STOCK TITAN

NuCana Reports Fourth Quarter and Year-End 2025 Financial Results and Provides Business Update

(Neutral)
Tags

NuCana (NASDAQ: NCNA) reported Q4 and full-year 2025 results and a clinical update on its ProTide pipeline. NUC-7738 showed clinical activity in PD-1 inhibitor-resistant melanoma with partial responses; final Phase 2 expansion data expected in 2026. Cash and equivalents were £24.3M at year‑end, supporting operations into 2029. The company reported a 2025 net loss of £29.4M, reflecting non-cash warrant revaluations and elevated share-based payments.

Key near-term priorities include completing NuTide:701 enrollment, seeking FDA guidance on a registrational path, and advancing NUC-3373 combinations.

Loading...
Loading translation...

Positive

  • Cash runway into 2029 with £24.3M cash at Dec 31, 2025
  • Phase 2 NUC-7738 showed clinical activity, including two partial responses
  • Raised gross proceeds of £28.6M from 2025 financings

Negative

  • Net loss increased to £29.4M in 2025 from £19.0M in 2024
  • Non-cash finance expense of £12.6M from warrant revaluation
  • Share-based payment expense rose to £10.0M in 2025

News Market Reaction – NCNA

-3.51%
5 alerts
-3.51% Session close to close
-10.2% Trough in 9 hr 19 min
$12.26M Market Cap
0.4x Rel. Volume

In the Mar 20 session, NCNA declined 3.51%, reflecting a moderate negative market reaction. Argus tracked a trough of -10.2% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement combines year-end 2025 results with updates on NUC‑7738 and NUC‑3373, highlighting...
Analysis

This announcement combines year-end 2025 results with updates on NUC‑7738 and NUC‑3373, highlighting clinical activity in PD‑1 inhibitor‑resistant melanoma and a cash runway expected to extend into 2029. Investors may focus on the strengthened cash balance of £24.3m, offset by a higher £29.4m annual net loss driven by warrant and share-based expenses. Upcoming 2026 NUC‑7738 data, FDA guidance, and funding discipline remain key watchpoints.

Key Figures

Cash & equivalents: £24.3 million May 2025 financing: £9.6 million ATM proceeds: £19.0 million +5 more
8 metrics
Cash & equivalents £24.3 million As at December 31, 2025 (vs £6.7 million at December 31, 2024)
May 2025 financing £9.6 million Gross proceeds (including £5.2m upfront and £4.4m from warrants)
ATM proceeds £19.0 million Gross proceeds raised in July 2025 via at-the-market program
Warrant cancellation cost $3.6 million Payments to cancel remaining Series A Warrants from May 2025 financing
Q4 2025 net loss £2.5 million Quarter ended December 31, 2025 (vs £0.7m in Q4 2024)
2025 net loss £29.4 million Year ended December 31, 2025 (vs £19.0m in 2024)
Warrant revaluation expense £12.6 million Non-cash finance expense for 2025 related to warrants
Share-based payments £10.0 million Share-based payment expenses for 2025 (vs £1.6m in 2024)

Previous Earnings Reports

5 past events · Latest: Nov 13 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Nov 13 Q3 2025 earnings Positive -2.3% Q3 2025 results, cash increase via ATM and financings, runway into 2029.
Aug 20 Q2 2025 earnings Positive +6.4% Q2 2025 results, expansion of NUC‑7738 study and major 2025 capital raise.
Jun 02 Q1 2025 earnings Positive +57.4% Q1 2025 results, reduced net loss and positive NUC‑7738 and NUC‑3373 data.
Mar 20 FY 2024 earnings Positive -2.2% Q4 and 2024 results, NUC‑7738 efficacy, improved loss and extended runway.
Nov 25 Q3 2024 earnings Positive +2.4% Q3 2024 results, promising NUC‑7738 and NUC‑3373 combination data.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings and business updates have often been clinically and financially constructive, but price reactions have been mixed, with both sharp rallies and modest declines following similar disclosures.

Recent Company History

Over recent earnings cycles, NuCana consistently paired financial updates with progress on NUC-7738 and NUC-3373. Cash runway disclosures extended from Q2 2025 into 2029 as the company raised capital and expanded its Phase 1/2 and Phase 2 studies. Prior earnings on Nov 13, 2025 and earlier quarters highlighted data in PD‑1 inhibitor‑resistant melanoma and combinations for NUC‑3373. Today’s 2025 year-end results continue that pattern, adding strengthened cash levels and clearer 2026 milestones.

