Private company

Sonnet BioTherapeutics Holdings, Inc.

Sonnet BioTherapeutics Holdings, Inc. is an American pharmaceutical preparations company based in Princeton.1

Last updated Oct 20, 2026.

Overview

$1.0MRevenue, fiscal 20252
-$16.0MNet income, fiscal 20252
  • IndustryPharmaceutical Preparations1
  • HeadquartersPrinceton, New Jersey1
  • Incorporated inDE3
  • Business address100 Overlook Center, Suite 102, Princeton, Nj 085403
  • Filer categoryNon-accelerated filer, Smaller reporting company3
  • Legal formCorporation

(SOC) for PROC in a randomized comparison to show proof-of-concept (POC) in a larger population.4 From its latest annual report

Financials

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

Key numbers, fiscal 2025

-1584.4%Operating margin2
-1601.1%Net margin2
5268.8%Revenue growth, 20252
-148.4%Return on equity2

Where the money goes

Where each dollar of revenue went, fiscal 2025

  • Research and development97¢$8.4M
  • Income tax3¢$218.4K

Out of $1.0M in revenue.2 The company lost money this year.

Financial statements

Revenue56782$1.0M in 2025−97% since 2018
0$10.0M$20.0M$30.0M$40.0M2018: $30.7M$30.7M20182019: $30.1M$30.1M2019−2%2021: $483.6K$483.6K2021−98%2022: $349.9K$349.9K2022−28%2023: $147.8K$147.8K2023−58%2024: $18.6K$18.6K2024−87%2025: $1.0M$1.0M2025+5269%
Operating income596782-$15.8M in 2025+195% since 2018
-$30.0M-$20.0M-$10.0M02018: -$5.4M-$5.4M20182019: -$16.1M-$16.1M2019+199%2020: -$24.2M-$24.2M2020+51%2021: -$25.1M-$25.1M2021+4%2022: -$29.7M-$29.7M2022+18%2023: -$18.8M-$18.8M2023−37%2024: -$11.8M-$11.8M2024−37%2025: -$15.8M-$15.8M2025+34%
Net income596782-$16.0M in 2025+134% since 2018
-$30.0M-$20.0M-$10.0M02018: -$6.9M-$6.9M20182019: -$17.7M-$17.7M2019+159%2020: -$24.3M-$24.3M2020+37%2021: -$25.0M-$25.0M2021+3%2022: -$29.7M-$29.7M2022+19%2023: -$18.8M-$18.8M2023−37%2024: -$7.4M-$7.4M2024−61%2025: -$16.0M-$16.0M2025+115%
Fiscal year20182019202020212022202320242025
Revenue$30.7M5$30.1M5$483.6K6$349.9K7$147.8K8$18.6K2$1.0M2
Research and development$2.2M12$9.9M12$16.6M6$21.4M7$11.8M8$5.7M2$8.4M2
Operating expenses$30.0M7$18.9M8$11.9M2$16.8M2
Operating income-$5.4M5-$16.1M5-$24.2M9-$25.1M6-$29.7M7-$18.8M8-$11.8M2-$15.8M2
Interest$2.5M5$673.6K5
Income before tax-$7.4M2-$15.8M2
Income tax-$701.2K5$73.7K5$218.4K2
Net income-$6.9M5-$17.7M5-$24.3M9-$25.0M6-$29.7M7-$18.8M8-$7.4M2-$16.0M2
Earnings per share-$14.256-$150.527-$145.138-$11.352-$3.952
Earnings per share (diluted)-$150.527-$145.138-$11.352-$3.952
Shares (weighted, basic)197.5K shares7129.8K shares8655.2K shares24.1M shares2
Shares (weighted, diluted)197.5K shares7129.8K shares8655.2K shares24.1M shares2

Compare Sonnet BioTherapeutics Holdings, Inc. with another company

Corporate structure

Sonnet BioTherapeutics Holdings, Inc. sits at the top of its group. 1 entity, 1 country on record. Switch between the flow chart and the network, and select any entity to see its details.

Major holders of Sonnet BioTherapeutics Holdings, Inc.

