MLTX on Nasdaq
MoonLake Immunotherapeutics
In its 2026 annual report the company says: “We are a clinical stage biotechnology company advancing therapies to address significant unmet needs in inflammatory skin and joint diseases. We are currently a single asset company focused on the development of SLK, a novel tri-specific IL-17A and IL-17F inhibiting Nanobody, that we exclusively licensed from MHKDG and that has the potential, based on response levels seen in clinical trials, to drive disease modification in dermatology and rheumatology patients.”4 Its shares trade on Nasdaq under the symbol MLTX.1
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Last updated Oct 21, 2026.
Overview
- TickerMLTX on Nasdaq1
- IndustryPharmaceutical Preparations1
- HeadquartersE91
- Incorporated inCayman Islands3
- Business addressDorfstrasse 29, Zug, V8 63003
- Filer categoryLarge accelerated filer3
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We are a clinical stage biotechnology company advancing therapies to address significant unmet needs in inflammatory skin and joint diseases. We are currently a single asset company focused on the development of SLK, a novel tri-specific IL-17A and IL-17F inhibiting Nanobody, that we exclusively licensed from MHKDG and that has the potential, based on response levels seen in clinical trials, to drive disease modification in dermatology and rheumatology patients.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
Financial statements
Every line of the income statement as filed: the last 3 fiscal years, latest first.2
| Period ending | 2025-12-31 | 2024-12-31 | 2023-12-31 |
|---|---|---|---|
| Research and development | -$202.9M | -$112.8M | -$31.8M |
| General and administrative | -$42.0M | -$30.3M | -$22.3M |
| Total operating expenses | -$244.8M | -$143.1M | -$54.1M |
| Operating loss | -$244.8M | -$143.1M | -$54.1M |
| Interest expense | -$7.2M | $0 | $0 |
| Other income, net | $22.4M | $22.1M | $10.1M |
| Loss before income tax | -$229.7M | -$121.0M | -$44.0M |
| Income tax expense | -$611.0K | -$282.0K | -$94.0K |
| Net loss | -$230.3M | -$121.2M | -$44.1M |
| Of which: net loss attributable to controlling interests shareholders | -$227.3M | -$118.9M | -$36.0M |
| Of which: net loss attributable to noncontrolling interests shareholders | -$3.0M | -$2.3M | -$8.1M |
| Net unrealized gain (loss) on marketable securities and short-term investments | -$5.1M | $2.7M | $2.3M |
| Actuarial gain (loss) on employee benefit plans | $641.0K | -$87.0K | -$336.0K |
| Other comprehensive income (loss) | -$4.5M | $2.6M | $2.0M |
| Comprehensive loss | -$234.8M | -$118.6M | -$42.1M |
| Comprehensive loss attributable to controlling interests shareholders | -$231.7M | -$116.4M | -$34.5M |
| Comprehensive loss attributable to noncontrolling interests | -$3.1M | -$2.3M | -$7.6M |
| Weighted-average number of shares, basic (in shares) | 64.5M shares | 62.9M shares | 49.1M shares |
| Weighted-average number of shares, diluted (in shares) | 64.5M shares | 62.9M shares | 49.1M shares |
| Basic net loss per share attributable to controlling interest shareholders (USD per share) | -$3.53 | -$1.89 | -$0.73 |
| Diluted net loss per share attributable to controlling interest shareholders (USD per share) | -$3.53 | -$1.89 | -$0.73 |
No quarter-by-quarter statement was filed.
Every line of the balance sheet as filed: the last 4 fiscal years (annual) or 4 quarters (quarterly), latest first.2
| Period ending | 2025-12-31 | 2024-12-31 | 2023-12-31 | 2022-12-31 |
|---|---|---|---|---|
| Cash and cash equivalents | $334.5M | $180.4M | ||
| Short-term marketable debt securities | $59.5M | $267.6M | ||
| Other receivables | $4.9M | $2.8M | ||
| Prepaid expenses | $22.9M | $23.4M | ||
| Total current assets | $421.7M | $474.3M | ||
| Operating lease right-of-use assets | $1.6M | $2.9M | ||
| Property and equipment, net | $577.0K | $722.0K | ||
| Other non-current assets | $596.0K | $0 | ||
| Total non-current assets | $2.7M | $3.6M | ||
| Total assets | $424.4M | $477.9M | ||
| Trade and other payables | $29.6M | $9.0M | ||
| Accrued expenses and other current liabilities | $14.7M | $12.1M | ||
| Short-term portion of operating lease liabilities | $1.2M | $1.4M | ||
| Total current liabilities | $45.5M | $22.5M | ||
| Long-term debt | $74.1M | $0 | ||
| Long-term portion of operating lease liabilities | $374.0K | $1.5M | ||
| Pension liability | $0 | $621.0K | ||
| Total non-current liabilities | $74.5M | $2.1M | ||
| Total liabilities | $120.0M | $24.5M | ||
| Additional paid-in capital | $766.8M | $677.4M | ||
| Accumulated deficit | -$462.9M | -$235.6M | ||
| Accumulated other comprehensive income | $604.0K | $5.0M | ||
| Total shareholders equity | $304.5M | $446.8M | ||
| Noncontrolling interests | $0 | $6.6M | ||
| Total equity | $304.5M | $453.4M | $513.5M | $68.8M |
| Total liabilities and equity | $424.4M | $477.9M |
| Period ending | 2025-12-31 | 2024-12-31 | 2023-12-31 | 2022-12-31 |
|---|---|---|---|---|
| Cash and cash equivalents | $334.5M | $180.4M | ||