Key Terms

pd-1 inhibitor-resistant melanoma, phase 2 expansion study, metastatic melanoma, complete metabolic response, +4 more
8 terms
pd-1 inhibitor-resistant melanoma medical
"NUC-7738 Demonstrates Clinical Activity and Favorable Safety in Patients with PD-1 Inhibitor-Resistant Melanoma"
PD-1 inhibitor-resistant melanoma is a form of skin cancer that no longer responds to a class of immune system drugs called PD-1 inhibitors, which are designed to help the body’s defenses recognize and attack tumor cells. For investors, resistance matters because it can reduce the value of existing therapies, change clinical trial prospects, and create demand for new drugs or combination treatments—similar to when a key no longer fits a lock and the market must find a new solution.
phase 2 expansion study medical
"Final Data from Phase 2 Expansion Study of NUC-7738 Expected in 2026"
A phase 2 expansion study is a clinical trial step where a treatment that showed initial promise is tested in more people to better understand its effectiveness and safety at a chosen dose. Think of it as widening a pilot program to see if early positive results hold up in a larger group; for investors, successful expansion can reduce technical risk, support higher valuation, and make the drug more likely to reach late-stage trials or attract partners.
metastatic melanoma medical
"evaluating NUC-7738 in combination with pembrolizumab in patients with PD-1 inhibitor-resistant metastatic melanoma"
A type of skin cancer that has spread from its original site to other organs or tissues in the body, making it more difficult to treat. For investors, it matters because the advanced stage changes expected treatment needs, clinical trial design, regulatory approval chances and potential market size for therapies — similar to how a problem that spreads beyond a single room requires a larger, more expensive solution than a localized issue.
complete metabolic response medical
"disease converted to a complete metabolic response with no detectable active disease"
A complete metabolic response is an imaging result, usually from a PET scan, showing no detectable abnormal metabolic activity from a disease — in cancer terms, it indicates that tumor cells are no longer lighting up on a metabolic “heat” scan. For investors, this outcome is a strong sign that a treatment is working at the cellular level and can influence clinical-readout value, regulatory decisions, and a company’s future revenue prospects, much like a fire that no longer shows on a heat sensor.
stable disease medical
"two partial responses, one confirmed, and multiple cases of stable disease"
Stable disease describes a situation in a clinical trial or treatment where a patient’s condition neither meaningfully improves nor worsens—tumors don’t shrink significantly but also don’t grow. For investors, this signal can matter because it shows a therapy may halt progression, which can support regulatory decisions, extend patient benefit and influence a drug’s commercial prospects; think of it as a stalled race where forward movement has paused but relapse hasn’t accelerated.
at-the-market program financial
"Subsequently, in July 2025, NuCana raised, through the at-the-market program, £19.0 million"
An at-the-market program is a way for a company to sell new shares of its stock gradually over time directly into the stock market, rather than all at once. This approach allows the company to raise money as needed while giving investors the opportunity to buy shares at current market prices. It helps manage the timing and price of new stock offerings, providing flexibility for both the company and investors.
warrants financial
"issued in the May 2025 financing, in exchange for payments totaling $3.6 million"
Warrants are special documents that give you the right to buy a company's stock at a set price before a certain date. They are often used as a way for companies to attract investors or raise money, and their value can increase if the company's stock price goes up.
View in glossary
share-based payment expenses financial
"Share-based payment expenses of £10.0 million (2024: £1.6 million); partly offset by"
Share-based payment expenses are the recorded costs a company recognizes when it compensates employees, consultants or suppliers with its own stock or stock-based instruments (like options or restricted shares) instead of cash. Investors care because these costs reduce reported profits and can increase the number of shares outstanding over time, diluting ownership and affecting metrics such as earnings per share and valuation—similar to a business paying wages with gift cards that change who owns part of the company.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

NUC-7738 Demonstrates Clinical Activity and Favorable Safety in Patients with PD-1 Inhibitor-Resistant Melanoma

Final Data from Phase 2 Expansion Study of NUC-7738 Expected in 2026

Advancing Additional Indications and Combination Strategies

Cash Runway Expected to Extend into 2029

EDINBURGH, United Kingdom, March 19, 2026 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA) (“NuCana” or the “Company”) today announced financial results for the fourth quarter and year ended December 31, 2025 and provided an update on its clinical development program with its two lead anti-cancer medicines.