  • Republic Digital Opportunistic Digital Assets Master Fund, Ltd. Filed SCHEDULE 13G on Sonnet BioTherapeutics Holdings, Inc., latest Jul 25, 2025
  • John Markey Filed SC 13G/A on Sonnet BioTherapeutics Holdings, Inc., latest Jan 2, 2024 (11 filings since May 2, 2023)
  • Matthew J. Ruck Filed SC 13G/A on Sonnet BioTherapeutics Holdings, Inc., latest Jun 22, 2023 (4 filings since Jun 9, 2023)
  • Hudson Bay Capital Management LP Filed SC 13G/A on Sonnet BioTherapeutics Holdings, Inc., latest Feb 10, 2023 (2 filings since Feb 3, 2022)
  • Sonnet BioTherapeutics Holdings, Inc. Princeton, New Jersey

Built from major holders from Schedules 13D and 13G. Each entity in the chart links to its source.

What it owns

What Sonnet BioTherapeutics Holdings, Inc. 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
Property and equipment, net$10.9K2 Sep 30, 2025$20.5K2 Sep 30, 2024−46.9%
Operating-lease assets (leased space)$43.8K2 Sep 30, 2025$123.4K2 Sep 30, 2024−64.5%

Investments

ItemLatestA year beforeChange
Cash and cash equivalents$5.1M2 Sep 30, 2025$149.5K2 Sep 30, 2024+3325.9%

Properties, in its own words

The Company relies on short term office use contracts to procure office and meeting space.

Item 2 of the 10-K filed Dec 16, 2025.4

Leadership

Who has led Sonnet BioTherapeutics Holdings, Inc., and when. Pick a name to see everywhere that person has worked.

Board members and other officers (24)

Named in SEC Form D filings

People the company listed in its private-offering notices.

  • Executive OfficerJay Cross named Aug 19, 2022 to Dec 23, 202449
  • Executive OfficerRichard K. Kenny named Aug 19, 2022 to Dec 23, 202449
  • DirectorLori K. McNeil named Dec 23, 202449

Former names

  • Chanticleer Holdings, Inc.May 10, 2005 to Mar 31, 20203
  • TULVINE SYSTEMS INCMar 7, 2000 to Mar 31, 20053

Timeline

  1. Dec 3, 20258-K Completed an acquisition or sale; Listing notice or transfer; Unregistered sale of shares50
  2. Dec 2, 20258-K Other events51
  3. Nov 18, 20258-K Regulation FD disclosure52
  4. Sep 29, 20258-K Shareholder vote53
  5. Aug 1, 20258-K Executive or director change54
  6. Jul 25, 20258-K Other events55
  7. Jul 18, 20258-K Other events56
  8. Jul 15, 2025New chief executive Raghu Rao becomes CEO15
  9. Jul 14, 20258-K Entered a material agreement; Unregistered sale of shares; Executive or director change57
  10. Jul 2, 20258-K Entered a material agreement; New debt or obligation; Unregistered sale of shares58
  11. Jun 2, 20258-K Listing notice or transfer; Other events59
  12. Apr 4, 20258-K Other events60
  13. Apr 1, 20258-K Executive or director change61
  14. Apr 3, 2020New chief executive Pankaj Mohan becomes CEO16
  15. Jan 18, 2006New chief executive Michael D. Pruitt becomes CEO17

Calendar

When it reported results

  1. Feb 13, 2025Reported quarterly or annual results62
  2. Dec 17, 2024Reported quarterly or annual results63
  3. Aug 14, 2024Reported quarterly or annual results64
  4. May 14, 2024Reported quarterly or annual results65
  5. Feb 14, 2024Reported quarterly or annual results66
  6. Dec 14, 2023Reported quarterly or annual results67
  7. Aug 14, 2023Reported quarterly or annual results68
  8. May 10, 2023Reported quarterly or annual results69

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

Filings

353 filings to the SEC since October 2021: 6 annual reports, 12 quarterly reports, 89 major events, 62 insider forms, 18 large holders, 3 private raises, 163 other. The latest 20:

