NCNA NuCana plc Sponsored ADR

NuCana Reports Third Quarter 2022 Financial Results and Provides Business Update

NuCana Reports Third Quarter 2022 Financial Results and Provides Business Update

Multiple Data Readouts on Track for the Remainder of 2022 and the First Half of 2023

Well Capitalized with Anticipated Cash Runway into 2025

EDINBURGH, United Kingdom, Nov. 16, 2022 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA) announced financial results for the third quarter ended September 30, 2022 and provided an update on its broad clinical program with its transformative ProTide therapeutics.

As of September 30, 2022, NuCana had cash and cash equivalents of £50.8 million compared to £46.5 million as of June 30, 2022 and £60.3 million at December 31, 2021. NuCana continues to advance its various clinical programs and reported a net loss of £4.5 million for the quarter ended September 30, 2022, as compared to a net loss of £8.0 million for the quarter ended September 30, 2021. Basic and diluted loss per share was £0.09 for the quarter ended September 30, 2022, as compared to £0.15 per share for the quarter ended September 30, 2021.

“This year we have focused on advancing our transformative ProTides through the clinic and evaluating additional indications and combinations to expand our development program,” said Hugh S. Griffith, NuCana’s Founder and Chief Executive Officer. “Based on NUC-3373’s promising efficacy and favorable safety profile, we initiated two clinical studies: NuTide:323, a randomized Phase 2 trial of NUC-3373 in combination with irinotecan (NUFIRI) and bevacizumab for the second-line treatment of patients with colorectal cancer; and NuTide:303 a Phase 1b/2 study of NUC-3373 in combination with either pembrolizumab in patients with solid tumors or in combination with docetaxel in patients with non-small cell lung cancer (NSCLC). Furthermore, we entered the Phase 2 part of the NuTide:701 study which is investigating NUC-7738 as a monotherapy and in combination with pembrolizumab in patients with solid tumors.”

Mr. Griffith continued: “We recently presented data at the European Society of Medical Oncology (ESMO) Annual Meeting that showed the promising anti-tumor activity and favorable safety profiles of both NUC-3373 and NUC-7738. We presented encouraging data for NUC-3373 in combination with irinotecan (NUFIRI) or oxaliplatin (NUFOX) from the NuTide:302 Phase 1b/2 study in patients with advanced colorectal cancer. We also presented positive data on NUC-7738 in patients with solid tumors, including melanoma, from the Phase 1 part of the Phase 1/2 NuTide:701 study. At the 34th EORTC-NCI-AACR Annual Meeting in October, we presented data demonstrating that NUC-3373 is a more potent inhibitor of thymidylate synthase than pemetrexed in both adenocarcinoma and squamous subtypes of NSCLC. In addition, we presented data that demonstrate NUC-3373’s ability to increase the immunogenic cell death of lung cancer cells in combination with pembrolizumab.”

Mr. Griffith concluded: “We are pleased with the progress we have made this year with NUC-3373 and NUC-7738. Based on these positive data updates, we have expanded our development programs and are rapidly advancing them as we progress towards our goal of providing more effective and safer treatment options for patients with cancer. With a cash runway that is expected to fund operations into 2025, we look forward to achieving numerous value-driving catalysts in the near future.”

Anticipated Milestones: Q4 2022 and H1 2023

•  NUC-3373 (a ProTide transformation of 5-FU)

In Q4 2022, NuCana expects to:

  • Commence enrollment in the randomized, controlled Phase 2 (NuTide:323) study of NUC-3373 in combination with other agents for the second-line treatment of patients with colorectal cancer;
  • Commence enrollment in the Phase 1b/2 (NuTide:303) modular study of NUC-3373 in combination with either pembrolizumab in patients with various solid tumors or in combination with docetaxel in patients with non-small cell lung cancer (NSCLC) to identify additional indications for development; and
  • Expand the Phase 1b/2 (NuTide:302) study of NUC-3373 in colorectal cancer patients, and evaluate NUC-3373-based regimens in combination with bevacizumab in second-line patients with colorectal cancer.

In the first half of 2023, NuCana expects to:

  • Announce data from the Phase 1b/2 (NuTide:302) study of NUC-3373 combined with leucovorin, bevacizumab and either irinotecan or oxaliplatin in second-line patients with colorectal cancer; and
  • Announce data from the Phase 1b/2 (NuTide:303) modular study of NUC-3373 in combination with either pembrolizumab in patients with various solid tumors or docetaxel in patients with non-small cell lung cancer (NSCLC) to identify additional indications for development.