“We are excited to enter 2026 with significant momentum as we continue to advance the development of our ProTide pipeline with the aim to deliver significantly improved treatment outcomes for patients with cancer,” said Hugh S. Griffith, NuCana’s Chief Executive Officer. “In late 2025, we presented compelling data from our Phase 2 NuTide:701 study at the annual European Society for Medical Oncology Immuno-Oncology Congress, evaluating NUC-7738 in combination with pembrolizumab in patients with PD-1 inhibitor-resistant metastatic melanoma. These data demonstrated a favorable safety profile and evidence of clinical activity, including two partial responses, one of which was confirmed, and multiple cases of stable disease, including one patient whose disease converted to a complete metabolic response with no detectable active disease.”

Mr. Griffith continued, “We expect to complete enrollment in the Phase 2 NuTide:701 expansion study in the first half of 2026, with final data expected later this year. We also plan to obtain regulatory guidance from the U.S. Food and Drug Administration regarding a potential registrational pathway for NUC-7738 in melanoma. In parallel, we are evaluating additional indications and combination strategies to further explore the therapeutic potential of NUC-7738.”

Mr. Griffith concluded, “Earlier this year we appointed Theresa Bruce as our Chief Operating Officer. Ms. Bruce brings over 25 years of oncology research and development experience, and her operational leadership will support the continued advancement of our pipeline. Based on our current operating plan, we expect our existing cash resources to fund operations into 2029, positioning us to execute on our key anticipated clinical and regulatory objectives.”

2026 Anticipated Milestones

  • NUC-7738
    • Complete patient recruitment in the Phase 2 expansion study (NuTide:701) evaluating NUC-7738 in combination with pembrolizumab in patients with PD-1 resistant melanoma;
    • Announce final data from the Phase 2 expansion study (NuTide:701) of NUC-7738 in combination with pembrolizumab in patients with PD-1 resistant melanoma;
    • Obtain regulatory guidance from the U.S. Food and Drug Administration regarding a potential registrational strategy for NUC-7738 in melanoma; and
    • Advance evaluation of additional indications and combination strategies.
  • NUC-3373
    • Evaluate optimal combinations and indications to inform potential future clinical studies of NUC-3373.

Fourth Quarter and Year-End 2025 Financial Highlights and Cash Position

As at December 31, 2025, NuCana had cash and cash equivalents of £24.3 million compared to £25.2 million at September 30, 2025 and £6.7 million at December 31, 2024.

In May 2025, NuCana completed a financing, raising £9.6 million in gross proceeds, £5.2 million upfront and £4.4 million from the exercise of warrants, before expenses and commissions.

Subsequently, in July 2025, NuCana raised, through the at-the-market program, £19.0 million in gross proceeds before expenses and commissions. On July 21, 2025, having raised the full amount of capital required, NuCana announced it had successfully canceled all remaining Series A Warrants issued in the May 2025 financing, in exchange for payments totaling $3.6 million. This initiative fully eliminated all overhanging rights from the May 2025 financing.

NuCana anticipates its cash and cash equivalents at December 31, 2025 will be sufficient to fund its planned operations into 2029.

NuCana reported a net loss of £2.5 million for the quarter ended December 31, 2025, as compared to a net loss of £0.7 million for the quarter ended December 31, 2024. Basic and diluted loss per ordinary share was £0.00 for the quarter ended December 31, 2025, as compared to a loss per ordinary share of £0.01 for the comparable quarter ended December 31, 2024.

NuCana reported a net loss of £29.4 million for the year ended December 31, 2025, as compared to a net loss of £19.0 million for the year ended December 31, 2024. The net loss for the year ended December 31, 2025 included the following non-cash or non-recurring items:

  • Finance expense of £12.6 million (2024: £nil) relating to the non-cash loss on fair value revaluation of the warrants issued in the May 2025 financing;
  • Professional fees of £1.4 million (2024: £nil) related to the issue of warrants; and
  • Share-based payment expenses of £10.0 million (2024: £1.6 million); partly offset by
  • Total other income of £2.7 million (2024: £nil).

Basic and diluted loss per ordinary share was £0.00 for the year ended December 31, 2025, as compared to a loss per ordinary share of £0.26 for the year ended December 31, 2024.