  1. Jul 17, 202610-K/A EDGAR
  2. Dec 16, 2025EFFECT EDGAR
  3. Dec 16, 2025EFFECT EDGAR
  4. Dec 16, 2025EFFECT EDGAR
  5. Dec 16, 2025EFFECT EDGAR
  6. Dec 16, 2025EFFECT EDGAR
  7. Dec 16, 2025EFFECT EDGAR
  8. Dec 16, 2025EFFECT EDGAR
  9. Dec 16, 2025EFFECT EDGAR
  10. Dec 16, 2025EFFECT EDGAR
  11. Dec 16, 2025EFFECT EDGAR
  12. Dec 16, 2025EFFECT EDGAR
  13. Dec 16, 2025EFFECT EDGAR
  14. Dec 16, 2025EFFECT EDGAR
  15. Dec 16, 2025EFFECT EDGAR
  16. Dec 16, 2025EFFECT EDGAR
  17. Dec 16, 2025EFFECT EDGAR
  18. Dec 16, 2025EFFECT EDGAR
  19. Dec 16, 2025EFFECT EDGAR
  20. Dec 16, 2025EFFECT EDGAR

The 353 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

7 open-market trades by officers, directors and large owners since October 2021: 7 buys and 0 sales. Grants, option exercises and gifts are left out.

DateWhoTradeSharesPriceValueFiling
Oct 27, 2023Rao RaghuChief Executive OfficerBuy15,625Form 4
Oct 27, 2023Mohan PankajChairman, President and CEOBuy34,375Form 4
Jun 14, 2023Dexter SusanDirectorBuy10,000$0.70$7.0KForm 4
May 30, 2023Dyrness Albert D.DirectorBuy23,255$0.47$10.9KForm 4
May 17, 2023Bhatt NaileshDirectorBuy25,000$0.23$5.8KForm 4
May 15, 2023Mohan PankajChairman, President and CEOBuy371,600$0.22$81.8KForm 4
Mar 15, 2023Mohan PankajChairman, President and CEOBuy60,000$0.59$35.4KForm 4

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.

Executive pay

What the company paid its top executives, from the summary compensation table in its proxy statement. Total pay includes salary, bonus, stock and option awards and other pay, as the company valued them.

YearExecutiveAgeSalaryTotal pay
2024Pankaj MohanPh.D.$539.0K$626.6K74
2024John CiniPh.D.$397.8K$419.7K74
2024Jay Cross$388.7K$406.8K74
2023President and Chief Executive Officer$539.0K$634.7K74
2023Chief Scientific Officer$397.8K$441.7K74
2023Chief Financial Officer$388.7K$404.6K74

Money raised

Private offerings the company reported to the SEC on Form D.

  1. Dec 10, 2024Raised $3.9 million in a private offering of equity Form D: 4 investors so far Form D
  2. Jun 30, 2023Raised $2.2 million in a private offering of equity Form D: 1 investor so far Form D
  3. Aug 15, 2022Raised $2.2 million in a private offering of equity Form D: 5 investors so far Form D

SEC filer profile

How Sonnet BioTherapeutics Holdings, Inc. is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARSonnet BioTherapeutics Holdings, Inc.1
  • CIK0001106838
  • Employer ID (EIN)20-29326524
  • Filer statusNon-accelerated filer not an emerging growth company; a smaller reporting company; a shell company4
  • Incorporated inDelaware4
  • Fiscal year endsSeptember 301
  • Industry code (SIC)2834 Pharmaceutical Preparations1
  • SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance1
  • Business address100 Overlook Center, Suite 102, Princeton, NJ 085401
  • Phone609-375-22271
  • Shares outstanding1 shares as of Dec 12, 20254
  • Public float$4.2M as of Mar 31, 20254
  • AuditorKPMG LLP, Philadelphia, Pennsylvania PCAOB ID 185; no auditor attestation of internal control over financial reporting4
  • On EDGAR sinceFeb 15, 20001
  • Filings1,216 in all: 8-K (294), 4 (222), CORRESP (67), 10-Q (61), EFFECT (59), UPLOAD (51), 3 (36), POS AM (33)1
    All 62 form types

