NIH-funded research Career grant

Adrenergic Nerves and Noradrenaline in Lung Fibrosis

Official title: Adrenergic Nerves, Noradrenaline, and Myofibroblasts in Idiopathic Pulmonary Fibrosis

Funded at Yale University · NIH-11351083 · Data updated 2026-11-12

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.

More Fibrosis research and trials

Quick facts

Grant typeCareer grant
Study typeNIH-funded research
Funding institutionYale University
NIH-funded
Lab location1 site (New Haven, United States)
Project startJuly 5, 2026
Project endJune 30, 2031
Funding year2026
Award (this year)$165,564
NIH project number1K08HL185896-01
Project IDNIH-11351083 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are adults with IPF or related fibrotic lung conditions who may participate in future translational studies or donate samples for related research.

Less likely to help

This career development grant does not directly enroll patients in a specific trial today.

What this research studies

This grant supports a clinician-scientist’s career development to study the neurobiology of idiopathic pulmonary fibrosis using experimental models and mentors with expertise in adrenergic signaling, tissue remodeling, and genomics. The program emphasizes training, coursework, and a research plan that will establish independent work distinct from the mentor’s projects, with significant institutional support. The work aims to translate insights about adrenergic nerves and noradrenaline’s role in IPF toward future therapies for patients. The applicant will dedicate 75% effort to career development and research to become an independent, funded physician-scientist.

Why it matters

Potential benefit: If successful, patients with IPF could benefit from a better understanding of nerve-based drivers of fibrosis, potentially informing new treatment strategies.

How similar studies have gone: Prior work has shown adrenergic signaling can drive fibrosis in experimental lung models, supporting potential translational relevance.

Where this research is happening

  • Yale University
    New Haven, United States
    Active

Researchers

  • Principal investigator: Ishikawa, Genta — Yale University
  • Study coordinator: Ishikawa, Genta

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.