About NuCana

NuCana is a clinical-stage biopharmaceutical company focused on significantly improving treatment outcomes for patients with cancer by applying our ProTide technology to transform some of the most widely prescribed chemotherapy agents, nucleoside analogs, into more effective and safer medicines. While these conventional agents remain part of the standard of care for the treatment of many solid and hematological tumors, they have significant shortcomings that limit their efficacy and they are often poorly tolerated. Utilizing our proprietary technology, we are developing new medicines, ProTides, designed to overcome the key limitations of nucleoside analogs and generate much higher concentrations of anti-cancer metabolites in cancer cells. NuCana’s pipeline includes NUC-7738 and NUC-3373. NUC-7738 is a novel anti-cancer agent that disrupts RNA polyadenylation, profoundly impacts gene expression in cancer cells and targets multiple aspects of the tumor microenvironment. NUC-7738 is in the Phase 2 part of a Phase 1/2 study which is evaluating NUC-7738 as a monotherapy in patients with advanced solid tumors and in combination with pembrolizumab in patients with melanoma. NUC-3373 is a targeted thymidylate synthase (“TS”) inhibitor designed to overcome key pharmacological limitations associated with other TS inhibitors. NUC-3373 has recently been evaluated in a Phase 1b/2 modular study (NuTide:303) of NUC-3373 in combination with the PD-1 inhibitor pembrolizumab for patients with advanced solid tumors and in combination with docetaxel for patients with lung cancer, and NuCana is currently evaluating further characterization of mode of action and target indications for further clinical studies of NUC-3373.

Forward-Looking Statements
This press release may contain “forward-looking” statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are based on the beliefs and assumptions and on information currently available to management of the Company. All statements other than statements of historical fact contained in this press release are forward-looking statements, including statements concerning the Company’s planned and ongoing clinical studies for the Company’s product candidates and the potential advantages of those product candidates, including NUC-7738 and NUC-3373; the initiation, enrollment, timing, progress, release of data from and results of those planned and ongoing clinical studies; the Company’s goals with respect to the development, regulatory pathway and potential use, if approved, of each of its product candidates; the utility of prior non-clinical and clinical data in determining future clinical results; and the sufficiency of the Company’s current cash and cash equivalents to fund its planned operations into 2029. In some cases, you can identify forward-looking statements by terminology such as “may,” “will,” “should,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “predicts,” “potential” or “continue” or the negative of these terms or other comparable terminology. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the Company’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These risks and uncertainties include, but are not limited to, our ability to raise additional capital sufficient to fund our planned operations and the risks and uncertainties set forth in the “Risk Factors” section of the Company’s Annual Report on Form 20-F for the year ended December 31, 2025 filed with the Securities and Exchange Commission (“SEC”) on March 19, 2026, and subsequent reports that the Company files with the SEC. Forward-looking statements represent the Company’s beliefs and assumptions only as of the date of this press release. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, it cannot guarantee future results, levels of activity, performance or achievements. Except as required by law, the Company assumes no obligation to publicly update any forward-looking statements for any reason after the date of this press release to conform any of the forward-looking statements to actual results or to changes in its expectations.

Condensed Consolidated Statements of Operations

  For the Three Months Ended
December 31,
 For the Year Ended
December 31,
  2025  2024  2025  2024 
  (in thousands, except per share data)
  (unaudited)   
  £  £  £  £ 
             
Research and development expenses (1,736) (729) (12,737) (18,017)
Administrative expenses (1,107) (540) (8,096) (4,988)
Impairment of intangible assets -  (33) -  (33)
Other income -  -  841  - 
Net foreign exchange gains (losses) 43  437  (118) 229 
Operating loss (2,800) (865) (20,110) (22,809)
Other income -  -  1,851  - 
Finance income 173  75  386  358 
Finance expense -  -  (12,648) - 
Loss before tax (2,627) (790) (30,521) (22,451)
Income tax credit 142  137  1,168  3,454 
Loss for the period attributable to equity holders of the Company (2,485) (653) (29,353) (18,997)
         
Basic and diluted loss per ordinary share (0.00) (0.01) (0.00) (0.26)
             

Condensed Consolidated Statements of Financial Position As At

  December 31,
2025
 December 31,
2024

  (in thousands)
  £ £
Assets    
Non-current assets    
Intangible assets 2,198  2,199 
Property, plant and equipment 658  197 
Deferred tax asset 117  113 
  2,973  2,509 
Current assets    
Prepayments, accrued income and other receivables 849  922 
Current income tax receivable 1,761  4,594 
Cash and cash equivalents 24,251  6,749 
  26,861  12,265 
Total assets 29,834  14,774 
     