| Short-term marketable debt securities | $59.5M | $267.6M | ||
| Other receivables | $4.9M | $2.8M | ||
| Prepaid expenses | $22.9M | $23.4M | ||
| Total current assets | $421.7M | $474.3M | ||
| Operating lease right-of-use assets | $1.6M | $2.9M | ||
| Property and equipment, net | $577.0K | $722.0K | ||
| Other non-current assets | $596.0K | $0 | ||
| Total non-current assets | $2.7M | $3.6M | ||
| Total assets | $424.4M | $477.9M | ||
| Trade and other payables | $29.6M | $9.0M | ||
| Accrued expenses and other current liabilities | $14.7M | $12.1M | ||
| Short-term portion of operating lease liabilities | $1.2M | $1.4M | ||
| Total current liabilities | $45.5M | $22.5M | ||
| Long-term debt | $74.1M | $0 | ||
| Long-term portion of operating lease liabilities | $374.0K | $1.5M | ||
| Pension liability | $0 | $621.0K | ||
| Total non-current liabilities | $74.5M | $2.1M | ||
| Total liabilities | $120.0M | $24.5M | ||
| Additional paid-in capital | $766.8M | $677.4M | ||
| Accumulated deficit | -$462.9M | -$235.6M | ||
| Accumulated other comprehensive income | $604.0K | $5.0M | ||
| Total shareholders equity | $304.5M | $446.8M | ||
| Noncontrolling interests | $0 | $6.6M | ||
| Total equity | $304.5M | $453.4M | $513.5M | $68.8M |
| Total liabilities and equity | $424.4M | $477.9M |
Cash flow is reported year to date, not quarter by quarter, so there are no separate quarterly figures.
Every line of the cash flow as filed: the last 3 fiscal years, latest first.2
| Period ending | 2025-12-31 | 2024-12-31 | 2023-12-31 |
|---|---|---|---|
| Net loss | -$230.3M | -$121.2M | -$44.1M |
| Depreciation and amortization | $2.6M | $1.4M | $370.0K |
| Share-based compensation expense | $12.9M | $7.3M | $7.1M |
| Net periodic pension benefit (gain) loss for the qualified pension plan | -$58.0K | $1.0K | -$85.0K |
| Other non-cash items | -$1.0M | -$227.0K | $128.0K |
| Other receivables | -$2.0M | -$1.8M | -$840.0K |
| Operating lease right-of-use assets | $0 | -$6.0K | -$66.0K |
| Prepaid expenses | $561.0K | -$12.9M | -$6.3M |
| Other non-current assets | -$587.0K | $0 | $0 |
| Trade and other payables | $20.6M | $7.2M | $1.6M |
| Operating lease liabilities | -$1.2M | -$1.4M | -$222.0K |
| Accrued expenses and other current liabilities | $2.6M | $5.2M | -$327.0K |
| Net cash flow used in operating activities | -$196.0M | -$116.6M | -$42.8M |
| Purchase of short-term marketable debt securities | -$265.4M | -$350.3M | -$175.7M |
| Proceeds from maturities of short-term marketable debt securities | $468.4M | $145.2M | $150.8M |
| Purchase of property and equipment | -$35.0K | -$520.0K | -$284.0K |
| Net cash flow provided by (used in) investing activities | $203.0M | -$205.6M | -$25.2M |
| Proceeds from long-term debt, net of issuance costs | $73.0M | $0 | $0 |
| Issuance of Class A Ordinary Shares, net of transaction costs | $72.4M | $52.5M | $482.5M |
| Stamp duty on capital injection from MoonLake to MoonLake AG | $0 | -$1.5M | -$2.8M |
| Net cash flow provided by financing activities | $146.0M | $51.3M | $479.7M |
| Effect of movements in exchange rates on cash held | $1.1M | $128.0K | -$76.0K |
| Net change in cash and cash equivalents | $154.1M | -$270.7M | $411.7M |
| Cash paid for interest | $5.1M | $0 | $0 |
| Non-cash operating lease right-of-use assets obtained in exchange for lease obligations | $0 | $555.0K | $3.6M |
No quarter-by-quarter statement was filed.
Corporate structure
MoonLake Immunotherapeutics 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 MoonLake Immunotherapeutics
- Cormorant Asset Management, LP Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest Aug 14, 2026 (3 filings since Feb 17, 2026)
- Deep Track Capital, LP Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest Aug 14, 2026 (2 filings since Nov 12, 2025)
- T. Rowe Price Investment Management, Inc. Filed SCHEDULE 13G on MoonLake Immunotherapeutics, latest Aug 14, 2026
- BIOTECHNOLOGY VALUE FUND L P Filed SCHEDULE 13D/A on MoonLake Immunotherapeutics, latest Jun 29, 2026 (7 filings since Apr 18, 2022)
- Avoro Capital Advisors LLC Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest Nov 14, 2025 (2 filings since Aug 14, 2025)
- FMR LLC Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest Nov 5, 2025 (7 filings since Dec 10, 2021)
- Bihua Chen Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest Oct 1, 2025 (3 filings since Mar 31, 2023)
- PRICE T ROWE ASSOCIATES INC /MD/ Filed SCHEDULE 13G/A on MoonLake Immunotherapeutics, latest May 14, 2025 (4 filings since Feb 14, 2022)
- Healthcare Kgaa Merck Filed SC 13G/A on MoonLake Immunotherapeutics, latest Feb 15, 2024 (3 filings since Aug 3, 2022)
- CITADEL ADVISORS LLC Filed SC 13G/A on MoonLake Immunotherapeutics, latest Feb 14, 2024 (3 filings since Feb 14, 2022)
- ADAGE CAPITAL PARTNERS GP, L.L.C. Filed SC 13G/A on MoonLake Immunotherapeutics, latest Feb 9, 2023
- BlackRock Filed SC 13G/A on MoonLake Immunotherapeutics, latest Feb 3, 2022
- MoonLake Immunotherapeutics E9
Built from major holders from Schedules 13D and 13G. Each entity in the chart links to its source.
