STOCK TITAN

Lexicon Pharmaceuticals (Nasdaq: LXRX) narrows 2025 loss and raises fresh capital

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Lexicon Pharmaceuticals reported 2025 results showing higher revenue and a sharply reduced loss while advancing its pipeline. Total revenues were $49.8 million in 2025 versus $31.1 million in 2024, largely driven by $45 million of licensing revenue from a Novo Nordisk agreement and $4.6 million of INPEFA net sales.

Net loss narrowed to $50.3 million, or $0.14 per share, from $200.4 million, or $0.63 per share, helped by major cost reductions. Research and development expenses fell to $61.1 million from $84.5 million, and selling, general and administrative expenses dropped to $37.3 million from $143.1 million, reflecting a strategic repositioning and reduced INPEFA marketing.

As of December 31, 2025, cash, investments and restricted cash totaled $125.2 million, and in February 2026 the company added approximately $96.7 million of net equity proceeds plus a $10 million milestone payment from Novo Nordisk. Key programs progressed, including SONATA-HCM Phase 3 enrollment surpassing 50%, planned 2026 NDA resubmission for ZYNQUISTA in type 1 diabetes, and Phase 3 readiness for pilavapadin in diabetic neuropathic pain.

Positive

  • Substantial loss reduction with disciplined spending: Net loss shrank to $50.3 million in 2025 from $200.4 million in 2024, aided by cutting SG&A to $37.3 million from $143.1 million and R&D to $61.1 million from $84.5 million while still advancing key trials.
  • Strengthened balance sheet and non-dilutive potential: Cash, investments and restricted cash were $125.2 million at December 31, 2025, followed by approximately $96.7 million of net equity proceeds and a $10 million Novo Nordisk milestone, plus eligibility for up to $1 billion in future milestones and tiered royalties on LX9851.

Negative

  • Ongoing losses and lower product sales baseline: Despite improvements, Lexicon still recorded a 2025 net loss of $50.3 million and reported lower INPEFA net product revenue of $4.6 million versus $6.0 million in 2024, reflecting reduced marketing after its strategic repositioning.

Insights

Lexicon sharply narrows losses, bolsters cash, and advances several late-stage cardiometabolic and pain programs.

Lexicon grew 2025 revenue to $49.8 million from $31.1 million, mainly from a Novo Nordisk licensing deal. More importantly, it cut its net loss to $50.3 million from $200.4 million as R&D and SG&A spending fell substantially after a 2024 strategic repositioning.

Cost discipline reduced SG&A to $37.3 million from $143.1 million and R&D to $61.1 million from $84.5 million, while still funding pivotal SONATA-HCM and preparations for pilavapadin Phase 3. This combination of lower burn and continued clinical progress can make the pathway to potential future approvals more financially sustainable.

Liquidity is a key improvement: year-end cash, investments and restricted cash were $125.2 million, followed in February 2026 by about $96.7 million of net equity proceeds and a $10 million Novo Nordisk milestone. The Novo agreement also carries up to $1 billion in potential future milestones and tiered royalties, though realization depends on successful development and commercialization outcomes.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
0001062822FALSE00010628222026-03-052026-03-05


UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
__________________

FORM 8-K
__________________

CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): March 5, 2026

Lexicon Pharmaceuticals, Inc.
(Exact name of registrant as specified in its charter)
Delaware000-3011176-0474169
(State or other jurisdiction of
incorporation or organization)
(Commission File Number)(I.R.S. Employer
Identification Number)

2445 Technology Forest Blvd., 11th Floor
The Woodlands, Texas 77381
(Address of principal executive offices and Zip Code)

(281) 863-3000
(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading Symbol(s)Name of each exchange on which registered
Common Stock, par value $0.001LXRX
The Nasdaq Global Select Market
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligations of the registrant under any of the following provisions:
    Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
    Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
    Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
    Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.





Item 2.02     Results of Operation and Financial Condition

On March 5, 2026, we issued a press release to report our financial results for the quarter and year ended December 31, 2025. A copy of the press release is attached to this current report on Form 8-K as Exhibit 99.1.

The information in this Form 8-K and the Exhibit attached to this Form 8-K shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific reference in such a filing.


