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Nuvectis Pharma (NASDAQ: NVCT) widens 2025 loss but boosts cash to $31.6M

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8-K

Rhea-AI Filing Summary

Nuvectis Pharma, Inc. reported wider losses for 2025 as it advanced its lead oncology candidate NXP900 through early-stage clinical development. Cash and cash equivalents were $31.6 million as of December 31, 2025, up from $18.5 million a year earlier, mainly from a February 2025 public offering and use of its at-the-market facility.

The company’s net loss was $26.4 million for 2025 compared with $19.0 million in 2024, driven by higher research and development and general and administrative expenses, including $6.0 million of non-cash stock-based compensation and $2.4 million of one-time license milestone fees. Research and development expenses rose to $18.2 million, while general and administrative costs increased to $9.4 million.

Management highlighted progress in the NXP900 program, including an ongoing Phase 1b monotherapy study across selected tumor types and a combination study with osimertinib in EGFR-mutated NSCLC, with a lorlatinib combination in ALK-positive NSCLC pending initiation. The company believes its current cash can fund multiple NXP900 Phase 1b milestones and operations well into the second half of 2027.

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Insights

Nuvectis increased its cash runway while spending more to advance NXP900 into Phase 1b studies.

Nuvectis Pharma ended 2025 with cash and cash equivalents of $31.6 million, up from $18.5 million, primarily from a February 2025 public offering and at-the-market sales. Management states this balance is expected to fund operations and multiple NXP900 Phase 1b milestones well into the second half of 2027.

Higher investment in development led to a larger net loss. Net loss rose to $26.4 million from $19.0 million, with research and development expenses increasing to $18.2 million and general and administrative expenses to $9.4 million. These figures include $6.0 million of non-cash stock-based compensation and $2.4 million of one-time license milestone fees.

The NXP900 program is in a Phase 1b monotherapy study and a combination trial with osimertinib in EGFR-mutated NSCLC, with a lorlatinib combination in ALK-positive NSCLC pending commencement. Actual value creation will depend on safety and efficacy data from these studies, which the company indicates could generate multiple data readouts during 2026.

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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): February 11, 2026

 

Nuvectis Pharma, Inc.

(Exact Name of Registrant as Specified in Charter)

 

Delaware
(State or Other Jurisdiction
of Incorporation)
  001-41264
(Commission File Number)
  86-2405608
(IRS Employer Identification No.)

 

1 Bridge Plaza Suite 275

Fort Lee, NJ 07024

(Address of Principal Executive Offices)

 

(201) 614-3150

(Registrant’s telephone number, including area code)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Securities registered pursuant to Section 12(b) of the Exchange Act:

 

Title of Class Trading Symbol(s) Exchange Name
Common Stock NVCT Nasdaq Capital Market

 

¨ Written communications pursuant to Rule 425 under the Securities Act.
   
¨ Soliciting material pursuant to Rule 14a-12 under the Exchange Act.
   
¨ Pre-commencement communications pursuant to Rule 14d-2b under the Exchange Act.
   
¨ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act.

 

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 x

 

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 Operations and Financial Condition.

 

On February 11, 2026, Nuvectis Pharma, Inc. issued a press release to provide a corporate update and to announce its financial results for the fiscal year ended December 31, 2025. A copy of such press release is being furnished as Exhibit 99.1 to this report.

 

The information, including Exhibit 99.1, in this Form 8-K is being furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that Section. The information in this Form 8-K shall not be incorporated by reference into any filing under the Securities Act of 1933, as amended, except as shall otherwise be expressly set forth by specific reference in such filing.

 

Item 9.01. Financial Statements and Exhibits.

 

(d) Exhibits.

 

The following exhibit is furnished herewith:

 

Exhibit    
Number   Description
99.1   Press release issued by Nuvectis Pharma, Inc., dated February 11, 2026.
104   Cover Page Interactive Data File, formatted in Inline Extensible Business Reporting Language (iXBRL).

 

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  Nuvectis Pharma, Inc.
  (Registrant)
     
Date: February 11, 2026    
     
  By: /s/ Ron Bentsur
    Ron Bentsur
    Chairman, Chief Executive Officer and President

 

 

 

 

Exhibit 99.1

 

 

 

Nuvectis Pharma, Inc. Reports 2025 Financial Results and Business Highlights

 

Fort Lee, NJ, February 11, 2026 (GLOBE NEWSWIRE) - Nuvectis Pharma, Inc. (NASDAQ: NVCT) ("Nuvectis" or the "Company"), a clinical-stage biopharmaceutical company focused on the development of innovative precision medicines for the treatment of serious conditions of unmet medical need in oncology, today reported its financial results for the year ended December 31, 2025 and provided an update on recent business progress.

