BioAge Reports Q1 Revenue of $2.77M, Exceeding Expectations
Written by Emily J. Thompson, Senior Investment Analyst
Updated: May 08 2026
0mins
Reports Q1 revenue $2.77M, consensus $1.08M. "The positive topline Phase 1 data we reported for BGE-102 in April reinforce our conviction that we have a potential best-in-class NLRP3 inhibitor: a well-tolerated, once-daily oral therapy that could deliver the anti-inflammatory efficacy of injectables," said Kristen Fortney, CEO and co-founder of BioAge. "Our focus now is execution. We plan to initiate two BGE-102 proof-of-concept trials by mid-2026 - a Phase 2 dose-ranging trial in cardiovascular risk, and a Phase 1b/2a trial in diabetic macular edema - advancing BGE-102 as a potential 'pipeline in a pill' across cardiometabolic and ocular diseases. With the $132.3 million we raised in our upsized follow-on offering earlier this year, we have the capital to drive both programs through key milestones."
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Analyst Views on BIOA
Wall Street analysts forecast BIOA stock price to rise
4 Analyst Rating
2 Buy
2 Hold
0 Sell
Moderate Buy
Current: 16.950
Low
15.00
Averages
37.00
High
73.00
Current: 16.950
Low
15.00
Averages
37.00
High
73.00
About BIOA
BioAge Labs, Inc. is a clinical-stage biopharmaceutical company developing therapeutic product candidates for metabolic diseases, such as obesity, by targeting the biology of human aging. Its lead product is BGE-102, a structurally novel, orally available small molecule NLRP3 inhibitor with high potency and brain penetration. In preclinical obesity models, BGE-102 resulted in weight loss as both a monotherapy and in combination with a GLP-1R agonist. Its pipeline includes novel, orally available, brain-penetrant small-molecule NLRP3 inhibitors to treat metabolic diseases and conditions driven by neuroinflammation, as well as novel APJ agonists for metabolic disorders. In preclinical obesity models, APJ agonism has demonstrated the ability to more than double the weight loss induced by a GLP-1R agonist while also restoring healthy body composition and improving muscle function.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Incentive Program Launch: The company introduced a three-year incentive program allowing for up to 235,000 performance-based share units to be awarded, aimed at motivating employees to enhance performance and drive long-term growth and competitiveness in the market.
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- Incentive Program Launch: The company introduced a three-year incentive program allowing for up to 235,000 performance-based share units, designed to motivate employees to achieve a 30% total shareholder return, thereby driving long-term growth for the company.
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- Global Market Approvals: Leqembi has been approved in 53 countries and is under regulatory review in 6 countries, demonstrating its broad acceptance in the global market and further solidifying BioArctic's leadership position in Alzheimer's disease treatment.
- Clinical Research Progress: Eisai's ongoing AHEAD 3-45 clinical study aims to evaluate the efficacy of lecanemab in early Alzheimer's disease patients, which is expected to provide crucial data for future market promotion and enhance BioArctic's competitive edge.
- Strategic Partnership: The long-term collaboration between BioArctic and Eisai since 2005 has positioned BioArctic advantageously in the development of Alzheimer's drugs, as it incurs no development costs and can earn milestone payments and royalties from global sales, ensuring financial stability.
See More
BioArctic and Eisai Present Leqembi Sales Forecast
- Future Sales Projection: Eisai's simulation indicates that Leqembi is expected to generate around JPY 300 billion (approximately SEK 17.6 billion) in sales for FY 2028, highlighting the drug's significant potential in the Alzheimer's market and likely boosting BioArctic's revenue.
- Global Approval Status: Leqembi has been approved in 53 countries and is under regulatory review in 6 others, demonstrating broad global recognition, while BioArctic's preparations for commercialization in the Nordics will further enhance its market position.
- Clinical Research Progress: Eisai's AHEAD 3-45 clinical study was fully recruited in October 2024, aiming to assess the efficacy of lecanemab in early Alzheimer's patients, with successful results providing strong support for future market promotion.
- Strategic Partnership: Since 2005, BioArctic's long-term collaboration with Eisai has positioned it prominently in the Alzheimer's treatment field, allowing BioArctic to avoid development costs while securing milestone payments and royalties from global sales, ensuring financial stability.
See More
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- Anti-Aging Therapy Progress: Avaí Bio, in collaboration with Austrianova, has completed the Master Cell Bank (MCB) of α-Klotho protein-overexpressing cells, marking a significant milestone that will advance clinical trial processes aimed at developing cell therapies for age-related diseases.
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See More
