Chitin Analog AVR-25 Prevents Experimental Bronchopulmonary Dysplasia

Author:

Das Pragnya1,Acharya Suchismita23,Shah Dilip1,Agarwal Beamon4,Prahaladan Varsha1,Bhandari Vineet1

Affiliation:

1. Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, Pennsylvania, United States

2. Acceleration Laboratory, University of North Texas Health Science Center, Fort Worth, Texas, United States

3. AyuVis Research Inc, Fort Worth, Texas, United States

4. GenomeRxUS, Secane, Pennsylvania, United States

Abstract

AbstractInfants born extremely preterm are at a high risk of developing bronchopulmonary dysplasia (BPD) which is characterized by large, simplified alveoli, increased inflammation, disrupted and dysregulated vasculogenesis, decreased cell proliferation, and increased cell death in the lungs. Due to lack of specific drug treatments to combat this condition, BPD and its long-term complications have taken a significant toll of healthcare resources. AVR-25, a novel immune modulator experimental compound, was able to partially recover the pulmonary phenotype in the hyperoxia-induced experimental mouse model of BPD. We anticipate that AVR-25 will have therapeutic potential for managing human BPD.

Funder

AyuVis Research Inc.

Publisher

Georg Thieme Verlag KG

Subject

Critical Care and Intensive Care Medicine,Pediatrics, Perinatology and Child Health

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