ME on NASDAQ

Chrome Holding Co.

Logo: 23andMe, Public domain, via Wikimedia Commons5

American personal genomics company

23andMe Research Institute is an American personal genomics and biotechnology nonprofit public benefit company based in Palo Alto, California. It provides a direct-to-consumer genetic testing service in which customers submit a saliva sample that is laboratory analysed using single nucleotide polymorphism (SNP) genotyping to generate reports on the customer's ancestry and genetic predispositions to health-related conditions. The company's name is derived from the 23 pairs of chromosomes in a diploid human cell.3 It was founded by Paul Cusenza, Anne Wojcicki and Linda Avey.1 Wikipedia text CC BY-SA 4.0

Price unavailable

Last updated Oct 21, 2026.

Overview

$189.9MRevenue, fiscal 20256
-$280.9MNet income, fiscal 20257
Apr 2006Founded1

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  • TickerME on NASDAQ1
  • Industrybiotechnology industry1
  • HeadquartersSouth San Francisco1
  • Legal formprivately held company, Delaware corporation1
  • Incorporated inDE8
  • Business address870 Market Street, Room 415, San Francisco, Ca 941028
  • Filer categoryAccelerated filer8
  • LEI529900FU5IIBCXYHHX254
  • StatusActive4
  • LEI statusIssued and current4
  • Registered addressc/o Corporation Service Company, 251 Little Falls Drive, 19808 Wilmington, United States4
  • Registered withDivision of Corporations, Department of State, 60061714

23andMe Research Institute is an American personal genomics and biotechnology nonprofit public benefit company based in Palo Alto, California. It provides a direct-to-consumer genetic testing service in which customers submit a saliva sample that is laboratory analysed using single nucleotide polymorphism (SNP) genotyping to generate reports on the customer's ancestry and genetic predispositions to health-related conditions. The company's name is derived from the 23 pairs of chromosomes in a diploid human cell.3

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2025

52.7%Gross margin6
-126.7%Operating margin6
-147.9%Net margin7
-13.5%Revenue growth, 20256
-$170.5MFree cash flow6

Where the money goes

Where each dollar of revenue went, fiscal 2025

  • Cost of revenue47¢$89.9M
  • Research and development53¢$101.6M
  • Income tax0¢$41.0K

Out of $189.9M in revenue.67 The company lost money this year.

Financial statements

Revenue1112136$189.9M in 2025−38% since 2020
0$100.0M$200.0M$300.0M$400.0M2020: $305.5M$305.5M20202021: $243.9M$243.9M2021−20%2022: $271.9M$271.9M2022+11%2023: $299.5M$299.5M2023+10%2024: $219.6M$219.6M2024−27%2025: $189.9M$189.9M2025−14%
Gross profit1112136$100.0M in 2025−27% since 2020
0$50.0M$100.0M$150.0M2020: $137.4M$137.4M20202021: $117.0M$117.0M2021−15%2022: $132.9M$132.9M2022+14%2023: $132.3M$132.3M2023−0%2024: $97.9M$97.9M2024−26%2025: $100.0M$100.0M2025+2%
Operating income1112136-$240.6M in 2025−7% since 2020
-$600.0M-$400.0M-$200.0M02020: -$258.4M-$258.4M20202021: -$185.2M-$185.2M2021−28%2022: -$254.2M-$254.2M2022+37%2023: -$223.1M-$223.1M2023−12%2024: -$581.7M-$581.7M2024+161%2025: -$240.6M-$240.6M2025−59%
Net income11127-$280.9M in 2025+12% since 2020
-$800.0M-$600.0M-$400.0M-$200.0M02020: -$250.9M-$250.9M20202021: -$183.6M-$183.6M2021−27%2022: -$217.5M-$217.5M2022+18%2023: -$311.7M-$311.7M2023+43%2024: -$666.7M-$666.7M2024+114%2025: -$280.9M-$280.9M2025−58%
Fiscal year2019202020212022202320242025
Revenue$305.5M11$243.9M12$271.9M13$299.5M6$219.6M6$189.9M6
Cost of revenue$168.0M11$126.9M12$138.9M13$167.2M6$121.7M6$89.9M6
Gross profit$137.4M11$117.0M12$132.9M13$132.3M6$97.9M6$100.0M6
Research and development$181.3M11$159.9M12$189.4M13$116.0M6$105.0M6$101.6M6
Operating expenses$387.1M13$355.4M6$679.6M6$340.6M6
Operating income-$258.4M11-$185.2M12-$254.2M13-$223.1M6-$581.7M6-$240.6M6
Income before tax-$221.0M13-$314.4M13-$666.6M13
Income tax$011$012-$3.5M13-$2.8M6$73.0K6-$41.0K6
Net income-$250.9M11-$183.6M12-$217.5M7-$311.7M7-$666.7M7-$280.9M7
Earnings per share-$13.806-$28.016-$10.886
Earnings per share (diluted)-$13.806-$28.016-$10.886
Shares (weighted, basic)361.5M shares1322.6M shares623.8M shares625.8M shares6
Shares (weighted, diluted)361.5M shares1322.6M shares623.8M shares625.8M shares6

Compare Chrome Holding Co. with another company

Corporate structure

Chrome Holding Co. sits at the top of its group. 12 entities, 1 country on record. Switch between the flow chart and the network, and select any entity to see its details.

