BIOABioAge Labs, Inc.
$6.35+30% 1Y
$6.35
$4.9452 weeks$24.29
BIOA in its own filings
Nothing in BIOA's filing record raises a hard flag: no restatement, late filing, bankruptcy or delisting notice, and no auditor change next to one. That is the common case, not a distinction.
40
Events found in the filings · across 155 filings · the record starts in 2024
- Hard flags
- none
Hard flags
- Most recent filing
- Oct 2, 2026
Most recent filing · Form 8-K
- Record starts
- Jun 28, 2024
Record starts · the earliest filing Ryufin holds for this name
Details›
- Next results filingsame week as a year ago
- expected around Nov 5, 2026
- SEC comment-letter activity11 occurrences
- 2024-09-25
SEC EDGAR submissions index and 8-K item codes; 4.02 and 1.03 items are confirmed against the filing text.
What the company said
The company's own words from its current reports to the SEC, newest first
- Oct 2, 2026BioAge Labs, Inc. (the “Company”) recently announced that the first participant has been dosed in QUELL-DME, a randomized, controlled Phase 2 trial evaluating once-daily oral BGE-102, an NLRP3 inhibitor, in adults with diabetic macular edema (“DME”), and provided updates on the QUELL-DME Phase 2 trial design.Other event · Form 8-K
- May 8, 2026BioAge Labs Reports First Quarter 2026 Financial Results and Provides Business Updates.Earnings release · press release
- Mar 24, 2026BioAge Labs Reports Full Year 2025 Financial Results and Provides Business Updates from the Fourth Quarter of 2025.Earnings release · press release
- Jan 22, 2026On January 21, 2026, BioAge Labs, Inc., a Delaware corporation (the “Company”) entered into an underwriting agreement (the “Underwriting Agreement”) with Goldman Sachs & Co. LLC, Piper Sandler & Co. and Citigroup Global Markets Inc. as representatives of the underwriters named therein (the “Underwriters”), pursuant to …Material agreement entered · Form 8-K
- Jan 20, 2026Planned proof-of-concept clinical trial in DME On January 20, 2026, the Company announced indication expansion for oral NLRP3 inhibitor BGE-102. • Growing preclinical and clinical evidence points to central role of the inflammasome in multiple retinal diseases where inflammation is a key feature, including diabetic …Regulation FD disclosure · Form 8-K
- Jan 12, 2026Phase 1 Data for BGE-102 On January 12, 2026, the Company announced additional positive interim Phase 1 data for BGE-102, a novel brain-penetrant NLRP3 inhibitor, demonstrating potential for best-in-class hsCRP reduction in participants with elevated cardiovascular risk. • First BGE-102 multiple ascending dose (“MAD”) …Regulation FD disclosure · Form 8-K
- Dec 4, 2025Phase 1 Data for BGE-102 On December 4, 2025, the Company announced positive interim data from its ongoing Phase 1 single ascending dose (SAD) / multiple ascending dose (MAD) clinical trial evaluating BGE-102 a potent, structurally novel, orally available, brain-penetrant small molecule NLRP3 inhibitor being developed …Regulation FD disclosure · Form 8-K
- Nov 6, 2025BioAge Labs Reports Third Quarter 2025 Financial Results and Provides Business.Earnings release · press release
Quoted from SEC EDGAR filings. A current report is filed within four business days of the event it describes.
opening the record…
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