    S-1/A (32), SC 13G/A (26), 10-K (21), 424B3 (20), SC 13G (19), 10QSB (16), DEF 14A (16), SC 13D/A (16), 10-K/A (14), 425 (14), 8-K/A (14), S-3 (14), 10-Q/A (13), S-1 (13), D (12), DEFA14A (10), 424B4 (9), 424B5 (9), PRE 14A (9), S-3/A (9), NT 10-K (8), FWP (6), NT 10-Q (6), S-8 (6), S-8 POS (6), 10KSB (5), 1-E (4), 2-E (4), 4/A (4), 10KSB/A (3), 25-NSE (3), 5 (3), ARS (3), SC 13D (3), 10SB12G/A (2), 3/A (2), PRE 14C (2), 10SB12G (1), 15-12G (1), 2-E/A (1), 40-17G (1), 424B2 (1), 8-A12B (1), AW (1), CERTNAS (1), DEF 14C (1), DEFM14A (1), N-54A (1), N-54C (1), PRER14A (1), PRER14C (1), S-4 (1), S-4/A (1), SCHEDULE 13G (1)

  • Latest filingsAnnual report (10-K) Dec 16, 2025
    Quarterly report (10-Q) Aug 13, 2025
    Proxy statement (DEF 14A) Aug 26, 2025
    Latest 8-K (8-K) Dec 3, 2025

Securities registered for trading

ClassSymbolExchange
Common Stock, $0.0001 par value per shareSONNNasdaq

From the cover page of the 10-K filed Dec 16, 2025 (Section 12(b) of the Exchange Act).4

Risk factors and legal proceedings

The risks Sonnet BioTherapeutics Holdings, Inc. names in Item 1A of its 10-K filed Dec 16, 2025: 60 risks under these headings, as written.4

