Our program is a clinical stage, oral small molecule drug candidate targeting upstream of TNFa, IL-23, a4b7, S1P, TL1A & JAKi biology, converging on validated pathways that enables combination with approved blockbuster drugs allowing broader anti-inflammatory effects.
Lacking Efficacy of Current Therapies is Apparent in Patient Response
Sources: Solitano V, Jairath V, Magro F, Armuzzi A, Peyrin-Biroulet L, Danese S. Breaking the therapeutic ceiling in inflammatory bowel disease: myth or reality? Lancet Gastroenterol Hepatol. 2026. · Fairbrass KM, Costantino SJ, Gracie DJ, Ford AC. Prevalence of irritable bowel syndrome-type symptoms in patients with inflammatory bowel disease in remission: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2020;5:1053–1062.
A growing global market where existing therapies leave meaningful room for a differentiated, combinable oral therapy.
Sources: US Market Sales — FY2025 net sales, bottom up from company FY2025 results (AbbVie, J&J, Takeda) and SEC filings; estimated UC/CD split modeled by FDA approval timing per indication. Epidemiology: CDC; Lewis et al., Gastroenterology 2023;165(5):1197–1205.
Azuriya inhibits Ref-1, a novel transcription-factor regulator that sits upstream of validated downstream targets. One oral small molecule converging on multiple validated pathways at once.
Explore the Science
APX3330 has been studied across 3 indications in 14 Phase 1 and Phase 2 clinical trials, with approximately 400 patients dosed and no serious drug-related adverse events.
Contact our team for investor, partnership, and clinical inquiries, or explore our published science.