What it owns
What MoonLake Immunotherapeutics 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
| Item | Latest | A year before | Change |
|---|---|---|---|
| Property and equipment, net | $577.0K2 Dec 31, 2025 | $722.0K2 Dec 31, 2024 | −20.1% |
| Operating-lease assets (leased space) | $1.6M2 Dec 31, 2025 | $2.9M2 Dec 31, 2024 | −46.4% |
Investments
| Item | Latest | A year before | Change |
|---|---|---|---|
| Cash and cash equivalents | $334.5M2 Dec 31, 2025 | $180.4M2 Dec 31, 2024 | +85.4% |
| Marketable securities, current | $59.5M2 Dec 31, 2025 | $267.6M2 Dec 31, 2024 | −77.8% |
| Debt securities available for sale | $59.5M2 Dec 31, 2025 | $327.3M2 Dec 31, 2024 | −81.8% |
Properties, in its own words
Our corporate headquarters are located in Zug, Switzerland, where we occupy approximately 4,000 square feet of office space under two open-ended office lease agreements. We use this facility for administrative purposes. In addition, we have facilities in Cambridge, UK, where we occupy approximately 6,000 square feet of office space under a 3-year term agreement set to expire in October 2026. This facility serves as working space primarily for our research and development teams. Lastly, we have facilities in Porto, Portugal, where we occupy approximately 3,900 square feet of office space under a 3-year initial term agreement set to expire in October 2026, with two extendable periods of 3 years each, the first of which we expect to exercise through October 2029, and approximately 2,000 square feet of office space under a 2-year initial term agreement set to expire in October 2026, with two extendable periods of 3 years each, the first of which we expect to exercise through October 2029. These facilities serve as working space for our general and administrative teams. We believe that our facilities are sufficient to meet our current needs. We also believe we will be able to obtain additional space, as needed, on commercially reasonable terms.
Item 2 of the 10-K filed Feb 25, 2026.4
Leadership
Who has led MoonLake Immunotherapeutics, and when. Pick a name to see everywhere that person has worked.
Chief executive
Chair
Chief financial officer
- Chief executive officerDa Silva Jorge Santos Apr 15, 2022 to now12
- Chief executive officerBihua Chen Oct 19, 2020 to Oct 22, 202013
- ChairBihua Chen Oct 19, 2020 to Oct 22, 202013
- Chief financial officerMatthias Bodenstedt Apr 15, 2022 to now14
- Chief financial officerJay Scollins Oct 19, 2020 to Oct 19, 202015
Board members and other officers (10)
- Chief Scientific OfficerKristian Reich Apr 15, 2022 to now16
- Board memberAndrew John Phillips Apr 15, 2022 to now17
- Board memberCatherine Moukheibir Apr 15, 2022 to now18
- Board memberDa Silva Jorge Santos Apr 15, 2022 to now12
- Board memberKara Lassen Apr 15, 2022 to Apr 15, 202219
- Board memberMark N. Lampert Apr 15, 2022 to now20
- Board memberRamnik Xavier Apr 15, 2022 to now21
- Board memberSpike Loy Apr 15, 2022 to now22
- Board memberJohn P. Schmid Oct 19, 2020 to Oct 19, 202023
- Board memberNancy T. Chang Oct 19, 2020 to Oct 19, 202024
Former names
- Helix Acquisition CorpAug 28, 2020 to Mar 31, 20223
Timeline
- Sep 30, 20268-K Other events25
- Aug 10, 20268-K Results of operations; Regulation FD disclosure26
- Jul 15, 20268-K Other events27
- Jun 25, 20268-K Entered a material agreement28
- Jun 22, 20268-K Regulation FD disclosure; Other events29
- Jun 9, 20268-K Executive or director change; Shareholder vote30
- Jun 1, 20268-K Entered a material agreement31
- May 11, 20268-K Results of operations; Regulation FD disclosure32
- Feb 23, 20268-K Entered a material agreement; Results of operations; New debt or obligation33
- Jan 8, 20268-K Other events34
- Nov 5, 20258-K Results of operations; Regulation FD disclosure35
- Nov 5, 20258-K Entered a material agreement36
- Apr 15, 2022New chief executive Da Silva Jorge Santos becomes CEO12
- Oct 19, 2020New chief executive Bihua Chen becomes CEO13
Calendar
Coming up
- Nov 4, 2026Reports results for the quarter ending Sep/2026 A year earlier it reported ($1.10) a share, on Nov 5, 2025.37
When it reported results
- Aug 10, 2026Reported quarterly or annual results26
- May 11, 2026Reported quarterly or annual results32
- Feb 23, 2026Reported quarterly or annual results33
- Nov 5, 2025Reported quarterly or annual results35
- Aug 5, 2025Reported quarterly or annual results38
- May 12, 2025Reported quarterly or annual results39