Item 9.01    Financial Statements and Exhibits

(d)    Exhibits

Exhibit No.Description
99.1
Press Release of Lexicon Pharmaceuticals, Inc. dated March 5, 2026
EX-104Cover Page Interactive Data File (embedded within the Inline XBRL document)




Signatures

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
Lexicon Pharmaceuticals, Inc.
Date: March 5, 2026By:/s/ Brian T. Crum
Brian T. Crum
Senior Vice President and General Counsel





Exhibit 99.1

LEXICON PHARMACEUTICALS REPORTS FOURTH QUARTER 2025
FINANCIAL RESULTS AND PROVIDES CLINICAL UPDATES


Pivotal sotagliflozin milestones on schedule including resubmission of NDA in T1D and enrollment of SONATA study for HCM

Positive End-of-Phase 2 meeting with FDA for pilavapadin confirms Phase 3 readiness and supports ongoing partnership discussions

Strengthened financial position with more than $100 million in additional cash from capital raise and Novo Nordisk milestone payment

Conference call and webcast at 8:30 am ET

The Woodlands, Texas, March 5, 2026Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX), today reported financial results for the three months and year ended December 31, 2025, and provided an update on key corporate milestones and accomplishments.

“The fourth quarter of 2025 marked the completion of an incredible year for Lexicon,” said Mike Exton, Ph.D., Lexicon’s chief executive officer and director. “We made substantial progress on all aspects of the business by advancing our pipeline programs, establishing strong development and commercialization agreements with leading global collaborators, working closely with regulators, and remaining operationally efficient. As a result, we have begun 2026 with tremendous momentum and are well-positioned to successfully execute on multiple important catalysts ahead.”

Scott Coiante, Lexicon’s senior vice president and chief financial officer, further commented, “Over the past year, we have pulled multiple levers to strengthen our financial position and extend our cash runway to support our robust clinical development pipeline. Our recent capital raise and milestone payment received from Novo Nordisk resulted in more than $100 million in additional cash in February 2026, which together with our rigorous expense discipline in 2025, provides the financial footing needed to support our pipeline programs.”

Fourth Quarter 2025 Business and Pipeline Highlights

Cardiometabolic

Sotagliflozin
Sotagliflozin is an oral inhibitor of sodium-glucose cotransporter types 1 and 2 (SGLT1 and SGLT2) and has been studied in approximately 20,000 patients across multiple cardiometabolic indications. Sotagliflozin is commercially available in the U.S. for heart failure as INPEFA®.

Hypertrophic Cardiomyopathy (HCM)
Enrollment continues in SONATA-HCM, a pivotal Phase 3 placebo-controlled study with a targeted enrollment of 500 patients with obstructive or nonobstructive HCM.
Lexicon has completed the initiation of 130 sites in 20 countries across the United States, Europe and Latin America.
The study has surpassed 50 percent enrollment and Lexicon continues to expect enrollment completion in mid-2026, with topline results in the first quarter of 2027.




Type 1 Diabetes (T1D) (ZYNQUISTA®)
Lexicon remains focused on bringing ZYNQUISTA to market for glycemic control in adults with T1D, a patient population which has not benefitted from a new treatment mechanism since the discovery of insulin.
Based on U.S. Food and Drug Administration (FDA) feedback, Lexicon remains on track for potential New Drug Application (NDA) resubmission and regulatory approval in 2026 if the patient exposure and safety data requirements identified by the FDA are achieved by STENO1, a third-party funded, investigator-initiated study of sotagliflozin being conducted by the STENO Diabetes Center (Denmark).

Viatris License for All Indications Ex-U.S. and Ex-Europe
Lexicon continues to support licensee Viatris in its regulatory filing and commercial strategy for sotagliflozin outside of the U.S. and Europe and in 2025 shipped the first commercial product to the United Arab Emirates, the first country to obtain approval outside of the U.S.
Viatris submitted applications for regulatory approval in several other markets in 2025, including Canada, Australia and New Zealand, and preparations are underway by Viatris for regulatory submissions in additional ex-U.S. and ex-European markets throughout 2026.

LX9851 for Obesity and Associated Cardiometabolic Disorders
LX9851 is a first-in-class, non-incretin, oral, small molecule inhibitor of acyl-CoA synthetase 5 (ACSL5) in development by Novo Nordisk for obesity and weight management.

All Investigational New Drug (IND) application-enabling activities were completed by Lexicon in 2025.
In February 2026, the company received a $10 million milestone payment from Novo Nordisk, with potential for up to $20 million in additional milestone payments in 2026.
Under the terms of Lexicon’s exclusive license agreement with Novo Nordisk, Lexicon received an upfront payment of $45 million in April 2025 and is eligible to receive up to an aggregate of $1 billion in upfront and development, regulatory and sales milestone payments. Lexicon is also eligible for tiered royalties on net sales of LX9851.

Pain

Pilavapadin (LX9211) for Diabetic Peripheral Neuropathic Pain (DPNP)
Pilavapadin is an orally delivered, small molecule drug candidate for the treatment of DPNP, among other potential indications. Pilavapadin has the potential to be the first oral, non-opioid drug therapy approved in neuropathic pain in more than 20 years.