 

Ron Bentsur, Chairman and Chief Executive Officer of Nuvectis, commented, “2025 was an eventful year for Nuvectis, with significant progress made in the NXP900 development program, laying the groundwork for multiple potential data readouts in 2026. Our Phase 1b monotherapy study evaluating NXP900’s clinical potential in several molecularly and histologically-defined target tumors, and the combination study of NXP900 with osimertinib in patients with EGFR-mutated non-small cell lung cancer (“NSCLC”) are enrolling patients. In addition, a combination with lorlatinib in ALK-positive NSCLC, is pending commencement. With the potential embedded in the NXP900 Phase 1b program, we expect 2026 to be an exciting year for Nuvectis.”

 

Mr. Bentsur concluded, “We remain focused on operational execution and financial responsibility, and believe that our current cash position can take us through multiple potential NXP900 Phase 1b milestones and well into the second half of 2027.”

 

Full Year 2025 Financial Results

 

Cash and cash equivalents were $31.6 million as of December 31, 2025, compared to $18.5 million as of December 31, 2024. The increase of $13.1 million resulted from the Company's February 2025 public offering and from access to our at-the-market facility, partially offset by operating expenses.

 

The Company's net loss was $26.4 million for the year ended December 31, 2025, compared to $19.0 million for the year ended December 31, 2024, an increase in net loss of $7.4 million. Net loss for the 2025 fiscal year included $6.0 million in non-cash stock-based compensation and one-time license fees associated with milestone achievements of $2.4 million.

Research and development expenses, including non-cash and one-time non-recurring expenses, were $18.2 million for the year ended December 31, 2025, compared to $12.9 million for the year ended December 31, 2024, an increase of $5.3 million.

 

General and administrative expenses, including non-cash and one-time non-recurring expenses, were $9.4 million for the year ended December 31, 2025, compared to $6.9 million for the year ended December 31, 2024, an increase of $2.5 million.

 

Finance income was $1.1 million for the year ended December 31, 2025, compared to $0.8 million for the year ended December 31, 2024, an increase of $0.3 million.

 

 

 

 

 

 

About Nuvectis Pharma, Inc.

 

Nuvectis Pharma, Inc. is a biopharmaceutical company focused on the development of innovative precision medicines for the treatment of serious conditions of unmet medical need in oncology. The Company's assets include NXP900 a clinical-stage drug candidate. NXP900 is an oral small molecule inhibitor of the SRC Family of Kinases (SFK), including SRC and YES1. Its unique mechanism of action enables inhibition of both the catalytic and scaffolding functions of the SRC kinase, providing comprehensive shutdown of the signaling pathway. NXP900 has completed a Phase 1a dose escalation study and the Phase 1b program has been initiated.

 

For more information on Nuvectis, please visit our website at https://nuvectis.com/.

 

Forward Looking Statements

 

This press release contains "forward-looking statements" within the meaning of the U.S. federal securities laws, which are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as "anticipate", "believe", "contemplate", "could", "estimate", "expect", "intend", "seek", "may", "might", "plan", "potential", "predict", "project", "target", "aim", "should", "will", "would", or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward looking statements are based on Nuvectis Pharma, Inc.'s current expectations and interpretations of data and information available, including preclinical and clinical safety, pharmacokinetics, pharmacodynamics, and efficacy data generated to date for NXP900 and the timing and safety and efficacy data expectations for the monotherapy and combination components of the NXP900 Phase 1b program and estimates and projections regarding our financial condition. The outcomes of the events described in these forward-looking statements are subject to inherent uncertainties, risks, assumptions, market and other conditions, and other factors that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties may also be subject to market and other conditions and described more fully in the section titled "Risk Factors" in our 2025 Form 10-K and our other public filings with the U.S. Securities and Exchange Commission ("SEC"). However, these risks are not exhaustive and new risks and uncertainties emerge from time to time, and it is not possible for us to predict all risks and uncertainties that could have an impact on the forward looking statements contained in this press release or other filings with the SEC. Any forward-looking statements contained in this press release speak only as of the date of this press release. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as may be required by law, and we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.

 

 

 

 

 

 

 

 

 

Company Contact:

 

Ron Bentsur

Chairman, Chief Executive Officer and President

rbentsur@nuvectis.com

  

Media Relations Contact:

 

Kevin Gardner

LifeSci Advisors

kgardner@lifesciadvisors.com

 

 

 

 

 

 

 

NUVECTIS PHARMA, INC.