Major holders of Chrome Holding Co.

  • Farallon Capital Partners, L.P. Filed SCHEDULE 13G on Chrome Holding Co., latest Jun 20, 2025
  • ABeeC 2.0, LLC Filed SCHEDULE 13D/A on Chrome Holding Co., latest Jun 16, 2025 (13 filings since Apr 17, 2024)
  • Zentree Investments Ltd Filed SCHEDULE 13D/A on Chrome Holding Co., latest Apr 1, 2025 (6 filings since Nov 13, 2024)
  • GSK Filed SC 13D/A on Chrome Holding Co., latest Nov 15, 2024 (4 filings since Nov 4, 2022)
  • VANGUARD GROUP INC Filed SC 13G/A on Chrome Holding Co., latest Nov 12, 2024 (4 filings since Feb 9, 2023)
  • SC US (TTGP), LTD. Filed SC 13G/A on Chrome Holding Co., latest Oct 21, 2024
  • BlackRock Filed SC 13G/A on Chrome Holding Co., latest Jul 8, 2024 (3 filings since Feb 13, 2023)
  • NewView Capital Fund I, L.P. Filed SC 13G on Chrome Holding Co., latest Feb 14, 2023
  • FMR LLC Filed SC 13G/A on Chrome Holding Co., latest Feb 9, 2023 (5 filings since Dec 10, 2021)
  • CITADEL ADVISORS LLC Filed SC 13G/A on Chrome Holding Co., latest Feb 14, 2022
  • MARSHALL WACE, LLP Filed SC 13G/A on Chrome Holding Co., latest Feb 14, 2022
  • Chrome Holding Co. Sunnyvale, California, United States
    • 23andMe Pharmacy Holdings, Inc. Subsidiary · Delaware, United States
    • 23andMe, Inc. Subsidiary · Delaware, United States
    • Lemonaid Community Pharmacy Subsidiary · Missouri, United States
    • Lemonaid Health Inc. Subsidiary · Delaware, United States
    • Lemonaid Pharmacy Holdings, Inc. Subsidiary · Delaware, United States
    • LPharm CS LLC Subsidiary · Delaware, United States
    • LPharm INS LLC Subsidiary · Delaware, United States
    • LPharm RX LLC Subsidiary · Delaware, United States
    • LPRXOne LLC Subsidiary · Missouri, United States
    • LPRXThree LLC Subsidiary · Missouri, United States
    • LPRXTwo LLC Subsidiary · Missouri, United States

Built from parent and subsidiary links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); subsidiaries listed in Exhibit 21 of annual reports filed with the SEC; major holders from Schedules 13D and 13G. Each entity in the chart links to its source.

What it owns

What Chrome Holding Co. reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.

Property and equipment

ItemLatestA year beforeChange
Computer equipment and software$41.6M6 Mar 31, 2025$35.9M6 Mar 31, 2024+15.9%
Property and equipment, before depreciation$39.2M6 Mar 31, 2025$81.4M6 Mar 31, 2024−51.8%
Accumulated depreciation$37.9M6 Mar 31, 2025$58.9M6 Mar 31, 2024−35.6%
Property and equipment, net$1.3M6 Mar 31, 2025$22.5M6 Mar 31, 2024−94.4%
Operating-lease assets (leased space)$533.0K6 Mar 31, 2025$38.1M6 Mar 31, 2024−98.6%

Real estate and locations

ItemLatestA year beforeChange
Area of real estate17,312 sq ft6 Sep 16, 2024

Investments

ItemLatestA year beforeChange
Cash and cash equivalents$38.2M6 Mar 31, 2025$216.5M6 Mar 31, 2024−82.3%

Intangibles and goodwill

ItemLatestA year beforeChange
Goodwill$06 Mar 31, 2024$351.7M13 Mar 31, 2023−100.0%
Finite-lived intangibles, gross$67.3M6 Mar 31, 2025$67.3M6 Mar 31, 20240%
Accumulated amortization$42.0M6 Mar 31, 2025$34.0M6 Mar 31, 2024+23.3%
Finite-lived intangibles, net$25.3M6 Mar 31, 2025$33.3M6 Mar 31, 2024−23.8%

Inventory

ItemLatestA year beforeChange
Inventory, total$15.6M6 Mar 31, 2025$12.5M6 Mar 31, 2024+24.8%

Properties, in its own words

Our corporate headquarters is located in San Francisco, California, and consists of 386 square feet of office space under a lease that expires on November 30, 2025. We also lease 65,340 square feet of space in South San Francisco, California, 154,987 square feet of office space in Sunnyvale, California and 23,731 square feet of office space in St. Louis, Missouri, under leases that expire on January 31, 2027, July 31, 2031 and June 30, 2026, respectively.

In December 2024, in connection with the November 2024 Reduction Plan, the Company abandoned the lab facility in South San Francisco, California (the “South San Francisco Facility”). Subsequently, in March 2025, in connection with the Chapter 11 Cases, the Company also abandoned the facility in Sunnyvale, California (the “Sunnyvale Facility”). See Note 4, “Discontinued Operations,” and Note 12, “Leases,” for additional details. The leases for the Sunnyvale Facility and the South San Francisco Facility were rejected or are subject to a pending motion to reject pursuant to the Chapter 11 Cases. The final allowed claim amounts related to these lease rejections had not been determined as of the date of this Form 10-K.