Lexicon and the FDA held a successful End-of-Phase 2 meeting in the fourth quarter of 2025. The FDA raised no objections to the advancement of pilavapadin into Phase 3 development, which would include two placebo-controlled, 12-week, two arm registrational studies comparing the 10 mg daily dose to placebo. The primary endpoint of the Phase 3 studies would be the change in average daily pain score (ADPS) from baseline to Week 12.
Lexicon continues to hold partnership discussions to maximize the global potential of this investigative therapy.

Fourth Quarter 2025 Financial Highlights

Revenues: Total revenues were $5.5 million and $49.8 million for the quarter and year ended December 31, 2025, respectively. Revenues for the fourth quarter of 2025 include $4.3 million of licensing revenue from the Novo Nordisk agreement and net sales of INPEFA of $1.1 million.



Revenues for the year ended December 31, 2025, include $45 million of licensing revenue from the Novo Nordisk agreement and $4.6 million of net sales of INPEFA.

Total revenues for the fourth quarter and full year 2024 include the upfront payment of $25 million received upon entering into the Viatris license agreement and net sales of INPEFA of $1.6 million and $6.0 million, respectively.

Research and Development (R&D) Expenses: Research and development expenses for the fourth quarter of 2025 decreased to $11.3 million from $26.7 million in 2024. Full-year 2025 research and development expenses decreased to $61.1 million from $84.5 million in 2024, primarily reflecting lower external research expense on our PROGRESS clinical trial partially offset by increased investment in the SONATA Phase 3 clinical trial.

Selling, General and Administrative (SG&A) Expenses: Selling, general and administrative expenses for the fourth quarter of 2025 decreased to $8.8 million from $32.3 million in 2024. Full-year 2025 selling, general and administrative expenses decreased to $37.3 million from $143.1 million in 2024. The decrease in 2025 reflects lower costs resulting from the Company’s strategic repositioning in late 2024 and the significantly reduced marketing and promotional efforts for INPEFA in 2025.

Net Loss: Net loss for the fourth quarter of 2025 was $15.5 million, or $0.04 per share, compared to a net loss of $33.8 million, or $0.09 per share, in the corresponding period in 2024. Net loss for the full year 2025 was $50.3 million, or $0.14 per share, compared to a net loss of $200.4 million, or $0.63 per share, in the corresponding period in 2024. For the fourth quarters of 2025 and 2024, net loss included non-cash, stock-based compensation expense of $2.8 million and $1.5 million, respectively and for the full years of 2025 and 2024, net loss included non-cash, stock-based compensation expense of $12.5 million and $13.5 million, respectively.

Cash, Investments, and Restricted Cash: As of December 31, 2025, Lexicon had $125.2 million in cash, investments and restricted cash, as compared to $238.0 million in cash and investments as of December 31,2024.

In February 2026, Lexicon received approximately $96.7 million of net proceeds from the sale of common and preferred stock and also received a $10 million milestone payment from Novo Nordisk.

Conference Call and Webcast Information
Lexicon management will hold a live conference call and webcast today at 8:30 am ET / 7:30 am CT to review its financial and operating results and to provide a general business update. A live audio webcast of the call can be accessed by visiting the Events page of the Company’s investor relations website at https://investors.lexpharma.com/. Participants who wish to ask a question may register here to receive dial-in numbers and a unique pin to join the call. An archived version of the webcast will be available on the website for 30 days.

About Lexicon Pharmaceuticals
Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients’ lives. Lexicon has a pipeline of drug candidates in discovery, preclinical, and clinical development in neuropathic pain, hypertrophic cardiomyopathy (HCM), obesity and metabolic disorders, and other cardiometabolic indications. For additional information, please visit www.lexpharma.com.

Safe Harbor Statement
This press release contains “forward-looking statements,” including statements relating to Lexicon’s financial position and long-term outlook on its business, including the commercialization of its



approved products and the clinical development of regulatory filings for, and potential therapeutic and commercial potential of its other drug candidates. In addition, this press release also contains forward looking statements relating to Lexicon’s growth and future operating results, discovery, development and commercialization of products, strategic alliances and intellectual property, as well as other matters that are not historical facts or information. All forward-looking statements are based on management’s current assumptions and expectations and involve risks, uncertainties and other important factors, specifically including Lexicon’s ability to meet its capital requirements, successfully commercialize its approved products, successfully conduct preclinical and clinical development and obtain necessary regulatory approvals of its other drug candidates on its anticipated timelines, achieve its operational objectives, obtain patent protection for its discoveries and establish strategic alliances, as well as additional factors relating to manufacturing, intellectual property rights, and the therapeutic or commercial value of its approved products and other drug candidates. Any of these risks, uncertainties and other factors may cause Lexicon’s actual results to be materially different from any future results expressed or implied by such forward-looking statements. Information identifying such important factors is contained under “Risk Factors” in Lexicon’s annual report on Form 10-K for the year ended December 31, 2024, as filed with the Securities and Exchange Commission. Lexicon undertakes no obligation to update or revise any such forward-looking statements, whether as a result of new information, future events or otherwise.