•  NUC-7738 (a ProTide transformation of 3’-deoxyadenosine)

In Q4 2022, NuCana expects to:

  • Commence enrollment in the Phase 2 part of the NuTide:701 study of NUC-7738 in combination with the PD-1 inhibitor pembrolizumab, in patients with solid tumors; and

  • Announce data from the Phase 2 part of the NuTide:701 study in patients with solid tumors treated with NUC-7738 monotherapy.

In the first half of 2023, NuCana expects to:

  • Announce data from the Phase 1 part of the NuTide:701 study of NUC-7738 in patients with solid tumors; and
  • Announce data from the Phase 2 part of the NuTide:701 study in patients with solid tumors treated with NUC-7738 monotherapy and NUC-7738 in combination with pembrolizumab.

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-3373 and NUC-7738. NUC-3373 is a new chemical entity derived from the nucleoside analog 5-fluorouracil, a widely used chemotherapy agent. NUC-3373, in combination with other agents, is in a Phase 1b/2 study in patients with metastatic colorectal cancer. NuCana has also initiated a randomized Phase 2 study of NUC-3373, in combination with other agents, for the second-line treatment of patients with advanced colorectal cancer. In addition, NuCana has initiated a Phase 1b/2 modular study of NUC-3373 in combination with other agents, including the PD-1 inhibitor pembrolizumab, in patients with advanced solid tumors to identify additional indications for development. NUC-7738 is a transformation of 3’-deoxyadenosine, a novel anti-cancer nucleoside analog. NUC-7738 is in the Phase 2 part of a Phase 1/2 study in patients with advanced solid tumors which is evaluating NUC-7738 as a monotherapy and in combination with pembrolizumab.

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 NuCana plc (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-3373 and NUC-7738; 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, cash equivalents and marketable securities to fund its planned operations into 2025. 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, 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, 2021 filed with the Securities and Exchange Commission (“SEC”) on April 27, 2022, 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.

 
Unaudited Condensed Consolidated Statements of Operations
     
  For the Three Months Ended

 For the Nine Months Ended

  September 30, September 30,
  2022  2021

 2022 2021

  (in thousands, except per share data)
  £  £  £  £ 
Research and development expenses (7,386) (8,971) (23,238) (26,200)
Administrative expenses (1,715) (2,277) (5,756) (6,456)
Net foreign exchange gains 2,912  1,274  7,120  488 
Operating loss (6,189) (9,974) (21,874) (32,168)
Finance income 216  22  380  81 
Loss before tax (5,973) (9,952) (21,494) (32,087)
Income tax credit 1,445  1,911  4,672  5,198 
Loss for the period (4,528) (8,041) (16,822) (26,889)
       
Basic and diluted loss per share (0.09) (0.15) (0.32) (0.52)
             



Unaudited Condensed Consolidated Statements of Financial Position
    
  September 30,

2022

 December 31,

2021


      
  (in thousands)

  £  £ 
Assets      
Non-current assets      
Intangible assets 2,512  2,410 
Property, plant and equipment 969  851 
Deferred tax asset 95  60 
Other non-current assets 2,655  2,540 
  6,231  5,861 
Current assets      
Prepayments, accrued income and other receivables 7,052  4,161 
Current income tax receivable 4,622  7,188 
Cash and cash equivalents 50,752  60,264 
  62,426  71,613 
Total assets 68,657  77,474 
       
Equity and liabilities      
Capital and reserves      
Share capital and share premium 143,138  143,137 
Other reserves 75,068  72,137 
Accumulated deficit (165,513) (149,726)
Total equity attributable to equity holders of the Company 52,693  65,548 
       
Non-current liabilities      
Provisions 46  46 
Lease liabilities 459  164 
  505  210 
Current liabilities      
Trade payables 5,614  1,829 
Payroll taxes and social security 166  170 
Accrued expenditure 9,456  9,510 
Lease liabilities 223  207 
  15,459  11,716 
Total liabilities 15,964  11,926 
Total equity and liabilities 68,657  77,474 
       



Unaudited Condensed Consolidated Statements of Cash Flows
 
 For the Nine Months Ended September 30,

 
 2022

  2021

 
 (in thousands)