 

BALANCE SHEETS

 

(USD in thousands, except per share and share amounts)

 

   December 31, 
   2025   2024 
Assets          
CURRENT ASSETS          
Cash and cash equivalents  $31,634   $18,533 
Other current assets   75    74 
TOTAL CURRENT ASSETS   31,709    18,607 
           
TOTAL ASSETS  $31,709   $18,607 
           
Liabilities and Shareholders’ Equity          
           
CURRENT LIABILITIES          
Accounts payables  $6,274   $2,498 
Accrued liabilities   115    840 
Employee compensation and benefits   6,907    5,556 
TOTAL CURRENT LIABILITIES   13,296    8,894 
TOTAL LIABILITIES   13,296    8,894 
           
COMMITMENTS AND CONTINGENCIES, see Note 3          
           
SHAREHOLDERS’ EQUITY, see Note 6          
Common Shares, $0.00001 par value – 60,000,000 shares authorized as of December 31, 2025, and December 31, 2024, 25,676,798, and 19,495,683 shares issued and outstanding as of December 31, 2025 and December 31, 2024, respectively   *    * 
Additional paid in capital   118,100    82,958 
Accumulated deficit   (99,687)   (73,245)
TOTAL SHAREHOLDERS’ EQUITY   18,413    9,713 
TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY  $31,709   $18,607 

 

*Represent amount lower than $1,000 USD.

  

 

 

  

 

 

NUVECTIS PHARMA, INC.

 

STATEMENT OF OPERATIONS

 

(USD in thousands, except per share and share amounts)

 

   For the year ended   For the year ended 
   December 31, 2025   December 31, 2024 
OPERATING EXPENSES          
Research and development  $18,153   $12,918 
General and administrative   9,421    6,929 
           
OPERATING LOSS   (27,574)   (19,847)
Finance income   1,132    847 
           
NET LOSS  $(26,442)  $(19,000)
EFFECT OF WARRANTS MODIFICATION,   (2,429)    
TOTAL NET LOSS ATTRIBUTABLE TO COMMON SHAREHOLDERS   (28,871)   (19,000)
BASIC AND DILUTED NET LOSS PER COMMON SHARE OUTSTANDING  $(1.32)  $(1.11)
Basic and diluted weighted average number of common shares outstanding   21,812,716    17,113,169 
           

 

 

 

FAQ

How much cash did Nuvectis Pharma (NVCT) have at the end of 2025?

Nuvectis Pharma ended 2025 with $31.6 million in cash and cash equivalents. This increased from $18.5 million at December 31, 2024, primarily due to a February 2025 public offering and use of its at-the-market facility, partially offset by operating expenses during the year.

What was Nuvectis Pharma’s net loss for 2025 and how did it change from 2024?

Nuvectis Pharma reported a 2025 net loss of $26.4 million, up from $19.0 million in 2024. The $7.4 million increase reflects higher research and development and general and administrative expenses, including $6.0 million of non-cash stock-based compensation and $2.4 million in one-time license milestone fees.

How much did Nuvectis Pharma spend on research and development in 2025?

Research and development expenses were $18.2 million for 2025, versus $12.9 million in 2024. This increase of $5.3 million includes non-cash and one-time non-recurring expenses, reflecting expanded clinical activity around the company’s lead candidate NXP900 and broader development work.

What were Nuvectis Pharma’s general and administrative expenses in 2025?

General and administrative expenses totaled $9.4 million in 2025, compared with $6.9 million in 2024. The $2.5 million increase includes non-cash and non-recurring items and reflects higher corporate and supporting costs as the company advances its clinical pipeline and grows its operations.

What progress did Nuvectis Pharma report on its NXP900 clinical program?

Nuvectis highlighted significant 2025 progress in its NXP900 program. A Phase 1b monotherapy trial across selected tumor types and a combination study with osimertinib in EGFR-mutated NSCLC are enrolling patients, while a planned combination with lorlatinib in ALK-positive NSCLC is pending commencement, supporting multiple data readouts in 2026.

How long does Nuvectis Pharma expect its cash runway to last based on 2025 results?

Management believes its current cash can fund operations well into the second half of 2027. This runway is expected to cover multiple potential milestones from the NXP900 Phase 1b program, including monotherapy and combination studies, assuming expenses and development progress track current internal expectations.

How did Nuvectis Pharma’s shareholders’ equity change between 2024 and 2025?

Shareholders’ equity increased to $18.4 million at December 31, 2025, from $9.7 million a year earlier. The change mainly reflects capital raised, which lifted additional paid-in capital to $118.1 million, offset by a higher accumulated deficit of $99.7 million from ongoing net losses.

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