# Mentorship of Early-Career Clinicians in Bronchopulmonary Dysplasia Drug Therapies

> **NIH NIH K24** · UNIV OF NORTH CAROLINA CHAPEL HILL · 2020 · $122,504

## Abstract

Premature infants with bronchopulmonary dysplasia (BPD) often die and survivors have life-long morbidities.
BPD is the most common morbidity of prematurity, affecting >18,000 infants per year. The NIH defines BPD as
the receipt of exogenous oxygen or positive airway pressure at 36 weeks adjusted age. The costs of BPD are
both social and economic and are measured in impaired childhood health and quality of life, family stress and
economic hardship, and increased healthcare costs. Because the consequences of BPD are catastrophic,
neonatologists frequently use drugs without proven efficacy in an attempt to prevent and treat BPD.
Unfortunately, there are no FDA approved drugs for the prevention or treatment of BPD. Developing safe and
effective drugs for BPD is an ideal opportunity to improve public health and provides a platform to develop
trainees’ expertise in trial design, regulatory requirements, and rigorous quantitative methods that will be
applied to their own independent research career.
The investigator, Dr. Matthew M. Laughon, MD, MPH is a practicing neonatologist with an MPH in
epidemiology and training in clinical pharmacology. Dr. Laughon has secured access for trainee development
to The University of North Carolina at Chapel Hill programs including the Division of Neonatal-Perinatal
Medicine, the Gillings School of Public Health, and the Eshelman School of Pharmacy. Dr. Laughon also has a
longstanding academic partnership with the world’s largest academic research organization, the Duke Clinical
Research Institute. Through these programs, Dr. Laughon will mentor trainees at UNC and Duke and provide a
pathway for trainees to secure advanced training in epidemiology, clinical pharmacology, or
pharmacoepidemiology. Beginning clinician investigators will follow a logical progression including designing
an original hypothesis driven research project, completing didactic studies, participation in one on one and
group mentoring, and regular evaluation and feedback. Trainees will focus on the preparation and conduct of
early-phase drug trials in neonatal lung disease, primarily BPD. Proof of the feasibility of these expectations is
provided by current and former trainees who have achieved success in quantitative, patient-oriented research.
Determining the PK and safety of drugs for BPD in premature infants is an urgent, unmet public health need.
Investigating drugs for BPD represents an ideal opportunity to approach the problem of the research gap of
drugs in premature infants because: 1) Premature infants with BPD have life-long morbidities; 2) There are no
drugs that have been proven to prevent or treat BPD; 3) Neonatologists are commonly using drugs in
premature infants without appropriate dosing and safety studies; and 4) Preventing mortality and morbidities
associated with premature birth has life-long benefits. The proposed trainee-led research project will use an
opportunistic study design of 10 commonly used drugs that will provide a p...

## Key facts

- **NIH application ID:** 9995561
- **Project number:** 5K24HL143283-02
- **Recipient organization:** UNIV OF NORTH CAROLINA CHAPEL HILL
- **Principal Investigator:** Matthew Laughon
- **Activity code:** K24 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $122,504
- **Award type:** 5
- **Project period:** 2019-08-15 → 2024-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9995561

## Citation

> US National Institutes of Health, RePORTER application 9995561, Mentorship of Early-Career Clinicians in Bronchopulmonary Dysplasia Drug Therapies (5K24HL143283-02). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/9995561. Licensed CC0.

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