- Feb 26, 2025Reported quarterly or annual results40
- Nov 7, 2024Reported quarterly or annual results41
Drug trials and FDA: coming up
- Jan 4, 2027Phase 3 trial readout expected Phase 3 trial of Sonelokimab and Risankizumab in Arthritis, Psoriatic: primary completion expected Jan 4, 2027 (ClinicalTrials.gov NCT06641089).42
Drug trials and FDA: recently
- May 28, 2026Phase 3 trial completed Phase 3 trial of Sonelokimab in Arthritis, Psoriatic: primary completion May 28, 2026, no results posted yet (ClinicalTrials.gov NCT06641076).43
- Sep 5, 2023Phase 2 trial completed Phase 2 trial of Sonelokimab and Adalimumab in Arthritis, Psoriatic: primary completion Sep 5, 2023, results posted Sep 10, 2026 (ClinicalTrials.gov NCT05640245).44
- May 9, 2023Phase 2 trial completed Phase 2 trial of Sonelokimab (M1095) and Adalimumab in Hidradenitis Suppurativa: primary completion May 9, 2023, results posted Sep 9, 2026 (ClinicalTrials.gov NCT05322473).45
Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). Trials from ClinicalTrials.gov, as the sponsor registered them (expected dates are the sponsor's own and often move); approvals and advisory committee meetings from the FDA. The FDA does not publish its decision (PDUFA) dates. The full markets calendar
Filings
293 filings to the SEC since October 2021: 7 annual reports, 16 quarterly reports, 51 major events, 89 insider forms, 38 large holders, 92 other. The latest 20:
- Sep 30, 20268-K CURRENT REPORT EDGAR
- Aug 14, 2026SCHEDULE 13G EDGAR
- Aug 14, 2026SCHEDULE 13G/A EDGAR
- Aug 14, 2026SCHEDULE 13G/A EDGAR
- Aug 10, 202610-Q EDGAR
- Aug 10, 2026S-8 REGISTRATION STATEMENT EDGAR
- Aug 10, 2026S-3ASR REGISTRATION STATEMENT EDGAR
- Aug 10, 20268-K CURRENT REPORT EDGAR
- Jul 29, 20264 EDGAR
- Jul 23, 20264 EDGAR
- Jul 21, 20264 EDGAR
- Jul 20, 20264 EDGAR
- Jul 15, 2026144 EDGAR
- Jul 15, 20268-K CURRENT REPORT EDGAR
- Jul 13, 20264 EDGAR
- Jul 2, 20264 EDGAR
- Jun 30, 2026144 EDGAR
- Jun 29, 2026SCHEDULE 13D/A EDGAR
- Jun 25, 20268-K CURRENT REPORT EDGAR
- Jun 24, 2026424B5 PROSPECTUS SUPPLEMENT EDGAR
The 293 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
56 open-market trades by officers, directors and large owners since October 2021: 10 buys and 46 sales. Grants, option exercises and gifts are left out.
| Date | Who | Trade | Shares | Price | Value | Filing |
|---|---|---|---|---|---|---|
| Jul 27, 2026 | Reich KristianChief Scientific Officer | Sale | 1,100 | $20.00 | $22.0K | Form 4 |
| Jul 22, 2026 | Reich KristianChief Scientific Officer | Sale | 2,448 | $20.00 | $49.0K | Form 4 |
| Jul 21, 2026 | Reich KristianChief Scientific Officer | Sale | 50,000 | $20.02 | $1.0M | Form 4 |
| Jul 20, 2026 | Reich KristianChief Scientific Officer | Sale | 43,700 | $20.09 | $877.9K | Form 4 |
| Jul 15, 2026 | Reich KristianChief Scientific Officer | Sale | 16,105 | $20.01 | $322.3K | Form 4 |
| Jul 10, 2026 | Santos da Silva JorgeChief Executive Officer | Sale | 68,289 | $20.02 | $1.4M | Form 4 |
| Jul 9, 2026 | Santos da Silva JorgeChief Executive Officer | Sale | 33,936 | $20.01 | $679.1K | Form 4 |
| Jul 1, 2026 | Santos da Silva JorgeChief Executive Officer | Sale | 47,775 | $20.03 | $956.9K | Form 4 |
| Jun 22, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 39,120 | $22.04 | $862.2K | Form 4 |
| Jun 18, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 2,794 | $19.60 | $54.8K | Form 4 |
| Jun 17, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 15,082 | $19.68 | $296.8K | Form 4 |
| Jun 17, 2026 | Reich KristianChief Scientific Officer | Sale | 50,000 | $19.43 | $971.5K | Form 4 |
| Jun 16, 2026 | Reich KristianChief Scientific Officer | Sale | 50,000 | $18.70 | $935.0K | Form 4 |
| Jun 15, 2026 | Reich KristianChief Scientific Officer | Sale | 50,000 | $18.89 | $944.5K | Form 4 |
| May 11, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 13,653 | $20.02 | $273.3K | Form 4 |
| Apr 14, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 2,426 | $19.56 | $47.5K | Form 4 |
| Apr 13, 2026 | Santos da Silva JorgeChief Executive Officer | Sale | 51,873 | $18.23 | $945.6K | Form 4 |
| Apr 10, 2026 | Santos da Silva JorgeChief Executive Officer | Sale | 98,127 | $18.41 | $1.8M | Form 4 |
| Apr 10, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 1,925 | $19.51 | $37.6K | Form 4 |
| Apr 9, 2026 | Bodenstedt MatthiasChief Financial Officer | Sale | 85,870 | $18.94 | $1.6M | Form 4 |
All 56 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.
