BIOABioAge Labs, Inc.

$6.35+30% 1Y

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

  1. 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
  2. May 8, 2026BioAge Labs Reports First Quarter 2026 Financial Results and Provides Business Updates.Earnings release · press release
  3. Mar 24, 2026BioAge Labs Reports Full Year 2025 Financial Results and Provides Business Updates from the Fourth Quarter of 2025.Earnings release · press release
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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.

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