  • Risks Related to Our Financial Position and Need for Additional Capital
  • We have a history of significant operating losses and expect to incur significant and increasing losses for the foreseeable future, and we may never achieve or maintain profitability.
  • Our limited operating history may make it difficult for you to evaluate the success of our business to date and to assess our future viability.
  • Our recurring losses from operations have raised substantial doubt regarding our ability to continue as a going concern.
  • We will need substantial additional funding, and if we are unable to raise capital when needed, we could be forced to delay, reduce or eliminate our product discovery and development programs or commercialization efforts.
  • Risks Related to the Discovery, Development and Regulatory Approval of Our Product Candidates
  • We are substantially dependent on the success of our internal development programs and our product pipeline candidates may not successfully complete clinical trials, receive regulatory approval or be successfully commercialized.
  • We are at an early stage in our development efforts, our product candidates represent a new category of medicines and may be subject to heightened regulatory scrutiny until they are established as a therapeutic modality.
  • Our product candidates and those of any collaborators will need to undergo preclinical and clinical trials that are time-consuming and expensive, the outcomes of which are unpredictable, and for which there is a high risk of failure. If preclinical or clinical trials of our or their product candidates fail to satisfactorily demonstrate safety and efficacy to the FDA, the EMA and any other comparable regulatory authority, additional costs may be incurred or delays experienced in completing, the development of these product candidates, or their development may be abandoned.
  • We may find it difficult to enroll patients in our clinical trials, which could delay or prevent us from proceeding with clinical trials of our product candidates.
  • Results of preclinical studies and early clinical trials may not be predictive of results of future clinical trials.
  • Our current or future product candidates may cause undesirable side effects or have other properties when used alone or in combination with other approved products or investigational new drugs that could halt their clinical development, prevent their marketing approval, limit their commercial potential or result in significant negative consequences.
The other 49 risks
  • We may not be successful in our efforts to identify or discover additional product candidates.
  • We may expend our limited resources to pursue a particular product candidate or indication and fail to capitalize on product candidates or indications that may be more profitable or for which there is a greater likelihood of success.
  • We face potential product liability, and, if successful claims are brought against us, we may incur substantial liability and costs. If the use of our product candidates harms patients, or is perceived to harm patients even when such harm is unrelated to our product candidates, our regulatory approvals could be revoked or otherwise negatively impacted and we could be subject to costly and damaging product liability claims.
  • We may seek designations for our product candidates with the FDA and other comparable regulatory authorities that are intended to confer benefits such as a faster development process or an accelerated regulatory pathway, but there can be no assurance that we will successfully obtain such designations. In addition, even if one or more of our product candidates are granted such designations, we may not be able to realize the intended benefits of such designations.
  • We may seek priority review designation for one or more of our product candidates, but we might not receive such designation, and even if we do, such designation may not lead to a faster regulatory review or approval process.
  • Obtaining and maintaining marketing approval of our current and future product candidates in one jurisdiction does not mean that we will be successful in obtaining marketing approval of our current and future product candidates in other jurisdictions.
  • The widespread outbreak of communicable diseases could materially and adversely affect our business, financial condition and results of operations.
  • Risks Related to Commercialization of Our Product Candidates and Other Regulatory Compliance Matters
  • Even if we complete the necessary preclinical studies and clinical trials, the marketing approval process is expensive, time consuming and uncertain and may prevent us or any collaborators from obtaining approvals for the commercialization of some or all of our product candidates. As a result, we cannot predict when or if, and in which territories, we, or any collaborators, will obtain marketing approval to commercialize a product candidate.
  • We currently have no marketing, sales or distribution infrastructure with respect to our product candidates. If we are unable to develop our sales, marketing and distribution capability on our own or through collaborations with marketing partners, we will not be successful in commercializing our product candidates.
  • The market opportunities for any current or future product candidate we develop, if and when approved, may be limited to those patients who are ineligible for established therapies or for whom prior therapies have failed, and therefore may be small.
  • Even if we receive marketing approval of a product candidate, we will be subject to ongoing regulatory obligations and continued regulatory review, which may result in significant additional expense and we may be subject to penalties if we fail to comply with regulatory requirements or experience unanticipated problems with our products, if approved.
  • We face significant competition and if our competitors develop and market products that are more effective, safer or less expensive than the product candidates we develop, our commercial opportunities will be negatively impacted.
  • The commercial success of any current or future product candidate will depend upon the degree of market acceptance by physicians, patients, payors and others in the medical community.
  • If the market opportunities for our product candidates are smaller than we believe they are, our product revenues may be adversely affected and our business may suffer.
  • The insurance coverage and reimbursement status of newly-approved products is uncertain. Failure to obtain or maintain adequate coverage and reimbursement for any of our product candidates, if approved, could limit our ability to market those products and decrease our ability to generate revenue.
  • If the FDA or comparable foreign regulatory authorities approve generic versions of any of our product candidates that receive marketing approval, or such authorities do not grant such products appropriate periods of data exclusivity before approving generic versions of such products, the sales of such products could be adversely affected.
  • We may be subject, directly or indirectly, to federal and state healthcare fraud and abuse laws, false claims laws health information privacy and security laws, and other health care laws and regulations. If we are unable to comply, or have not fully complied, with such laws, we could face substantial penalties.
  • Healthcare legislative reform measures and constraints on national budget social security systems may have a material adverse effect on our business and results of operations.