Equity and liabilities    
Capital and reserves    
Share capital and share premium 189,586  151,827 
Other reserves 87,075  78,421 
Accumulated deficit (252,334) (224,294)
Total equity attributable to equity holders of the Company 24,327  5,954 
     
Non-current liabilities    
Provisions 58  37 
Lease liabilities 656  117 
  714  154 
Current liabilities    
Trade payables 522  2,705 
Payroll taxes and social security 99  134 
Accrued expenditure 4,152  5,714 
Lease liabilities 20  73 
Provisions -  40 
  4,793  8,666 
Total liabilities 5,507  8,820 
Total equity and liabilities 29,834  14,774 
     

Condensed Consolidated Statements of Cash Flows

 For the Year Ended
December 31,
 2025
 2024
 (in thousands)
 £ £
Cash flows from operating activities   
Loss for the period(29,353) (18,997)
Adjustments for:   
Income tax credit(1,168) (3,454)
Amortization and depreciation274  522 
Impairment of intangible assets-  33 
Movement in provisions(40) 10 
Finance income(386) (358)
Finance expense12,648  - 
Interest expense on lease liabilities20  17 
Share-based payments10,028  1,646 
Net foreign exchange losses (gains)194  (369)
 (7,783) (20,950)
Movements in working capital:   
Decrease in prepayments, accrued income and other receivables109  1,737 
Decrease in trade payables(2,183) (670)
Decrease in payroll taxes, social security and accrued expenditure(1,598) (3,250)
Movements in working capital(3,672) (2,183)
Cash used in operations(11,455) (23,133)
Net income tax received3,988  4,015 
Net cash used in operating activities(7,467) (19,118)
Cash flows from investing activities   
Interest received352  372 
Payments for property, plant and equipment-  (4)
Payments for intangible assets(193) (289)
Net cash from investing activities159  79 
Cash flows from financing activities   
Payments for lease liabilities(54) (223)
Proceeds from exercise of share options1  7 
Proceeds from issue of share capital20,185  8,729 
Proceeds from exercise of warrants4,436  - 
Proceeds from issue of warrants4,439  - 
Payment for cancellation of warrants(2,655) - 
Share issue expenses(1,346) (329)
Net cash from financing activities25,006  8,184 
Net increase (decrease) in cash and cash equivalents17,698  (10,855)
Cash and cash equivalents at beginning of period6,749  17,225 
Effect of exchange rate changes on cash and cash equivalents(196) 379 
Cash and cash equivalents at end of period24,251  6,749 
    

For more information, please contact:

NuCana plc
Hugh S. Griffith
Chief Executive Officer
+44 131-357-1111
info@nucana.com

ICR Healthcare
Chris Brinzey
+1 339-970-2843
Chris.Brinzey@ICRHealthcare.com


FAQ

What clinical results did NuCana (NCNA) report for NUC-7738 in PD-1 resistant melanoma?

NUC-7738 demonstrated clinical activity and a favorable safety profile in PD-1 resistant melanoma patients. According to the company, the Phase 2 expansion showed two partial responses (one confirmed) and multiple stable disease cases, including one patient converting to a complete metabolic response.

When does NuCana expect final Phase 2 NuTide:701 data for NUC-7738 (NCNA)?

NuCana expects to announce final Phase 2 NuTide:701 expansion data in 2026. According to the company, enrollment should complete in the first half of 2026, with final data reported later in the year and regulatory engagement with the FDA planned thereafter.

How long is NuCana's (NCNA) cash runway after the 2025 financings?

NuCana expects existing cash to fund operations into 2029 based on its current plan. According to the company, cash and cash equivalents were £24.3M at December 31, 2025, following gross 2025 financings totaling £28.6M before expenses and commissions.

What were NuCana's (NCNA) key 2025 financial results and notable expenses?

NuCana reported a 2025 net loss of £29.4M, up from £19.0M in 2024. According to the company, this included a £12.6M non-cash finance expense for warrant revaluation and £10.0M in share-based payment expense.

What near-term regulatory and development milestones has NuCana (NCNA) outlined for 2026?

NuCana plans to complete NuTide:701 enrollment, release final expansion data, and seek FDA guidance on a registrational pathway in 2026. According to the company, it will also evaluate additional indications and combination strategies for NUC-7738 and progress NUC-3373 combination studies.