The rest of Item 2

We use the St. Louis, Missouri facility for healthcare and pharmacy operations.

Item 2 of the 10-K filed Jun 11, 2025.19

The story

Founded by Anne Wojcicki, Linda Avey and Paul Cusenza on Apr 2006.1

History

Founding and early growth (2006–2017)

Linda Avey, Paul Cusenza, and Anne Wojcicki founded 23andMe in 2006 to offer genetic testing and interpretation to individuals. Investment documents from 2007 suggest that 23andMe also intended to develop a database for research purposes. In 2007, Google invested $3.9 million in the company, along with Genentech, New Enterprise Associates, and Mohr Davidow Ventures. Wojcicki and Google co-founder Sergey Brin were married at the time.

Cusenza left the company in 2007 and Avey departed in 2009.

In 2012, 23andMe raised $50 million in a Series D venture round, nearly doubling its total capital of $52.6 million. In 2015, a $115 million Series E round brought total capital to $241 million. By late 2017, the company had raised approximately $250 million at a $1.75 billion valuation.

GlaxoSmithKline partnership (2018–2023)

On July 25, 2018, 23andMe announced a partnership with GlaxoSmithKline (GSK) in which GSK would use data from consenting customers to support drug development, investing $300 million in the company. In January 2022, the partnership was extended until July 2023 with an additional $50 million payment. In July 2020, the partnership produced its first clinical trial: a jointly developed cancer therapy.

Going public and Lemonaid acquisition (2020–2021)

The company was based in Mountain View, California, initially in North Bayshore and then downtown, until 2019, when it moved to larger headquarters in Sunnyvale. In January 2020, 23andMe laid off about 100 employees in its consumer testing division.

In December 2020, the company raised approximately $82.5 million in a Series F round, bringing total funding to over $850 million. In February 2021, 23andMe announced a merger with Sir Richard Branson's special-purpose acquisition company, VG Acquisition Corp, in a $3.5 billion transaction. The merger closed in June 2021; the combined entity, renamed 23andMe Holding Co., began trading on the Nasdaq under the ticker symbol "ME".

In October 2021, 23andMe acquired Lemonaid Health, a telehealth company, for $400 million, with the deal closing in November.

Decline and bankruptcy (2022–2025)

After reaching a market capitalization of approximately $6 billion following its public listing, 23andMe's valuation fell sharply; by early 2024 it stood at roughly 2% of its peak. Contributing factors included the company's persistent lack of profitability and the absence of recurring revenue from its one-time DNA test kits.

Read the full text

Wojcicki made several attempts to take the company private. An initial bid of $2.53 per share in February 2024 did not proceed. In July 2024, she offered 40 cents per share for all outstanding shares not already owned by her, but a special committee of the board rejected the proposal. In September 2024, all seven independent board members resigned. The company subsequently filed with the SEC indicating it was no longer open to third-party acquisition offers. Users attempting to delete their genetic data discovered that the company retained it for three years to comply with legal obligations. Further layoffs followed in November 2024.

In January 2025, 23andMe disclosed it needed additional liquidity and was exploring strategic alternatives including a potential sale. Wojcicki made a third offer of 41 cents per share in March 2025. On March 23, 2025, 23andMe filed for Chapter 11 bankruptcy protection as part of a plan to sell its assets, listing assets and liabilities each between $100 million and $500 million. Wojcicki stepped down as CEO and was replaced by CFO Joe Selsavage. Trading in the company's shares was suspended on March 31 and the stock was delisted from Nasdaq, subsequently trading over-the-counter.

California Attorney General Rob Bonta issued a consumer privacy alert reminding Californian users of their right to request deletion of their genetic data.

TTAM acquisition (2025)

The initial bankruptcy auction was won by Regeneron Pharmaceuticals for $256 million. As part of that agreement, Regeneron would have acquired all units of 23andMe except its telehealth service Lemonaid Health. However, the bankruptcy court reopened the auction after Wojcicki argued that her nonprofit, TTAM Research Institute, had been unfairly excluded from the bidding process. In the final round, TTAM submitted a winning bid of $305 million. 23andMe had separately announced it would cease being a public company and deregister from the SEC effective June 6, 2025.

TTAM completed the acquisition of substantially all of 23andMe's assets—including the Personal Genome Service, Research Services, and Lemonaid Health—on July 14, 2025. TTAM committed to honouring 23andMe's existing privacy policies, establishing a Consumer Privacy Advisory Board, and restricting future sale or transfer of genetic data unless any new owner adopted equivalent privacy protections.

Product history and pricing

Product tiers

In late 2009, 23andMe briefly split its service into three products—an Ancestry Edition, a Health Edition, and a Complete Edition—but recombined them a year later. A monthly subscription for research-based updates, introduced in late 2010, proved unpopular and was eliminated in mid-2012.

From November 22, 2013, to October 21, 2015, 23andMe sold only raw genetic data and ancestry-related results in the US due to FDA restrictions, after which it resumed providing health information in the form of carrier status and wellness reports.

Pricing

The US price declined from $999 at launch in 2007 to $399 in 2008 and to $99 in 2012, effectively serving as a loss leader to build the customer database. In October 2015, the price was raised to $199. In September 2016, an ancestry-only version was reintroduced at $99 with an optional $125 health upgrade. The product launched in Canada in October 2014 at CA$99 and in the United Kingdom in December 2014 at £125.