- Cormorant Asset Management, LPSCHEDULE 13G/A, 3 filings Feb 17, 2026 to Aug 14, 202646
- Deep Track Capital, LPSCHEDULE 13G/A, 2 filings Nov 12, 2025 to Aug 14, 202647
- T. Rowe Price Investment Management, Inc.SCHEDULE 13G, 1 filing Aug 14, 202648
- BIOTECHNOLOGY VALUE FUND L PSCHEDULE 13D/A, 7 filings Apr 18, 2022 to Jun 29, 202649
- Avoro Capital Advisors LLCSCHEDULE 13G/A, 2 filings Aug 14, 2025 to Nov 14, 202550
- FMR LLCSCHEDULE 13G/A, 7 filings Dec 10, 2021 to Nov 5, 202551
- Bihua ChenSCHEDULE 13G/A, 3 filings Mar 31, 2023 to Oct 1, 202552
- PRICE T ROWE ASSOCIATES INC /MD/SCHEDULE 13G/A, 4 filings Feb 14, 2022 to May 14, 202553
- Healthcare Kgaa MerckSC 13G/A, 3 filings Aug 3, 2022 to Feb 15, 202454
- CITADEL ADVISORS LLCSC 13G/A, 3 filings Feb 14, 2022 to Feb 14, 202455
- ADAGE CAPITAL PARTNERS GP, L.L.C.SC 13G/A, 1 filing Feb 9, 202356
- BlackRockSC 13G/A, 1 filing Feb 3, 202257
- RA CAPITAL MANAGEMENT, L.P.SC 13G/A, 1 filing Nov 15, 202158
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.
| Year | Executive | Age | Salary | Total pay |
|---|---|---|---|---|
| 2025 | Dr. Jorge Santos da SilvaChief Executive Officer and Interim Chair of the Board | 49 | $762.4K | $4.9M59 |
| 2025 | Dr. Kristian ReichChief Scientific Officer | 60 | $762.4K | $4.8M59 |
| 2025 | Matthias BodenstedtChief Financial Officer | 38 | $603.6K | $4.7M59 |
| 2024 | Dr. Jorge Santos da SilvaChief Executive Officer and Interim Chair of the Board | 49 | $698.2K | $1.4M59 |
| 2024 | Dr. Kristian ReichChief Scientific Officer | 60 | $698.2K | $1.3M59 |
| 2024 | Matthias BodenstedtChief Financial Officer | 38 | $552.8K | $1.0M59 |
| 2023 | Dr. Kristian ReichChief Scientific Officer | 60 | $586.3K | $1.2M59 |
| 2023 | Dr. Jorge Santos da SilvaChief Executive Officer and Interim Chair of the Board | 49 | $586.3K | $1.2M59 |
| 2023 | Matthias BodenstedtChief Financial Officer | 38 | $446.8K | $891.6K59 |
Held by these funds
The largest holders among investment managers' 13F reports for the quarter ending Jun 30, 2026, the top 25 of 100. Change is in shares since the quarter before.
| Fund | Shares | Value | Share of the fund | Change |
|---|---|---|---|---|
| Bvf Inc/il | 16,001,284 | $311.5M | 8.0% | No change |
| Deep Track Capital, LP | 6,999,025 | $136.3M | 2.0% | +590,162 |
| D. E. Shaw & Co., Inc. | 3,365,507 | $65.5M | 0.0% | +974,846 |
| Cormorant Asset Management, LP | 3,205,433 | $62.4M | 3.2% | −1,275,000 |
| Jupiter Topco LLC | 3,085,906 | $60.1M | 0.0% | New |
| Logos Global Management LP | 2,675,000 | $52.1M | 2.2% | +1,175,000 |
| Weiss Asset Management LP | 2,581,813 | $50.3M | 0.7% | +873,485 |
| Citadel Advisors LLC | 1,972,893 | $38.4M | 0.0% | +649,165 |
| Two Sigma Investments, LP | 1,715,349 | $33.4M | 0.0% | +593,037 |
| Mpm Bioimpact LLC | 1,606,967 | $31.3M | 1.9% | −204,115 |
| Jpmorgan Chase & Co | 1,386,422 | $27.6M | 0.0% | +297,908 |
| Vivo Capital, LLC | 1,400,000 | $27.3M | 2.5% | +400,000 |
| Point72 Asset Management, L.P. | 1,158,732 | $22.6M | 0.0% | −209,786 |
| BlackRock, Inc. | 1,094,791 | $21.3M | 0.0% | +72,940 |
| Balyasny Asset Management L.P. | 912,715 | $17.8M | 0.0% | −152,895 |
| Great Point Partners LLC | 855,813 | $16.7M | 3.9% | +355,813 |
| Jane Street Group, LLC | 853,386 | $16.6M | 0.0% | +399,761 |
| Candriam S.C.A. | 769,766 | $15.0M | 0.1% | −48,360 |
| Bank Of America Corp /de/ | 751,897 | $14.6M | 0.0% | +27,103 |
| Arrowstreet Capital, Limited Partnership | 750,777 | $14.6M | 0.0% | +680,637 |
| Trails Edge Capital Partners, LP | 750,000 | $14.6M | 2.3% | New |
| Renaissance Technologies LLC | 643,268 | $12.5M | 0.0% | +366,496 |
| Millennium Management LLC | 636,187 | $12.4M | 0.0% | +60,095 |
| Morgan Stanley | 563,602 | $11.0M | 0.0% | −50,880 |
| Marshall Wace, Llp | 550,351 | $10.7M | 0.0% | +439,020 |
13F reports cover disclosed long positions in U.S. stocks only.
