# Phase 1 Safety, Pharmacokinetic study followed by Phase 2a Proof-of-Concept study of AVR-48, a small molecule macrophage modulator to prevent bronchopulmonary dysplasia in neonates

> **NIH NIH R44** · AYUVIS RESEARCH, INC. · 2024 · $895,365

## Abstract

ABSTRACT
Bronchopulmonary Dysplasia (BPD) is the most common chronic respiratory disease in infants and is a
devastating condition that disrupts the developmental program of the lung secondary to preterm birth. Preterm
neonates exposed to mechanical ventilation develop moderate to severe BPD that affects their survival (10%
mortality) and respiratory function, and to date, there are no specific drugs available to prevent or treat this life-
threatening condition. The pathologic hallmarks of BPD are hyperoxia-induced pulmonary inflammation,
increased cell death, dysregulated angiogenic factors culminating in impaired alveolarization, dysregulated
vascularization of the lung and pulmonary hypertension. AyuVis Research, Inc, is developing a novel class of
low molecular weight natural oligosaccharide-derived small molecules and the lead compound AVR-48 which
activate macrophage to an intermediary phenotype via TLR4/CD163 signaling in human blood and mouse spleen
mononuclear cells. In both mouse and preterm lamb BPD models, the lead candidate AVR-48 block inflammatory
mediators in lung and upregulation of endogenous vascularization pathways. The lead compound AVR-48
enhances production of certain host anti-inflammatory molecule such as IL-10 and growth factor VEGF with
vascularization effects remaining local to lungs, improving lung vascularization/alveolization leading to improved
lung function and survival. AVR-48 also prevents the development of BPD associated pulmonary hypertension.
Importantly, we have assessed the Maximum Tolerated Dose and determined the NOAEL dose of AVR-48 in
both juvenile and adult rats, in adult dogs and efficacy/safety doses in preterm lamb BPD model via IV dosing,
which we will use to determine the dose ranges of our proposed clinical studies. We have demonstrated all these
above-mentioned therapeutic effects in two BPD models: intraperitoneal injection of AVR-48 prevents hyperoxia-
induced BPD in a neonatal mice pup model at 10mg/kg dose and intravenous injection in invasive mechanical
ventilator induced BPD in pre-term lambs at 3.0 mg/kg dose. In order to advance the lead candidate AVR-48,
AyuVis is submitting IND application to the FDA and preparing for Phase-1 and Phase-2a clinical trials. Here we
propose two clinical trial: 1) Evaluate the Safety and PK parameters of AVR-48 in a Phase-I SAD and MAD
clinical trial in healthy adult volunteers and 2) Evaluate the Safety, PK and efficacy of AVR-48 in an exploratory
Phase-2a clinical trial in pre-term infants at risk of developing BPD.
The completion of both clinical trials will provide the essential safety and pharmacokinetic data required to
continue the product development of AVR-48. The data yielded through the completion of the aims of this project
will lead the way to the development of future clinical project, including a Phase 2b/3 clinical trial aimed to assess
the efficacy of AVR-48 in preterm infants at risk of developing BPD using larger sample size. Ultimatel...

## Key facts

- **NIH application ID:** 10820785
- **Project number:** 1R44HD112276-01A1
- **Recipient organization:** AYUVIS RESEARCH, INC.
- **Principal Investigator:** Suchismita Acharya
- **Activity code:** R44 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $895,365
- **Award type:** 1
- **Project period:** 2024-04-12 → 2027-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10820785

## Citation

> US National Institutes of Health, RePORTER application 10820785, Phase 1 Safety, Pharmacokinetic study followed by Phase 2a Proof-of-Concept study of AVR-48, a small molecule macrophage modulator to prevent bronchopulmonary dysplasia in neonates (1R44HD112276-01A1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10820785. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*