Lexicon Pharmaceuticals, Inc.
Selected Financial Data
Consolidated Statements of Operations DataThree Months Ended December 31,Years Ended December 31,
(In thousands, except per share data)2025202420252024
(Unaudited)(Unaudited)
Revenues:
   Net product revenue$1,055 $1,550 $4,647 $6,001
   Licensing revenue4,30225,00045,00025,000
   Royalties and other revenue136415680
Total revenues5,49326,55449,80331,081
Operating expenses:
   Cost of sales201348274616
   Research and development, including stock-based
      compensation of $1,263, $1,106, $6,289 and $5,839, respectively11,31526,68561,12184,480
   Selling, general and administrative, including stock-based
      compensation of $1,572, $431, $6,228, and $7,660, respectively8,75732,25837,319143,102
Total operating expenses20,27359,29198,714228,198
Loss from operations(14,780)(32,737)(48,911)(197,117)
Interest and other expense(2,031)(3,858)(8,339)(15,579)
Interest income and other, net1,2812,8296,90912,293
Net loss$(15,530)$(33,766)$(50,341)$(200,403)
Net loss per common share, basic and diluted$(0.04)$(0.09)$(0.14)$(0.63)
Weighted average common shares outstanding,
   basic and diluted363,428361,492363,053320,031
As ofAs of
Consolidated Balance Sheet DataDecember 31, 2025December 31, 2024
(In thousands)
Cash and investments$96,230 $237,957
Restricted cash29,000
Property and equipment, net1,8632,484
Goodwill44,54344,543
Total assets184,987298,420
Current portion of long-term debt4,595
Long-term debt, net49,408100,298
Accumulated deficit(2,017,583)(1,967,242)
Total stockholders' equity107,538145,950




For Investor and Media Inquiries:
Lisa DeFrancesco
Lexicon Pharmaceuticals, Inc.
lexinvest@lexpharma.com


FAQ

How did Lexicon Pharmaceuticals (LXRX) perform financially in 2025?

Lexicon’s 2025 total revenues were $49.8 million, up from $31.1 million in 2024, driven mainly by $45 million of Novo Nordisk licensing revenue. Net loss narrowed significantly to $50.3 million, or $0.14 per share, from $200.4 million, or $0.63 per share.

What is the cash position of Lexicon Pharmaceuticals (LXRX) after recent financing?

At December 31, 2025, Lexicon held $125.2 million in cash, investments and restricted cash. In February 2026, it received approximately $96.7 million of net proceeds from common and preferred stock sales plus a $10 million milestone payment from Novo Nordisk, further strengthening liquidity.

What progress did Lexicon report on its SONATA-HCM study for sotagliflozin?

Lexicon’s SONATA-HCM Phase 3 trial surpassed 50% enrollment, targeting 500 patients with obstructive or nonobstructive hypertrophic cardiomyopathy. The company has initiated 130 sites in 20 countries and continues to expect enrollment completion in mid-2026 with topline results in the first quarter of 2027.

What are the regulatory plans for ZYNQUISTA (sotagliflozin) in type 1 diabetes?

Lexicon remains focused on bringing ZYNQUISTA to adults with type 1 diabetes. Based on FDA feedback, it is on track for a potential 2026 NDA resubmission and regulatory approval, if patient exposure and safety data requirements are met through the STENO1 investigator-initiated study.

What is the scope of Lexicon’s Novo Nordisk collaboration for LX9851?

Under an exclusive license, Lexicon received a $45 million upfront payment in April 2025 and a $10 million milestone in February 2026 for LX9851. The company is eligible for up to $1 billion in additional milestones plus tiered royalties on future LX9851 net sales.

What is the status of pilavapadin (LX9211) for diabetic peripheral neuropathic pain?

Lexicon held a successful End-of-Phase 2 meeting with the FDA in the fourth quarter of 2025. The agency raised no objections to advancing pilavapadin into Phase 3, with two planned 12-week registrational studies comparing a 10 mg daily dose to placebo using average daily pain score as the primary endpoint.

Filing Exhibits & Attachments

4 documents