SEC filer profile
How MoonLake Immunotherapeutics is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.
- Name on EDGARMoonLake Immunotherapeutics1
- CIK0001821586
- Employer ID (EIN)98-17119634
- Filer statusLarge accelerated filer not an emerging growth company; not a smaller reporting company; not a shell company4
- Incorporated inCayman Islands4
- Fiscal year endsDecember 311
- Industry code (SIC)2834 Pharmaceutical Preparations1
- SEC reviewing officeOffice of Life Sciences, Division of Corporation Finance1
- Business addressDorfstrasse 29, Zug, V8 63001
- Phone41 41 510 80221
- Shares outstanding85,106,685 as of Aug 1, 20269
- Public float$1.3B as of Jun 30, 20254
- AuditorBaker Tilly US, LLP, Santa Clara, California PCAOB ID 23; it also attests to the company’s internal control over financial reporting4
- On EDGAR sinceAug 28, 20201
- Filings329 in all: 4 (81), 8-K (53), 10-Q (18), 3 (16), SC 13G/A (15), CORRESP (14), UPLOAD (14), 144 (13)1
All 40 form types
DEFA14A (10), SC 13G (10), SCHEDULE 13G/A (9), S-1/A (7), 10-K (6), 424B5 (6), EFFECT (6), 424B3 (5), SCHEDULE 13G (5), ARS (4), DEF 14A (4), PRER14A (4), SC 13D/A (3), SCHEDULE 13D/A (3), 10-K/A (2), POS AM (2), S-1 (2), S-3 (2), S-8 (2), 10-Q/A (1), 424B4 (1), 425 (1), 8-A12B (1), 8-K/A (1), CERT (1), DEFM14A (1), DEFR14A (1), DRS (1), NT 10-Q (1), PREM14A (1), S-3ASR (1), SC 13D (1)
- Latest filingsAnnual report (10-K) Feb 25, 2026
Quarterly report (10-Q) Aug 10, 2026
Proxy statement (DEF 14A) Apr 21, 2026
Latest 8-K (8-K) Sep 30, 2026
Securities registered for trading
| Class | Symbol | Exchange |
|---|---|---|
| Class A ordinary share, par value $0.0001 per share | MLTX | Nasdaq |
From the cover page of the 10-K filed Feb 25, 2026 (Section 12(b) of the Exchange Act).4
Risk factors and legal proceedings
The risks MoonLake Immunotherapeutics names in Item 1A of its 10-K filed Feb 25, 2026: 68 risks under these headings, as written.4
- Risks Related to Our Limited Operating History, Business, Financial Condition, and Results of Operations
- We have a limited operating history and have no products approved for commercial sale.
- We have incurred losses since inception, and we expect to incur significant losses for the foreseeable future and may not be able to achieve or sustain profitability in the future. We have not generated any revenue from SLK and may never generate revenue or become profitable.
- If we are unable to raise capital when needed, or on acceptable terms, we may be forced to delay, reduce and/or eliminate one or more of our development programs or future commercialization efforts, which would have a negative impact on our business, prospects, operating results and financial condition.
- Our business relies on certain licensing rights from MHKDG and RCT that can be terminated in certain circumstances. If we breach those agreements, or if we are unable to satisfy our diligence obligations under which we license rights to SLK from MHKDG, we could lose the ability to develop and commercialize SLK.
- Due to the significant resources required for the development of SLK, we must prioritize the pursuit of treatments for certain indications. We may expend our limited resources to pursue a particular indication and fail to capitalize on indications that may be more profitable or for which there is a greater likelihood of success.
- We may be required to take write-downs or write-offs, restructuring and impairment or other charges that could have a significant negative effect on our financial condition, results of operations and stock price, which could cause you to lose some or all of your investment.
- The only principal assets of our Company are cash and our interest in MoonLake AG, and accordingly we will depend on distributions from MoonLake AG to pay taxes and expenses.
- If the market opportunities for our approved product candidates, if any, are smaller than we expect, it could materially and adversely affect our financial condition and results of operation.
- Even if SLK or other compounds we may develop are successful in clinical trials and receive regulatory approvals, we or our collaboration partners may not be able to successfully commercialize them.
- The Loan and Security Agreement contains certain covenants that could adversely affect our operations and, if an event of default were to occur, we could be forced to repay any outstanding indebtedness sooner than planned and possibly at a time when we do not have sufficient capital to meet this obligation.
- Risks Related to Product Development
The other 57 risks
- We have never successfully completed the regulatory approval process for any of our product candidates and we may be unable to do so for any product candidates we acquire or develop.
- We are substantially dependent on the success of SLK, and our ongoing and anticipated clinical trials of SLK may not be successful.