Ancestry and diversity initiatives

In February 2018, 23andMe enhanced its ancestry reporting to provide country-level rather than region-level estimates, adding 120 new regions. Acknowledging gaps in genomic data for Asia and Africa, the company launched the African Genetics Program in October 2016 (supported by a National Institutes of Health grant) to recruit sub-Saharan African participants. This was expanded into the Global Genetics Program in February 2018, targeting 61 underrepresented countries, and the Populations Collaboration Program in April 2018, establishing formal research partnerships.

23andMe+ and Lemonaid Health

In October 2020, 23andMe launched "23andMe+", a subscription service priced at $29 per year, offering additional health and pharmacogenetic reports to Health + Ancestry customers genotyped on version 5 of its microarray chip. In late 2021, the company completed its $400 million acquisition of Lemonaid Health, a telehealth company.

2023 data breach

In October 2023, a significant data breach was disclosed. Hackers accessed data on approximately 6.9 million users—roughly half of 23andMe's customers at the time—through a credential stuffing attack. Stolen data included names, addresses, and genetic information, and was subsequently offered for sale online. The affected accounts had enabled the platform's "DNA Relatives" feature, and the attack specifically targeted Ashkenazi Jewish and Chinese-descent users.

In June 2025, the UK's Information Commissioner's Office (ICO) fined 23andMe £2.31 million for failing to adequately protect user data, citing inadequate security measures—including the absence of multi-factor authentication—and a slow response to the breach.

In May 2026, the California Attorney General filed a lawsuit against 23andMe for failure to safeguard sensitive personal information under the California Consumer Privacy Act (CCPA) and other related privacy statutes.

From Wikipedia’s article on 23andMe, shared under CC BY-SA 4.0.9

Leadership

Who has led Chrome Holding Co., and when. Pick a name to see everywhere that person has worked.

Board members and other officers (23)

Products and brands

  • genetic testing

Listed on Wikidata.1

Technology

23andMe began offering direct-to-consumer genetic testing in November 2007. Customers submit a saliva sample from which DNA is extracted and amplified. The amplified DNA is applied to a glass microarray chip manufactured by Illumina, which contains microscopic beads, each bearing a gene probe complementary to a specific genetic variant. Where the customer's DNA matches a probe, the sequences hybridise and a fluorescent label indicates the variant is present. The platform tests hundreds of thousands of variants out of the approximately 10 to 30 million present in the human genome, and the results are compiled into reports informing the customer about variants associated with conditions such as Parkinson's disease, celiac disease, and Alzheimer's disease. In 2008, when the company was offering estimates of predisposition for more than 90 traits and conditions, Time magazine named the product "Invention of the Year".

Customers can download their uninterpreted raw genetic data and view results by chromosome, including mitochondrial DNA, to compare their variants with common population frequencies. Ancestry customers have access to genealogical DNA test tools, including a relative-matching database, and can view their mitochondrial haplogroup (maternal lineage) and, if male or if a patrilineal relative has been tested, their Y chromosome haplogroup (paternal lineage). US customers who received health-related results before November 22, 2013, retain online access to assessments of inherited traits and genetic disorder risks. Health-related results for US customers who purchased the test from November 22, 2013, were suspended until late 2015 while undergoing FDA regulatory review. Customers in Canada and the United Kingdom have access to some, but not all, health-related results.

23andMe is commonly used by donor-conceived people to find biological siblings and, in some cases, their sperm donor or egg donor.

Instrument and chip versions

Until 2010, Illumina sold its genotyping instruments labelled "for research use only"; in early 2010, Illumina obtained FDA approval for its BeadXpress system for clinical use.

Read the full text

Research

Overview

Over 80% of 23andMe customers have opted in to having their data used for research. The company's research programme has produced hundreds of peer-reviewed publications using its large genotyped and phenotyped participant database. Aggregated customer data is studied by researchers employed by 23andMe and through collaborations with academic, government, and pharmaceutical partners; de-identified customer data has also been licensed to pharmaceutical and biotechnology companies. In July 2012, 23andMe acquired CureTogether, a crowdsourced treatment ratings startup with data on over 600 medical conditions.

23andMe offers an optional consent allowing individual genetic information to be included in research published in scientific journals. However, even without this consent, de-identified genetic and self-reported data may be shared with the company's third-party service providers.

Parkinson's disease

In 2010, 23andMe reported using its database to validate NIH-published work identifying mutations in the glucocerebrosidase gene as a risk factor for Parkinson's disease. In 2015, the company began pursuing in-house drug discovery under former Genentech executive Richard Scheller, with Parkinson's disease as a primary focus.

Inflammatory bowel disease

23andMe established research agreements with Pfizer to investigate the genetic basis of inflammatory bowel disease, including ulcerative colitis and Crohn's disease.

Depression and psychiatric disorders

In 2016, 23andMe used self-reported customer data to identify 17 genetic loci associated with depression. In 2017, the company began collaborations with Lundbeck and the Milken Institute focusing on the genetics of bipolar disorder and major depression, with aims of advancing drug discovery.

