selectively inhibiting the activation of harmful cells involved in fibrosis, this treatment hopes to improve patient outcomes without the severe side effects associated with existing therapies.

Why it matters

Potential benefit: If successful, this research could provide a more effective and safer treatment option for patients suffering from Idiopathic Pulmonary Fibrosis.

How similar studies have gone: While there have been advancements in IPF treatments, this specific approach using the VSR-H5 compound is novel and has not been extensively tested in clinical settings.

Where this research is happening

  • Vasarya Therapeutics, INC.
    Camden, United States
    Active

Researchers

  • Principal investigator: Hu, Ping — Vasarya Therapeutics, INC.
  • Study coordinator: Hu, Ping

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.