- We may find it difficult to enroll patients in our clinical trials. If we experience delays or difficulties in the enrollment of patients in clinical trials, our successful completion of clinical trials or receipt of marketing approvals could be delayed or prevented.
- The results of preclinical testing and early clinical trials may not be predictive of the success of our later clinical trials, and the results of our clinical trials may not satisfy the requirements of the FDA, EMA, or other comparable foreign regulatory authorities.
- Preclinical and clinical development involves a lengthy and expensive process with uncertain outcomes, and results of earlier studies and trials may not be predictive of future clinical trial results.
- Preliminary, interim data from our clinical trials that we announce or publish may change as more patient data become available and are subject to audit and verification procedures.
- We face substantial competition, which may result in others discovering, developing, licensing or commercializing products before or more successfully than we do.
- SLK may have a safety profile that could prevent regulatory approval, marketing approval or market acceptance, or limit its commercial potential.
- Geopolitical events and global economic conditions, such as public health crises, the conflicts between Russia and Ukraine and in the Middle East, could seriously and adversely affect our preclinical studies and ongoing and anticipated clinical trials, business, financial condition and results of operations.
- Risks Related to Regulatory Process and Other Legal Compliance Matters
- The regulatory approval processes of the FDA, EMA, and other comparable foreign regulatory authorities are complex, time-consuming and inherently unpredictable. If we are not able to obtain, or if there are delays in obtaining, required regulatory approvals for SLK, we may not be able to commercialize, or may be delayed in commercializing, SLK, and our ability to generate revenue will be materially impaired.
- We will be subject to extensive 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 SLK.
- Disruptions at the FDA, the SEC and other government agencies and regulatory authorities caused by funding shortages or global health concerns could hinder their ability to hire and retain key leadership and other personnel, prevent new products and services from being developed or commercialized in a timely manner or otherwise prevent those agencies from performing normal business functions on which the operation of our business may rely, which could negatively impact our business.
- Due to unfavorable pricing regulations and/or third-party coverage and reimbursement policies, we may not be able to offer SLK at competitive prices which would seriously harm our business.
- Failure to comply with the laws and regulations prohibiting the promotion of off-label uses can result in, among other things, adverse publicity, warning letters, corrective advertising and potential civil and criminal penalties.
- Our employees, independent contractors, consultants, commercial collaborators, principal investigators, CROs, suppliers and vendors may engage in misconduct or other improper activities, including noncompliance with regulatory standards and requirements.
- Our business operations and current and future arrangements with investigators, healthcare professionals, consultants, third-party payors, patient organizations and customers will be subject to applicable healthcare regulatory laws, which could expose us to penalties.
- The healthcare system is under significant financial pressure to reduce costs, which could reduce payment and reimbursement rates for drugs.
- Pharmaceutical and biological product marketing is subject to substantial regulation in the United States and EU, and any failure by us or our future commercial and collaborative partners to comply with applicable statutes or regulations can adversely affect our business.
- 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.
- We are subject to laws and regulations related to privacy, data protection, information security and consumer protection across different markets where we conduct our business. Our actual or perceived failure to comply with such obligations could harm our business.
- We are subject to certain U.S. and foreign anti-corruption, anti-money laundering, export control, sanctions, and other trade laws and regulations. We can face serious consequences for violations.
- The Cayman Islands Economic Substance Act may affect our operations.
- Current and future legislation may increase the difficulty and cost for us, and any collaborators, to obtain marketing approval of and commercialize our drug candidates and affect the prices we, or they, may obtain.
- We may be subject to adverse legislative or regulatory tax changes that could negatively impact our financial condition.
- Risks Related to Employee Matters, Managing Our Growth and Other Risks Related to Our Business
- We are dependent on our key personnel and anticipate hiring new key personnel. If we are not successful in attracting and retaining qualified personnel, we may not be able to successfully implement our business strategy.
- In order to successfully implement our plans and strategies, we will need to grow the size of our organization and we may experience difficulties in managing this growth.
- A cybersecurity incident or failure in our information technology and storage systems or those of third parties upon whom we rely could significantly disrupt the operation of our business and adversely impact our financial condition.
- Our internal computer systems, or those of any of our CROs, manufacturers, other contractors or consultants or potential future collaborators, may fail or suffer security or data privacy breaches or other unauthorized or improper access to, use of, or destruction of our proprietary or confidential data, employee data or personal data, which could result in additional costs, loss of revenue, significant liabilities, harm to our brand and material disruption of our operations.
- Risks Related to Reliance on Third Parties
- We currently rely, and plan to rely in the future, on third parties to conduct and support our preclinical studies and clinical trials. If these third parties do not properly and successfully carry out their contractual duties or meet expected deadlines, we may not be able to obtain regulatory approval of or commercialize SLK.
- We currently rely on third parties to produce and process SLK. Our business could be adversely affected if the third-party manufacturers fail to provide us with sufficient quantities of SLK or fail to do so at acceptable quality levels or prices.
- We may, in the future, form or seek collaborations or strategic alliances or enter into licensing arrangements, and we may not realize the benefits of such collaborations, alliances or licensing arrangements.
- Risks Related to Our Intellectual Property
- Our ability to protect our patents and other proprietary rights is uncertain, exposing us to the possible loss of competitive advantage.
- We enjoy only limited geographical protection with respect to certain patents and may not be able to protect our intellectual property rights throughout the world.