COVID-19

In June 2020, 23andMe published preliminary results suggesting that people with type O blood may be at lower risk of COVID-19 infection. Among more than 750,000 participants, those with type O blood were 9–18% less likely to contract the virus, and those who had been exposed were 13–26% less likely to test positive. The study was published in April 2021 in Nature Genetics. Subsequent research examined genetic associations with COVID-19 symptoms such as loss of taste or smell, vaccine reactions across different ethnicities, and risk factors for long COVID. Findings on long COVID were presented at the 2023 ASHG conference.

Pharmacogenomics

In 2026, the 23andMe Research Institute published a genome-wide association study in Nature identifying genetic variants associated with variation in weight loss and side effects among users of GLP-1 receptor agonist medications.

Other research

In 2016, a project to offer customers next-generation sequencing was ended; Wojcicki cited concerns that results would be too complex for direct-to-consumer presentation.

From Wikipedia’s article on 23andMe, shared under CC BY-SA 4.0.9

Subsidiaries and ownership

Subsidiaries (Exhibit 21)

  • 23andMe Pharmacy Holdings, Inc. Delaware10
  • 23andMe, Inc. Delaware10
  • LPRXOne LLC Missouri10
  • LPRXThree LLC Missouri10
  • LPRXTwo LLC Missouri10
  • LPharm CS LLC Delaware10
  • LPharm INS LLC Delaware10
  • LPharm RX LLC Delaware10
  • Lemonaid Community Pharmacy Missouri10
  • Lemonaid Health Inc. Delaware10
  • Lemonaid Pharmacy Holdings, Inc. Delaware10

The subsidiaries the company lists in Exhibit 21 of its annual report, as filed.

Former names

  • 23andMe Holding Co.Jun 21, 2021 to Aug 4, 20258
  • 23andMe Holding CoJun 17, 2021 to Aug 14, 20251
  • VG Acquisition Corp.Sep 16, 2020 to Jun 17, 20218
  • Bleecker Street Acquisition Corp.Mar 6, 2020 to Aug 12, 20208
  • 23andMe, Inc.until Jun 16, 20211

Timeline

  1. Dec 4, 20258-K Bankruptcy or receivership46
  2. Nov 17, 20258-K Other events47
  3. Nov 4, 20258-K Regulation FD disclosure48
  4. Oct 6, 20258-K Regulation FD disclosure49
  5. Oct 1, 20258-K Other events50
  6. Sep 22, 20258-K Regulation FD disclosure51
  7. Sep 11, 20258-K Entered a material agreement52
  8. Aug 22, 20258-K Executive or director change53
  9. Aug 18, 20258-K Regulation FD disclosure54
  10. Aug 15, 20258-K Bylaws or fiscal year changed55
  11. Aug 14, 2025Renamed Name changed to Chrome Holding Co.1
  12. Jul 14, 20258-K Ended a material agreement; Completed an acquisition or sale; Other events56
  13. Jun 30, 20258-K Other events57
  14. May 21, 2025New chief executive Joseph Anthony Selsavage becomes CEO20
  15. Jun 17, 2021Went public Listed on NASDAQ1
  16. Oct 1, 2020New chief executive Joshua Bayliss becomes CEO21
  17. Apr 2006Founded Founded1
  18. 2006New chief executive Anne Wojcicki becomes CEO1

Calendar

When it reported results

  1. Jan 28, 2025Reported quarterly or annual results58
  2. Nov 12, 2024Reported quarterly or annual results59
  3. Aug 8, 2024Reported quarterly or annual results60
  4. May 23, 2024Reported quarterly or annual results61
  5. Feb 7, 2024Reported quarterly or annual results62
  6. Nov 8, 2023Reported quarterly or annual results63
  7. Aug 8, 2023Reported quarterly or annual results64
  8. May 25, 2023Reported quarterly or annual results65

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar

Filings

338 filings to the SEC since October 2021: 6 annual reports, 12 quarterly reports, 79 major events, 127 insider forms, 40 large holders, 74 other. The latest 20:

  1. Dec 4, 202515-12G EDGAR
  2. Dec 4, 20258-K EDGAR
  3. Nov 17, 20258-K EDGAR
  4. Nov 7, 2025NT 10-Q EDGAR
  5. Nov 4, 20258-K EDGAR
  6. Oct 6, 20258-K EDGAR
  7. Oct 1, 20258-K EDGAR
  8. Sep 22, 20258-K EDGAR
  9. Sep 11, 20258-K EDGAR
  10. Aug 22, 20258-K EDGAR
  11. Aug 21, 20254 EDGAR
  12. Aug 18, 20258-K EDGAR
  13. Aug 15, 20258-K EDGAR
  14. Aug 4, 202510-Q EDGAR
  15. Jul 25, 202510-K/A EDGAR
  16. Jul 14, 20258-K EDGAR
  17. Jun 30, 20258-K EDGAR
  18. Jun 20, 2025SCHEDULE 13G EDGAR
  19. Jun 16, 20258-K EDGAR
  20. Jun 16, 2025SCHEDULE 13D/A EDGAR

The 338 filings since October 2021 can be filtered by form type and year here when JavaScript is on.

Every filing from the last five years, summarized. The full record is on SEC EDGAR.

Insider trades

28 open-market trades by officers, directors and large owners since October 2021: 1 buys and 27 sales. Grants, option exercises and gifts are left out.