 £  £ 
Cash flows from operating activities     
Loss for the period(16,822) (26,889)
Adjustments for:     
Income tax credit(4,672) (5,198)
Amortization, depreciation and loss on disposal676  673 
Finance income(380) (81)
Interest expense on lease liabilities11  15 
Share-based payments3,900  4,919 
Net foreign exchange gains(7,233) (533)
 (24,520) (27,094)
Movements in working capital:     
Increase in prepayments, accrued income and other receivables(2,758) (497)
Increase in trade payables3,785  1,634 
(Decrease) increase in payroll taxes, social security and accrued expenditure(101) 2,333 
Movements in working capital926  3,470 
Cash used in operations(23,594) (23,624)
Net income tax received7,220  9,888 
Net cash used in operating activities(16,374) (13,736)
Cash flows from investing activities     
Interest received368  79 
Payments for property, plant and equipment(12) (43)
Payments for intangible assets(396) (537)
Payments for other non-current assets-  (2,597)
Net cash used in investing activities(40) (3,098)
Cash flows from financing activities     
Payments for lease liabilities(189) (222)
Proceeds from issue of share capital1  198 
Net cash used in financing activities(188) (24)
Net decrease in cash and cash equivalents(16,602) (16,858)
Cash and cash equivalents at beginning of period60,264  87,356 
Effect of exchange rate changes on cash and cash equivalents7,090  529 
Cash and cash equivalents at end of period50,752  71,027 
      

For more information, please contact:

NuCana plc

Hugh S. Griffith

Chief Executive Officer

1

 

Westwicke, an ICR Company

Chris Brinzey



 

RooneyPartners

Marion Janic



 



EN
16/11/2022

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on NuCana plc Sponsored ADR

 PRESS RELEASE

NuCana Reports First Quarter 2025 Financial Results and Provides Busin...

NuCana Reports First Quarter 2025 Financial Results and Provides Business Update Initiation of Expansion Study of NUC-7738 in Combination with Pembrolizumab for Patients with PD-1 Inhibitor-Resistant Melanoma Initial Data from the Expansion Study of NUC-7738 Expected in Q4 2025 with Final Data in 2026 Additional Data from the Ongoing Phase 1b/2 Study of NUC-3373 in Combination with Pembrolizumab Remain on track for 2025 Anticipated Cash Runway Extended into Q4 2026 to Support Key Value-Driving Milestones and Complete the Expansion Study of NUC-7738 EDINBURGH, United Kingdom, Jun...

 PRESS RELEASE

NuCana Prices $7 Million Registered Direct Offering

NuCana Prices $7 Million Registered Direct Offering EDINBURGH, United Kingdom, May 06, 2025 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA), a clinical-stage biopharmaceutical company that focuses on significantly improving treatment outcomes for patients with cancer, announced that it has priced a registered direct offering consisting of 10,845,985 American Depository Shares, or ADSs, (or pre-funded warrants in lieu thereof) with each ADS (or pre-funded warrant) accompanied by (i) a Series A warrant to purchase one (1) ADS at an initial exercise price of $0.8068 per share and (ii) a Series...

 PRESS RELEASE

NuCana Reports Fourth Quarter and Year-End 2024 Financial Results and ...

NuCana Reports Fourth Quarter and Year-End 2024 Financial Results and Provides Business Update Remains on Track to Initiate an Expansion Study of NUC-7738 in Combination with Pembrolizumab for Patients with PD-1 Inhibitor-Resistant Melanoma in 2025 Data from the Expansion Study to Support Interaction with FDA and Define Regulatory Strategy for NUC-7738 Data from the Ongoing Phase 1b/2 Study of NUC-3373 in Combination with Pembrolizumab Anticipated Cash Runway Extended into Q3 2025 EDINBURGH, United Kingdom, March 20, 2025 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA) announced financi...

 PRESS RELEASE

NuCana Reports Third Quarter 2024 Financial Results and Provides Busin...

NuCana Reports Third Quarter 2024 Financial Results and Provides Business Update Presented Encouraging Phase 2 Data on NUC-7738 in Combination with Pembrolizumab at the European Society for Medical Oncology (ESMO) Congress 2024 Announced Promising Phase 1b/2 Data on NUC-3373 in Combination with Pembrolizumab or Docetaxel Anticipated Cash Runway into Q2 2025 EDINBURGH, United Kingdom, Nov. 25, 2024 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA) announced financial results for the third quarter ended September 30, 2024 and provided an update on its clinical development program with its tw...

 PRESS RELEASE

NuCana Announces Encouraging Initial Data from Phase 1b/2 Modular Stud...

NuCana Announces Encouraging Initial Data from Phase 1b/2 Modular Study of NUC-3373 in Combination with Pembrolizumab or Docetaxel Patients with Advanced Solid Tumors who had Exhausted All Other Treatment Options and were PD-(L)1 Experienced Achieved Significant Tumor Volume Reductions and Prolonged Progression Free Survival Following Treatment with NUC-3373 plus Pembrolizumab One Patient Achieved a 100% Reduction in their Target Lesion Patients with Lung Cancer who had Exhausted All Other Treatment Options Achieved Prolonged Progression Free Survival Following Treatment with NUC-3373 plu...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch