BioAge Labs Reports Second Quarter 2026 Financial Results and Provides Business Updates
Rhea-AI Summary
BioAge Labs (NASDAQ:BIOA) reported second quarter 2026 collaboration revenue of $2.5 million, roughly flat year over year, and a net loss of $26.1 million (basic and diluted loss per share $0.58) versus a $21.6 million loss a year earlier. Research and development expenses rose to $24.4 million, mainly from higher BGE-102 program costs, while general and administrative expenses were $7.4 million.
As of June 30, 2026, BioAge held $381.3 million in cash, cash equivalents, and marketable securities and estimates funding through 2029. The first participant was dosed in QUELL-CV, a Phase 2 proof-of-concept trial of NLRP3 inhibitor BGE-102 in obesity with inflammation, with topline data expected in 2H 2026. A Phase 1b/2a trial in diabetic macular edema, QUELL-DME, is planned to start mid-2026, with data anticipated mid-2027. BioAge also advanced its APJ agonist programs and continued discovery collaborations with Novartis and Lilly ExploR&D.
Positive
- Cash and securities $381.3M at June 30, 2026; runway through 2029
- First patient dosed in QUELL-CV Phase 2 trial of BGE-102 in June 2026
- Phase 1 BGE-102 showed up to 98% IL-1β suppression and 86% median hsCRP reduction
- Collaboration revenue $2.45M in Q2 2026, roughly stable year over year
- Strategic collaborations with Novartis and Lilly ExploR&D continued with multiple targets under evaluation
Negative
- Net loss $26.1M in Q2 2026, up from $21.6M year over year
- R&D spend $24.4M in Q2 2026 vs. $19.8M, driven by BGE-102 costs
- Total operating expenses $31.8M vs. $27.2M in Q2 2025
- Weighted-average shares 44.8M vs. 35.9M a year earlier, indicating dilution
News Explained
As of
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| May 08 | Q1 earnings | Positive | +0.9% | Positive Phase 1 data, planned trials, follow-on financing, and funding runway |
| Mar 24 | FY earnings | Positive | -13.5% | BGE-102 progress, planned Phase 2a trial, financing, and funding through 2029 |
| Nov 06 | Q3 earnings | Neutral | -2.8% | BGE-102 Phase 1 dosing, APJ development, collaborations, and quarterly financial results |
| Aug 06 | Q2 earnings | Positive | -0.2% | Clinical pipeline progress, APJ partnership, patents, and reported financial position |
| Jul 31 | Partner sales update | Positive | -0.5% | Partner product sales and royalty revenue increased year over year |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
BioAge's tag-specific earnings history showed mostly negative or limited reactions despite generally positive clinical and pipeline updates, with an average move of -3.21%.
Key Terms
nlrp3 inhibitor medical
pharmacodynamic medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
First participant dosed in QUELL-CV, a Phase 2 dose-ranging proof-of-concept trial of BGE-102 measuring inflammatory and cardiometabolic biomarkers; topline data anticipated in the second half of 2026
QUELL-DME, Phase 1b/2a proof-of-concept trial of BGE-102 in diabetic macular edema, planned to initiate in mid-2026, with data anticipated in mid-2027; results expected to support development across inflammation-driven retinal diseases
Hosted R&D Day focused on NLRP3 inhibition, featuring Phase 1 data for BGE-102
EMERYVILLE, Calif., Aug. 05, 2026 (GLOBE NEWSWIRE) -- BioAge Labs, Inc. (NASDAQ: BIOA) ("BioAge" or "the Company"), a clinical-stage biopharmaceutical company developing therapeutic product candidates for cardiometabolic diseases by targeting the biology of human aging, today provided business updates and reported its second quarter 2026 financial results.
"NLRP3 sits at the apex of the inflammatory cascade that drives a range of diseases," said Kristen Fortney, Ph.D., CEO and co-founder of BioAge. "Our Phase 1 data show that BGE-102 is a potential best-in-class NLRP3 inhibitor: a well-tolerated once-daily pill that delivered up to
Second Quarter 2026 Business Highlights
BGE-102 clinical development: QUELL-CV Phase 2 trial
- In June 2026, BioAge announced that the first participant was dosed in QUELL-CV, a Phase 2 dose-ranging proof-of-concept trial of BGE-102, its oral, brain-penetrant NLRP3 inhibitor, measuring inflammatory and cardiometabolic biomarkers.
- QUELL-CV is a randomized, double-blind, placebo-controlled trial evaluating three once-daily oral doses of BGE-102 (30 mg, 60 mg, and 90 mg) against placebo in approximately 160 adults with obesity and elevated baseline inflammation.
- The primary endpoint is percent change from baseline in hsCRP, a pharmacodynamic measure of NLRP3 pathway inhibition, over 12 weeks of dosing.
- The trial is designed to characterize the dose-response relationship for BGE-102 and to support dose selection for further development, with topline data anticipated in the second half of 2026.
- QUELL-CV builds on the full Phase 1 dataset for BGE-102, in which the compound achieved up to
98% suppression of IL-1β at trough in an ex vivo whole-blood assay, along with median hsCRP reductions of86% from baseline at both 60 mg and 120 mg once daily. - BGE-102 was well tolerated across all dose levels evaluated, with no serious adverse events, no treatment-emergent adverse events leading to discontinuation, and no clinically meaningful changes in vital signs, ECGs, or laboratory values.
BGE-102 clinical development: QUELL-DME Phase 1b/2a trial
- Following an indication expansion into ocular diseases, the Company plans to initiate QUELL-DME, a Phase 1b/2a proof-of-concept trial of BGE-102 in patients with diabetic macular edema, in mid-2026; results are anticipated in mid-2027.
- QUELL-DME is designed to demonstrate pharmacodynamic target engagement for BGE-102 in the eye, potentially supporting future development in inflammation-driven retinal diseases.
R&D Day on NLRP3 inhibition
- In May 2026, BioAge hosted an R&D Day featuring Phase 1 clinical data for BGE-102 and the therapeutic rationale for targeting NLRP3 in multiple disease areas driven by inflammasome activation. A recording of the webcast is available at https://ir.bioagelabs.com/news-events/events.
APJ agonist program advancement
- BioAge continues to advance its oral and injectable APJ agonist development strategy, including a novel APJ agonist antibody that is the subject of an option agreement with JiKang Therapeutics. The Company intends to file its first IND for an APJ program by year-end 2026.
Strategic partnerships and discovery platform
- BioAge's multi-year research collaboration with Novartis, focused on discovering novel therapeutic targets at the intersection of aging biology and exercise physiology, continued to advance, with multiple targets under evaluation.
- The Company also continued to progress its strategic collaboration with Lilly ExploR&D for the development of therapeutic antibodies targeting novel metabolic aging targets.
Second Quarter 2026 Financial Results
Collaboration revenue was
Research and development expenses were
General and administrative expenses were
Net loss was
As of June 30, 2026, BioAge had approximately
About BioAge Labs, Inc.
BioAge is a clinical-stage biopharmaceutical company developing therapeutic product candidates for cardiometabolic diseases by targeting the biology of human aging. The Company's lead product candidate, BGE-102, is a potent, orally bioavailable, brain-penetrant small-molecule NLRP3 inhibitor being developed for diseases driven by inflammation, including retinal diseases such as diabetic macular edema. BGE-102 has completed a Phase 1 SAD/MAD trial demonstrating a well-tolerated profile and potential best-in-class reductions in hsCRP and other inflammatory biomarkers in participants with obesity and elevated inflammatory markers such as hsCRP. Phase 2 proof-of-concept data are anticipated in the second half of 2026, and Phase 1b/2a diabetic macular edema proof-of-concept data are anticipated in mid-2027. The Company is also developing long-acting injectable and oral small molecule APJ agonists for obesity. BioAge’s additional preclinical programs, which leverage insights from the Company’s proprietary discovery platform built on human longevity data, address key pathways involved in metabolic aging.
Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of, and made pursuant to the safe harbor provisions of, the Private Securities Litigation Reform Act of 1995. In some cases, you can identify forward-looking statements by terms such as “aim,” “may,” “will,” “should,” “expect,” “forecast,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words. All statements other than statements of historical fact contained in this press release, including without limitation statements regarding our plans to develop and commercialize our product candidates, including BGE-102 and our APJ programs, the potential for BGE-102 as a treatment for diabetic macular edema, the expected timeline for data readouts from our ongoing Phase 2 clinical trial, the expected timing and results of our ongoing or planned preclinical studies and clinical trials, risks associated with clinical trials, including our ability to adequately manage clinical activities for BGE-102 and our APJ programs, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, the timing of and our ability to obtain and maintain regulatory approvals, the clinical utility of our future product candidates, our commercialization, marketing and manufacturing capabilities and strategy, our expectations about the willingness of healthcare professionals to use our product candidates, the sufficiency of our cash, cash equivalents and marketable securities, general economic conditions, the impact of industry and market conditions on our operations, including fluctuating interest rates and inflation, increased volatility in the debt and equity markets, legislative or regulatory healthcare reforms in the United States, significant political, trade or regulatory developments, including tariffs, federal government shutdowns, or shifting priorities within the U.S. Food and Drug Administration, cybersecurity incidents, and global regional conflicts, and the plans and objectives of management for future operations and capital expenditures are forward-looking statements.