DateWhoTradeSharesPriceValueFiling
May 2, 2024HIBBS KATHY LChief Administrative OfficerSale38,551$0.49$18.9KForm 4
Apr 18, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.47$18.1KForm 4
Apr 4, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.50$19.3KForm 4
Mar 21, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.46$17.7KForm 4
Mar 7, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.53$20.4KForm 4
Feb 22, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.61$23.5KForm 4
Feb 15, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.78$30.1KForm 4
Jan 25, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.73$28.1KForm 4
Jan 11, 2024HIBBS KATHY LChief Administrative OfficerSale38,548$0.72$27.8KForm 4
Dec 28, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.93$35.9KForm 4
Dec 14, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.97$37.4KForm 4
Nov 30, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.88$33.9KForm 4
Nov 16, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.77$29.7KForm 4
Nov 2, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.87$33.5KForm 4
Oct 19, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.81$31.2KForm 4
Oct 5, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$0.84$32.4KForm 4
Sep 21, 2023HIBBS KATHY LChief Administrative OfficerSale38,548$1.00$38.5KForm 4
Sep 7, 2023HIBBS KATHY LChief Administrative OfficerSale40,894$1.06$43.3KForm 4
Sep 5, 2023Richards William GHead of Therapeutics DiscoverySale2,538$1.08$2.7KForm 4
Aug 24, 2023HIBBS KATHY LChief Administrative OfficerSale40,894$1.05$42.9KForm 4

All 28 trades can be filtered by person here when JavaScript is on.

From Forms 4 filed with the SEC.

Major holders

Investors who own more than 5% of the shares must tell the SEC: a 13D if they may seek to influence the company, a 13G if they hold passively.

SEC filer profile

How Chrome Holding Co. is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARChrome Holding Co.2
  • CIK0001804591
  • Employer ID (EIN)87-124034419
  • Filer statusAccelerated filer not an emerging growth company; not a smaller reporting company; not a shell company19
  • Incorporated inDelaware19
  • Fiscal year endsMarch 312
  • Industry code (SIC)2834 Pharmaceutical Preparations2
  • SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance2
  • Business address870 Market Street, Room 415, San Francisco, CA 941022
  • Phone(650) 938-63002
  • Shares outstanding20,499,552 Common Class A shares; 7,041,942 Common Class B shares as of May 31, 202519
  • Public float$120.3M as of Sep 30, 202419
  • AuditorKPMG LLP, Santa Clara, California PCAOB ID 185; it also attests to the company’s internal control over financial reporting19
  • On EDGAR sinceMar 6, 20202
  • Filings458 in all: 4 (128), 8-K (93), 3 (31), 424B3 (22), 144 (18), 10-Q (15), 425 (13), SC 13G (12)2
    All 49 form types

    SC 13G/A (12), CORRESP (10), SC 13D/A (10), SCHEDULE 13D/A (8), UPLOAD (8), EFFECT (6), S-8 (6), S-8 POS (6), 10-K (5), DEFA14A (4), 10-K/A (3), 4/A (3), 8-K/A (3), DEF 14A (3), 25 (2), 8-A12B (2), ARS (2), CERT (2), DEFR14A (2), DRS (2), NT 10-Q (2), POS AM (2), S-1 (2), S-4/A (2), SC 13D (2), SCHEDULE 13G/A (2), 15-12B (1), 15-12G (1), 25-NSE (1), 424B4 (1), DEFM14A (1), DRS/A (1), DRSLTR (1), PRE 14A (1), RW (1), S-1/A (1), S-1MEF (1), S-3 (1), S-4 (1), SCHEDULE 13D (1), SCHEDULE 13G (1)

  • Latest filingsAnnual report (10-K) Jun 11, 2025
    Quarterly report (10-Q) Aug 4, 2025
    Proxy statement (DEF 14A) Jul 16, 2024
    Latest 8-K (8-K) Dec 4, 2025

Securities registered for trading

ClassSymbolExchange
Class A common stock, $0.0001 par value per share

From the cover page of the 10-K filed Jun 11, 2025 (Section 12(b) of the Exchange Act).19

Risk factors and legal proceedings

The risks Chrome Holding Co. names in Item 1A of its 10-K filed Jun 11, 2025: 73 risks under these headings, as written.19

  • Unless the context indicates otherwise, references in this “Risk Factors” section to the “Company,” “we,” “us,” “our,” and similar terms refer to 23andMe Holding Co., a Delaware corporation formerly known as VG Acquisition Corp., and its consolidated subsidiaries.
  • Risks Related to Bankruptcy Proceedings
  • We are subject to risks and uncertainties associated with our Chapter 11 Cases.
  • As a result of our Chapter 11 Cases, our Class A common stock has and may continue to decrease in value and may eventually be rendered worthless.
  • Our Class A common stock has been delisted from Nasdaq and there is no guarantee that our Class A common stock will be regularly traded on the over-the-counter markets.
  • As a result of our Chapter 11 Cases, our financial results may be volatile and may not reflect historical trends.
  • Delays in our Chapter 11 Cases increase the risks of us being unable to sell substantially all of our assets or reorganize or liquidate our business and increase our costs associated with the bankruptcy process.
  • The DIP Facility has substantial restrictions and covenants and if we are unable to comply with the covenant requirements under the DIP Facility, it could have a material adverse impact on our financial condition, operating results and cash flows.
  • Our liquidity requirements and the adequacy of our capital resources are difficult to predict at this time.
  • Matters relating to Chapter 11 Cases have consumed and will continue to consume a substantial portion of the time and attention of our management, which may have an adverse effect on our business, and we may experience increased levels of employee attrition.
  • We may not be able to obtain confirmation of a Chapter 11 plan of reorganization or plan of liquidation or complete any Bankruptcy Court-approved sales of our Company or assets, including the Transaction.
  • In certain instances, a Chapter 11 case may be converted to a case under Chapter 7 of the Bankruptcy Code, in which case our common stock would likely be worthless.
The other 62 risks
  • The Chapter 11 Cases and the covenants in the Asset Purchase Agreement limit the flexibility of our management team in running our business.
  • Risks Related to Our Business
  • Business Risks Related to Products and Services
  • The market for personal genetics products and services has experienced a recent overall decline, which corresponds with the recent and significant decreases in our revenues. If this trend continues or worsens, it could adversely affect our business and results of operations.
  • We operate in highly competitive markets, and competition in the personal genetics and telehealth markets present an ongoing threat to the success of our business.
  • If our competitors receive further FDA marketing authorization for in vitro diagnostic products, our business could be adversely affected.
  • The sizes of the markets and forecasts of market growth for the demand of our products and services, including our research services and other key potential success factors, are based on a number of complex assumptions and estimates, and may be inaccurate.
  • Substantially all of our research services revenues were generated from the original GSK Agreement, and if we are unable to enter into additional collaboration agreements, our future research services revenue will decline.
  • The telehealth market is maturing and volatile, and if it does not develop, if it encounters negative publicity, or if the use of telehealth solutions does not continue to increase, then the growth of our business and our results of operation could be adversely affected.
  • We rely on key sole suppliers to manufacture and perform services used by customers who purchase our PGS. Our reliance on limited contracted manufacturing and supply chain capacity could adversely affect our ability to meet customer demand.
  • Changes to U.S. or other countries’ trade policies and tariff and import/export regulations or our failure to comply with such regulations may have an adverse effect on our business, financial condition, and results of operations.
  • Our business significantly depends upon the strength of our brands, and if we are not able to maintain and enhance our brand, our ability to expand our customer base may be impaired and our business and operating results may be harmed.
  • We have a limited history introducing new products and services to our customers and patients. If our efforts to attract new customers and patients and engage existing customers and patients with enhanced products and services are unsuccessful or if such efforts are more costly than we expect, our business may be harmed.
  • Revenue derived from our kit sales is dependent on seasonal holiday demand and the timing of Amazon Prime Day, which could lead to significant quarterly fluctuations in revenue and results of operations.
  • Our ability to meet demand in the Amazon retail channel is dependent upon Amazon’s stocking policies.
  • We have limited operating experience abroad and may be subject to increased business and economic risks that could impact our financial results.
  • Our pricing strategies may not meet customers’ price expectations or may adversely affect our revenues.
  • We depend on our relationships with the PMCs, which we do not own, to provide telehealth consultation services, and our business could be adversely affected if those relationships were disrupted.
  • We depend on a number of other companies to perform functions critical to our ability to operate our platform and generate revenue from patients.
  • If we are unable to attract and retain high quality healthcare providers for our patients, our business, financial condition, and results of operations may be materially and adversely affected.
  • Any significant disruption in service on our website, mobile applications, or in our computer or logistics systems, whether due to a failure with our information technology systems or that of a third-party vendor, could harm our reputation and may result in a loss of customers.
  • If we are unable to deliver a rewarding experience on mobile devices, whether through our mobile website or our mobile application, we may be unable to attract and retain customers and patients.
  • Use of social media and email may adversely affect our reputation or subject us to fines or other penalties.
  • Our success depends, in large part, on our ability to extend our presence in the personal genetics market, provide customers with a high level of service at a competitive price, achieve sufficient sales volume to realize economies of scale, and create innovative new features, products, and services to offer to our customers. Our failure to achieve any of these outcomes would adversely affect our business.
  • Our business relies on the continual growth of our database of information provided by customers who consent to participate in our research. If the number of our customers consenting to participate in our research programs declines or fails to grow, our research services revenue may be adversely affected, and our database may become less effective in facilitating our ability to create new features, products and services to offer to our customers.
  • Our business requires us to continue to improve and develop new data mining technologies and innovations in the use of genotypic and phenotypic data.
  • Media reports have reported on consumer data privacy and security concerns and the use of genetic information accessed from other genetic databases by law enforcement and governmental agencies. These reports may decrease the overall consumer demand for personal genetic products and services, including ours.
  • General Business Risks
  • We have experienced a criminal cyber incident and could in the future experience other security breaches, disruption to our business, or reputational harm.
  • We may be subject to legal proceedings and litigation, which are costly to defend and could materially harm our business and results of operations.