- Obtaining and maintaining our 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 if we fail to comply with these requirements.
- Issued patents covering one or more of our drug candidates could be found invalid or unenforceable.
- We may be subject to damages resulting from claims that we or our employees have wrongfully used or disclosed confidential information of our competitors or are in breach of non-competition or non-solicitation agreements with our competitors.
- Patent terms may be inadequate to protect our competitive position with respect to SLK for an adequate amount of time.
- If we do not obtain patent term extension in the United States under the Hatch-Waxman Act and in foreign countries under similar legislation, thereby potentially extending the term of our marketing exclusivity for SLK, our business may be materially harmed.
- Changes to patent laws in the United States and other jurisdictions could diminish the value of patents in general, thereby impairing our ability to protect SLK.
- We may not identify relevant third-party patents or may incorrectly interpret the relevance, scope or expiration of a third-party patent, which might adversely affect our ability to develop and market SLK.
- We may be subject to claims challenging the inventorship of our patents and other intellectual property.
- We may be subject to patent infringement claims or may need to file claims to protect our intellectual property, which could result in substantial costs and liability and prevent us from commercializing SLK.
- We license patent rights from third-party owners and thus our rights to develop and commercialize our technology and product candidates are subject, in part, to the terms and conditions of licenses granted to us by others.
- Our license from MHKDG may be subject to retained rights.
- We may not be able to effectively secure first-tier technologies when competing against other companies or investors.
- Numerous factors may limit any potential competitive advantage provided by our intellectual property rights.
- If approved, our product candidates that are regulated as biologics may face competition from biosimilars approved through an abbreviated regulatory pathway.
- Risks Related to Our Class A Ordinary Shares
- The price of our shares has been, and may continue to be volatile, and you could lose all or part of your investment.
- If our share price is volatile, we may be subject to securities litigation, which is expensive and could divert management attention.
- Sales of our Class A Ordinary Shares, or the perception that such sales may occur, may cause the market price of the Class A Ordinary Shares to decline significantly, even if our business is doing well.
- Our principal shareholders and management own a significant percentage of our stock and are able to exert significant influence over matters subject to shareholder approval.
- Anti-takeover provisions in our organizational documents could delay or prevent a change of control.
- Our indemnification obligations to our officers and directors may result in a significant cost to us and hurt the interests of our shareholders.
- Because we do not anticipate paying any cash dividends on our capital stock in the foreseeable future, capital appreciation, if any, will be your sole source of gain.
- Future issuances of debt securities and equity securities may adversely affect our Company, including the market price of our Class A Ordinary Shares and may be dilutive to existing shareholders.
- General Risk Factors
- We may become a foreign private issuer within the meaning of the rules under the Exchange Act, and as such we would be exempt from certain provisions applicable to U.S. domestic public companies.
Legal proceedings
From time to time, we may become involved in legal proceedings arising in the ordinary course of our business. Regardless of outcome, litigation can have an adverse impact on us due to defense and settlement costs, diversion of management resources, negative publicity, reputational harm and other factors, and there can be no assurances that favorable outcomes will be obtained.
On October 15, 2025, a lawsuit captioned Bridgewood v. MoonLake Immunotherapeutics, et al., Case No. 1:25-cv-8500 (the “Bridgewood Action”) was filed in the United States District Court for the Southern District of New York, naming the Company, its Chief Executive Officer, and its Chief Financial Officer as defendants. The Bridgewood Action was purportedly brought on behalf of a class of all investors who purchased or otherwise acquired the Company’s common stock between March 10, 2024, through September 29, 2025 (the “Class Period”). The complaint alleged claims under Sections 10(b) and 20(a) of the Securities Exchange Act of 1934, as amended (“Exchange Act”), based on allegedly false or misleading statements related to the clinical benefits and prospects of SLK. The lawsuit sought unspecified damages and other relief. On October 22, 2025, the plaintiff voluntarily dismissed without prejudice the Bridgewood Action.
On October 17, 2025, a second putative class action captioned Peters v. MoonLake Immunotherapeutics, et al., Case No. 1:25-cv-8612 (the “Peters Action” and, together with the Bridgewood Action, the “Class Actions”) was filed in the United States District Court for the Southern District of New York (the “Court”). The Peters Action names the same defendants, contains identical allegations of alleged violations of the Exchange Act, covers the same Class Period, and seeks the same relief as the Bridgewood Action. On January 6, 2026, the Court appointed lead plaintiff and lead counsel.
The opening of Item 3, Legal Proceedings.4
Sources
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- 13SEC EDGARBihua Chen, Chief executive officer
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- 17SEC EDGARAndrew John Phillips, Board member
- 18SEC EDGARCatherine Moukheibir, Board member
- 19SEC EDGARKara Lassen, Board member
- 20SEC EDGARMark N. Lampert, Board member
- 21SEC EDGARRamnik Xavier, Board member
- 22SEC EDGARSpike Loy, Board member
- 23SEC EDGARJohn P. Schmid, Board member
- 24SEC EDGARNancy T. Chang, Board member
- 25SEC EDGAROther events
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- 27SEC EDGAROther events
- 28SEC EDGAREntered a material agreement
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- 31SEC EDGAREntered a material agreement
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- 34SEC EDGAROther events
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- 36SEC EDGAREntered a material agreement
- 37NasdaqNasdaq calendar
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