The forward-looking statements in this press release are only predictions and are based largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of known and unknown risks, uncertainties and assumptions, including those described under the headings “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” included in BioAge’s Quarterly Report on Form 10-Q filed with the U.S. Securities and Exchange Commission (SEC) on August 5, 2026, and BioAge’s other filings with the SEC filed from time to time.
Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond our control, you should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in our forward-looking statements may not be achieved or occur and actual results could differ materially from those projected in the forward-looking statements. Moreover, we operate in an evolving environment. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties. BioAge undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.
Contacts
PR: Chris Patil, media@bioagelabs.com
IR: Dov Goldstein, ir@bioagelabs.com
Partnering: partnering@bioagelabs.com
Web: https://bioagelabs.com
| BIOAGE LABS, INC. Unaudited Condensed Consolidated Statements of Operations (in thousands, except share and per share information) | ||||||||
| Three Months Ended | ||||||||
| June 30, | ||||||||
| 2026 | 2025 | |||||||
| Collaboration revenue | $ | 2,451 | $ | 2,412 | ||||
| Operating expenses: | ||||||||
| Research and development | $ | 24,365 | $ | 19,844 | ||||
| General and administrative | 7,419 | 7,339 | ||||||
| Total operating expenses | 31,784 | 27,183 | ||||||
| Loss from operations | (29,333 | ) | (24,771 | ) | ||||
| Other income (expense) | ||||||||
| Interest expense | (1 | ) | (201 | ) | ||||
| Interest and other income (expense), net | 3,438 | 3,420 | ||||||
| Gain (loss) from changes in fair value of warrants | (201 | ) | (11 | ) | ||||
| Total other income (expense), net | 3,236 | 3,208 | ||||||
| Net loss | $ | (26,097 | ) | $ | (21,563 | ) | ||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.58 | ) | $ | (0.60 | ) | ||
| Weighted-average common shares outstanding, basic and diluted | 44,838,893 | 35,850,037 | ||||||
| BIOAGE LABS, INC. Unaudited Condensed Consolidated Balance Sheets (in thousands, except share and per share information) | ||||||||
| June 30, | December 31, | |||||||
| 2026 | 2025 | |||||||
| Assets | ||||||||
| Current Assets: | ||||||||
| Cash and cash equivalents | $ | 73,964 | $ | 188,888 | ||||
| Marketable securities, current | 244,781 | 92,210 | ||||||
| Accounts receivable | 625 | 769 | ||||||
| Prepaid expenses and other current assets | 10,942 | 4,926 | ||||||
| Total current assets | 330,312 | 286,793 | ||||||
| Investments | 100 | 100 | ||||||
| Marketable securities | 62,518 | 4,032 | ||||||
| Property and equipment, net | 1,209 | 963 | ||||||
| Operating lease right-of-use assets | 2,582 | 2,785 | ||||||
| Other assets | 208 | 216 | ||||||
| Total assets | $ | 396,929 | $ | 294,889 | ||||
| Liabilities | ||||||||
| Current Liabilities: | ||||||||
| Accounts payable | $ | 5,653 | $ | 2,674 | ||||
| Accrued expenses and other current liabilities | 8,487 | 8,480 | ||||||
| Current portion of term loan | — | 2,648 | ||||||
| Operating lease liabilities, current | 714 | 582 | ||||||
| Deferred revenue | 4,363 | 5,754 | ||||||
| Total current liabilities | 19,217 | 20,138 | ||||||
| Warrant liability | 678 | 370 | ||||||
| Operating lease liabilities | 2,121 | 2,330 | ||||||
| Total liabilities | 22,016 | 22,838 | ||||||
| Commitments and Contingencies (Note 7) | ||||||||
| Stockholders’ Equity | ||||||||
| Preferred stock, | — | — | ||||||
| Common stock, | — | — | ||||||
| Additional paid-in-capital | 757,157 | 605,189 | ||||||
| Accumulated other comprehensive income (loss) | (478 | ) | 278 | |||||
| Accumulated deficit | (381,766 | ) | (333,416 | ) | ||||
| Total stockholders’ equity | 374,913 | 272,051 | ||||||
| Total liabilities and stockholders’ equity | $ | 396,929 | $ | 294,889 | ||||