  • Our business and future operating results may be adversely affected by catastrophic or other events outside of our control.
  • Economic uncertainty or downturns, particularly affecting the markets and industries in which we operate, and on discretionary consumer spending could adversely affect our business, financial condition, and results of operations.
  • Impairment in the value of our intangible assets could have a material adverse effect on our operating results and financial condition.
  • The development and use of artificial intelligence or AI presents risks and challenges that can impact our business including by posing security risks to our confidential information, proprietary information, and personal data and could give rise to legal and/or regulatory actions, damage our reputation or otherwise materially harm our business.
  • Our strategic restructuring and the associated headcount reduction have significantly changed our business, resulted in significant expenses, may not result in anticipated savings, and has and will continue to disrupt our business.
  • Risks Related to Governmental Regulation
  • Our products and services are subject to extensive regulation by various U.S. federal and state agencies and equivalent foreign agencies and compliance with existing or future regulations could result in unanticipated sanctions, civil penalties, contractual damages, reputational harm, expenses, or limit our ability to offer our products and services.
  • We will face legal, reputational, and financial risks if we fail to protect our customer data from security breaches or cyberattacks. Changes in laws or regulations relating to privacy or the protection or transfer of data relating to individuals or genetic information, or any actual or perceived failure by us to comply with such laws and regulations or any other obligations relating to privacy or the protection or transfer of data relating to individuals, could adversely affect our business.
  • We have operations abroad where we have limited operating experience, and we may be subject to increased regulatory risks and local competition in the future.
  • Government regulation of healthcare creates risks and challenges with respect to our compliance efforts and our business strategies, and if we fail to comply with applicable healthcare and other governmental regulations, we could face substantial penalties, our business, financial condition, and results of operations could be adversely affected, and we may be required to restructure our operations.
  • As part of our telehealth business, we provide pharmacy and prescription medication services, which subjects us to additional healthcare laws and regulations and increases the complexity and extent of our compliance and regulatory obligations.
  • As part of our telehealth business, third parties may provide patients with compounded medications prescribed by our telehealth providers. If such third parties are not able to provide patients with compounded medications or if such third parties are not able to comply with FDA and state requirements, our telehealth business may be harmed.
  • Congress may provide the U.S. Food and Drug Administration (“FDA”) authority to regulate laboratory-developed tests (“LDTs”), or the FDA may appeal the court’s decision and restore its authority to regulate LDTs, each of which could result in increased costs and the imposition of fines or penalties, and could have a material adverse effect upon our business.
  • Although we discontinued our Therapeutics operating segment in November 2024, we may still be subject to ongoing risks relating to its activities.
  • Risks Related to Intellectual Property
  • If we lose our protection, through expiration or otherwise, or are unable to protect our IP, the value of our brands and other intangible assets may be diminished, and our business may be adversely affected.
  • Litigation with respect to our IP rights or our commercial activities could result in unanticipated expenses and, if resolved unfavorably, could harm our business.
  • We may not be able to protect our IP rights throughout the world.
  • Changes in patent law in the U.S. and other jurisdictions could diminish the value of patents in general, thereby impairing our ability to protect our products and services.
  • Issued patents covering our products and services could be found invalid or unenforceable if challenged.
  • We may be subject to claims that our employees, consultants, or independent contractors have wrongfully used or disclosed confidential information of third parties or that our employees have wrongfully used or disclosed alleged trade secrets of their former employers.
  • We may not be able to protect and enforce our trademarks.
  • We may be subject to claims challenging the inventorship or ownership of our patents and other IP.
  • If we become involved in patent litigation or other proceedings related to a determination of rights, we could incur substantial costs and expenses, substantial liability for damages or be required to stop our development and commercialization efforts of our products and services.
  • Patent terms may be inadequate to protect our competitive position on our products and services for an adequate amount of time.
  • We utilize open-source software, which may pose particular risks to our proprietary software and source code.
  • Risks Related to Financial Reporting and Results of Operations
  • If we fail to maintain effective internal control over financial reporting or experience material weaknesses in the future, our ability to produce timely and accurate financial statements could be impaired, which may adversely affect our business.
  • Our quarterly operating results may fluctuate significantly.
  • Our ability to use our net operating loss carryforwards may be subject to limitations.
  • We have incurred significant losses since inception, we expect to incur losses in the future, and we may not be able to generate sufficient revenue to achieve and maintain profitability.
  • Our reported financial results may be adversely affected by changes in accounting principles generally accepted in the U.S.
  • We are subject to changing law and regulations regarding regulatory matters, corporate governance, and public disclosure that have increased our costs and the risk of non-compliance.
  • There is substantial doubt regarding our ability to continue as a going concern.
  • Risks Related to Ownership of Our Class A Common Stock
  • Our Certificate of Incorporation designates a state or federal court located within the State of Delaware as the sole and exclusive forum for substantially all disputes between us and our stockholders, which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us or our directors, officers, stockholders, employees, or agents. Our Second Amended and Restated Bylaws designate the United States federal district courts as the exclusive forum for the resolution of actions asserting claims arising under the Securities Act of 1933, as amended.
  • The dual class structure of our common stock may limit stockholders’ ability to influence the outcome of important decisions.
  • The ultimate effect of the Reverse Stock Split on the market price of our Class A common stock cannot be predicted with any certainty and may decrease the liquidity of our Class A common stock and magnify any decrease in our overall market capitalization.

Legal proceedings

For a discussion of our Chapter 11 Cases and legal proceedings, refer to Note 3, “Bankruptcy Proceedings,” and Note 13, “Commitments and Contingencies,” respectively, to our consolidated financial statements included elsewhere in this Form 10-K.

As a result of the Chapter 11 Cases, substantially all proceedings pending against us have been stayed.

The opening of Item 3, Legal Proceedings.19

Sources

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