  • We are subject to the U.S. Foreign Corrupt Practices Act of 1977, as amended, or the FCPA, and other anti-corruption laws, as well as export control laws, import and customs laws, trade and economic sanctions laws and other laws governing our operations.
  • Recently enacted and future policies and legislation may increase the difficulty and cost for us to obtain marketing approval of and commercialize our product candidates and may affect the reimbursement made for any product candidate for which we receive marketing approval.
  • If we fail to comply with environmental, health and safety laws and regulations, we could become subject to fines or penalties or incur costs that could have a material adverse effect on the success of our business.
  • Risks Related to Our International Operations
  • As one of our subsidiaries, Relief, is based outside of the United States, we are subject to economic, political, regulatory and other risks associated with international operations.
  • European data collection is governed by restrictive regulations governing the use, processing, and cross-border transfer of personal information.
  • Risks Related to Our Dependence on Third Parties
  • For certain product candidates, we may depend on development and commercialization collaborators to develop and conduct clinical trials with, obtain regulatory approvals for, and if approved, market and sell product candidates. If such collaborators fail to perform as expected, the potential for us to generate future revenue from such product candidates would be significantly reduced and our business would be harmed.
  • If conflicts arise with our development and commercialization collaborators or licensors, they may act in their own self-interest, which may be adverse to the interests of our company.
  • We will rely on third parties, including independent clinical investigators and CROs, to conduct and sponsor some of the clinical trials of our product candidates. Any failure by a third party to meet its obligations with respect to the clinical development of our product candidates may delay or impair our ability to obtain regulatory approval for our product candidates.
  • We intend to rely on third parties to manufacture product candidates, which increases the risk that we will not have sufficient quantities of such product candidates or products or such quantities at an acceptable cost, which could delay, prevent or impair our development or commercialization efforts.
  • Our reliance on third parties requires us to share our trade secrets, which increases the possibility that a competitor will discover them or that our trade secrets will be misappropriated or disclosed.
  • Risks Related to Our Intellectual Property
  • If we are unable to obtain and maintain patent and other intellectual property protection for our products and product candidates, or if the scope of the patent and other intellectual property protection obtained is not sufficiently broad, our competitors could develop and commercialize products similar or identical to ours, and our ability to successfully commercialize our products and product candidates may be adversely affected.
  • Issued patents covering our products and product candidates could be found invalid or unenforceable if challenged in court or in administrative proceedings. We may not be able to protect our trade secrets in court.
  • We may be subject to claims challenging the inventorship or ownership of the patents and other intellectual property.
  • Obtaining and maintaining patent protection depends on compliance with various procedural, document submission, fee payment and other requirements imposed by governmental patent agencies, and our patent protection could be reduced or eliminated for non- compliance with these requirements.
  • If we do not obtain patent term extension and data exclusivity for our products and product candidates, our business may be materially harmed.
  • Changes in patent law in the United States and other jurisdictions could diminish the value of patents in general, thereby impairing our ability to protect our products and product candidates.
  • We may not be able to protect our intellectual property rights throughout the world.
  • If we are sued for infringing intellectual property rights of third parties, such litigation could be costly and time consuming and could prevent or delay us from developing or commercializing our product candidates.
  • We may be subject to claims by third parties asserting that our employees or we have misappropriated their intellectual property, or claiming ownership of what we regard as our own intellectual property.
  • We may become involved in lawsuits to protect or enforce our patents and other intellectual property rights, which could be expensive, time-consuming and unsuccessful.
  • If we fail to comply with our obligations under any future intellectual property licenses with third parties, we could lose license rights that are important to our business.
  • If our trademarks and trade names are not adequately protected, then we may not be able to build name recognition in our marks of interest and our business may be adversely affected.
  • Risks Related to Employee Matters and Managing Growth
  • We only have a limited number of employees to manage and operate our business.
  • Our future success depends on our ability to retain key employees, consultants and advisors and to attract, retain and motivate qualified personnel.
  • Our employees, independent contractors, consultants, collaborators and contract research organizations may engage in misconduct or other improper activities, including non-compliance with regulatory standards and requirements, which could cause significant liability for us and harm our reputation.
  • We expect to expand our organization, and as a result, we may encounter difficulties in managing our growth, which could disrupt our operations.
  • Risks Related to Our Common Stock
  • We incur significant costs and devote substantial management time as a result of operating as a public company, and we expect those costs to increase.
  • Director and officer liability is limited.
  • General Risk Factors
  • Cyber-attacks or other failures in telecommunications or information technology systems could result in information theft, data corruption and significant disruption of our business operations.
  • Our business, strategy, and access to capital may be adversely affected by the business, financial condition, and decisions of HSI.

Legal proceedings

We are not currently subject to any material legal proceedings. However, we may from time to time become a party to various legal proceedings arising in the ordinary course of our business.

The opening of Item 3, Legal Proceedings.4

Sources

The numbers on this page point here. Each one links to the record it came from.

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20
  21. 21
  22. 22
  23. 23
  24. 24
  25. 25
  26. 26
  27. 27
  28. 28
  29. 29
  30. 30
  31. 31
  32. 32
  33. 33
  34. 34
  35. 35
  36. 36
  37. 37
  38. 38
  39. 39
  40. 40
  41. 41
  42. 42
  43. 43
  44. 44
  45. 45
  46. 46
  47. 47
  48. 48
  49. 49
  50. 50
  51. 51
    SEC EDGAROther events
  52. 52
  53. 53
  54. 54
  55. 55
    SEC EDGAROther events
  56. 56
    SEC EDGAROther events
  57. 57
  58. 58
  59. 59
  60. 60
    SEC EDGAROther events
  61. 61
  62. 62
  63. 63
  64. 64
  65. 65
  66. 66
  67. 67
  68. 68
  69. 69
  70. 70
  71. 71
  72. 72
  73. 73
  74. 74