
BioAge was founded in 2015 to develop therapies for metabolic disease by targeting biology associated with human aging. The company became publicly traded in 2024 (Nasdaq: BIOA). In 2024, BioAge discontinued development of its apelin receptor agonist azelaprag after observing liver enzyme elevations in clinical testing and subsequently prioritized its NLRP3 program.
BioAge focuses on metabolic disease and related cardiometabolic risk, with inflammation as a central biological theme. The company’s current lead development effort is positioned around chronic inflammation in obesity and cardiovascular risk-factor settings. In January 2026, BioAge also disclosed an expansion of the lead program into ophthalmology as an additional proof-of-concept direction.
BioAge uses human data-driven discovery approaches to identify targets linked to aging-associated disease biology and translate them into small-molecule therapies. Its lead modality is an orally available small-molecule inhibitor of NLRP3, designed to modulate inflammasome-driven inflammation. The company has also described earlier-stage work across additional targets, including programs related to metabolic signaling pathways.
Kristen Fortney is Chief Executive Officer.
BioAge’s recent public profile has been driven primarily by internal development and capital markets activity rather than a partner-led pipeline strategy. The company’s external footprint includes academic and clinical site networks supporting Phase I execution and biomarker-driven development.
BioAge develops small-molecule therapies for metabolic disease by targeting biology associated with human aging. The company’s current lead focus is inflammasome-driven inflammation, with programs designed to translate biomarker and human-data insights into medicines suitable for broad cardiometabolic populations.
BioAge is focused on metabolic disease and cardiometabolic risk, including inflammation-linked risk-factor profiles commonly seen in obesity. The company has also signaled interest in adjacent indications where systemic inflammation is a driver of disease biology.
BGE-102 is BioAge’s lead program. It is an oral, brain-penetrant small-molecule NLRP3 inhibitor in Phase I (SAD/MAD). BioAge has described initial development in obesity and cardiovascular risk-factor populations and has also disclosed an expansion of BGE-102 into diabetic macular edema as an additional clinical direction. Other programs are earlier stage and have been described at a higher level without the same degree of asset-by-asset public detail.
January 2026: BioAge reported additional positive interim Phase I data for BGE-102, including biomarker reductions consistent with anti-inflammatory activity in participants with elevated cardiovascular risk.
January 2026: BioAge also disclosed an expansion of BGE-102 development into diabetic macular edema as an ophthalmology proof-of-concept step.
December 2025: BioAge reported positive interim Phase I data for BGE-102 and continued Phase I execution.
BioAge’s recent updates have focused on interim Phase I biomarker readouts for BGE-102, including reductions in inflammation markers in participants with elevated baseline risk. The company has positioned these findings as supportive of advancement into patient studies designed to test clinical relevance in cardiometabolic populations.
Near-term milestones include completing Phase I data readouts for BGE-102 and initiating a Phase IIa study path in 2026, alongside clarifying the initial patient-study designs and endpoints for both cardiometabolic and ophthalmology proof-of-concept plans.
BioAge is led by a CEO with a data-driven drug discovery background and operates with an organization structured for biomarker-forward early clinical development, reflecting a strategy that prioritizes rapid translation from mechanistic readouts to patient proof-of-concept.
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