Developing selective
NLRP3 inflammasome inhibitors
for severe inflammatory diseases
Science/Technology
Our drug discovery platform is focused on developing selective antagonists of the NLRP3 inflammasome, an inflammatory pathway critical to the development of a wide variety of diseases including acute lung injury, ARDS, Bronchopulmonary Dysplasia, systemic sepsis, acute liver and kidney injury, and pneumonia.
Our lead candidate, AZM-152, is a small molecule, RHAMM-derived antagonist that blocks a key upstream priming signal involved in the aberrant activation of the NLRP3 inflammatory cascade.
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Initial indications target severe inflammatory pulmonary diseases with significant unmet needs:
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Acute Respiratory Distress Syndrome (ARDS)
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Bronchopulmonary Dysplasia (BPD), a consequence of acute lung injury in preterm infants
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Acute Exacerbations of Idiopathic Pulmonary Fibrosis (IPF)
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Severe viral pneumonia such as Influenza A and COVID-19 infection
For many inflammatory and fibrotic lung diseases, no effective preventative or therapeutic treatments exist. With limited options for disease management, these severe and acute lung conditions exert a considerable burden on patients, families, and healthcare providers, including higher rates of mortality, longer lengths of stay in intensive care units, and life-long morbidities.
Additional indications for clinical development include other NLRP3 inflammasome-mediated severe inflammatory diseases of the lungs, liver and kidneys.
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