NIH-funded research Sbir 2 grant

Developing a new treatment for bronchopulmonary dysplasia in infants

Official title: Development of a systems pharmacology agent for treatment of bronchopulmonary dysplasia

Funded at Reneurogen, LLC · NIH-11311467 · Data updated 2026-11-12

This study is working on a new medicine to help treat bronchopulmonary dysplasia (BPD) in premature babies, and the researchers are making sure it’s safe to test in humans so that it can eventually be available to those who need it.

More Bronchopulmonary Dysplasia research and trials

Quick facts

Grant typeSbir 2 grant
Study typeNIH-funded research
Funding institutionReneurogen, LLC
NIH-funded
Lab location1 site (Elm Grove, United States)
Project startJune 15, 2023
Project endMay 31, 2026
Funding year2025
Award (this year)$50,000
NIH project number3R44HL166018-02S1
Project IDNIH-11311467 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are premature infants diagnosed with bronchopulmonary dysplasia.

Less likely to help

Patients who are not premature or do not have bronchopulmonary dysplasia may not benefit from this research.

What this research studies

This research focuses on creating a novel drug candidate aimed at treating bronchopulmonary dysplasia (BPD), a serious lung condition affecting premature infants. The drug, known as N-acetyl-lysyltyrosylcysteine amide (KYC), has shown promising results in animal models. The research team is working on regulatory planning and engaging with the FDA to ensure the drug can be safely tested in humans. By collaborating with experts in pediatric drug development, the team aims to navigate the complexities of bringing this treatment to market.

Why it matters

Potential benefit: If successful, this research could lead to a new effective treatment for infants suffering from bronchopulmonary dysplasia, improving their lung health and overall quality of life.

How similar studies have gone: Previous research has shown success with similar pharmacological approaches in treating chronic lung diseases in infants, indicating potential for this novel treatment.

Where this research is happening

  • Reneurogen, LLC
    Elm Grove, United States
    Active

Researchers

  • Principal investigator: Naylor, Stephen — Reneurogen, LLC
  • Study coordinator: Naylor, Stephen

Related research

Other NIH-funded projects on the same topics.

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.