Cue Biopharma Reports Fourth Quarter and Full Year 2024 Financial Results and Business Highlights

March 31, 2025 16:20 ET | Source: Cue Biopharma, Inc. BOSTON, March 31, 2025 (GLOBE NEWSWIRE) -- - Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company developing a novel class of therapeutic biologics to selectively engage and modulate disease-specific T cells for the treatment of cancer and autoimmune disease, today reported fourth quarter and full year 2024 financial results. Prioritized resources on potentially disruptive autoimmune programs while enabling maturation of clinical data from oncology programs to further support prospective strategic partnershipsAppointed key industry leaders to management team and board of directors Lucinda Warren, Chief Business OfficerIndustry veteran, with extensive experience and proven expertise in strategic transactions, portfolio optimization and alliance managementDaniel Baker, M.D., Interim Chief Development OfficerOver 20 years of drug development experience in the pharmaceutical industryPasha Sarraf, M.D., Ph.D., Member of Board of Directors Physician-scientist with extensive experience in the business of science and biotechnology Successfully regained worldwide development and commercialization rights for CUE-401, the Company’s lead autoimmune program with potential to transform treatment across a broad spectrum of autoimmune and inflammatory diseasesAdvanced research and development of CUE-501 as lead program of the CUE-500 series, demonstrating the potential to harness anti-viral specific T cells against pathogenic cells in both autoimmune and oncologyCompany plans to announce business update call and webcast within the next couple of weeks “During 2024 and Q1 2025, we made significant progress shaping the company for success,” said Daniel Passeri, chief executive officer of Cue Biopharma. “We believe that the ongoing advancement of our prioritized autoimmune programs and the implementation of a highly focused strategic business model, support our ability to exploit the potentially disruptive opportunity of our Immuno-STAT™ platform, specifically CUE-401.” Fourth Quarter 2024 Financial Results The Company reported collaboration revenue of $1.6 million and $1.8 million for the three months ended December 31, 2024 and 2023, respectively. The decrease was due to revenue earned from the strategic collaboration agreement entered into with Ono Pharmaceutical in the first quarter of 2023. Research and development expenses were $7.2 million and $10.9 million for the three months ended December 31, 2024 and 2023, respectively. The decrease was primarily due to decreases in both drug substance manufacturing and clinical trial costs. General and administrative expenses were $4.0 million and $4.6 million for the three months ended December 31, 2024 and 2023, respectively. The decrease was primarily due to a decrease in professional fees. Full Year 2024 Financial Results The Company reported collaboration revenue of $9.3 million and $5.5 million for the years ended December 31, 2024 and 2023, respectively. The increase was due to revenue earned from our strategic collaboration agreement entered into with Ono Pharmaceutical in the first quarter of 2023. Research and development expenses were $36.3 million and $40.8 million for the years ended December 31, 2024 and 2023, respectively. The decrease was primarily due to decreases in clinical trial costs, employee compensation, which includes stock-based compensation, and manufacturing costs. General and administrative expenses were $14.6 million and $16.7 million for the years ended December 31, 2024 and 2023, respectively. The decrease was primarily due to decreases in employee compensation, which includes stock-based compensation, and professional fees. As of December 31, 2024, the Company had $22.5 million in cash and cash equivalents. Cue Biopharma, Inc.Consolidated Statements of Operations and Comprehensive Loss(In thousands, except share and per share amounts) Three Months EndedDecember 31, Year EndedDecember 31, 2024 2023 2024 2023 Collaboration revenue$1,576 $1,821 $9,287 $5,490 Operating expenses (income): General and administrative 4,021 4,609 14,585 16,680 Research and development 7,184 10,887 36,295 40,802 Loss (gain) on fixed asset disposal 4 157 (93) 157 Total operating expenses 11,209 15,653 50,787 57,639 Loss from operations$(9,633) $(13,832) $(41,500) $(52,149)Other income (expense): Interest income 290 905 1,622 2,661 Interest expense (153) (507) (796) (1,245)Total other income, net 137 398 826 1,416 Net loss$(9,496) $(13,434) $(40,674) $(50,733)Unrealized gain from available-for-sale securities - - - 96 Comprehensive loss (9,496) (13,434) (40,674) (50,637)Net loss per common share – basic and diluted$(0.13) $(0.28) $(0.72) $(1.11)Weighted average common shares outstanding – basic and diluted 74,238,329 47,181,633 56,328,348 45,754,794 Cue Biopharma, Inc.Consolidated Balance Sheets(In thousands) December 31, 2024 December 31, 2023 Assets Cash and cash equivalents$22,459 $48,514 Other assets 9,732 13,016 Total assets$32,191 $61,530 Liabilities and stockholders’ equity Liabilities$14,692 $24,445 Stockholders' equity 17,499 37,085 Total Liabilities and stockholders’ equity$32,191 $61,530 About Cue BiopharmaCue Biopharma, a clinical-stage biopharmaceutical company, is developing a novel class of injectable biologics to selectively engage and modulate disease-specific T cells directly within the patient’s body. The company’s proprietary platform, Immuno-STAT™ (Selective Targeting and Alteration of T cells) and biologics are designed to harness the curative potential of the body’s intrinsic immune system through the selective modulation of disease-specific T cells without the adverse effects of broad systemic immune modulation. Headquartered in Boston, Massachusetts, we are led by an experienced management team with deep expertise in immunology and protein engineering as well as the design and clinical development of protein biologics. For more information please visit www.cuebiopharma.com and follow us on X and LinkedIn. Cautionary Note Regarding Forward-Looking StatementsThis press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, those regarding: the company’s belief that CUE-401 has potential to transform treatment across a broad spectrum of autoimmune and inflammatory diseases; the potential therapeutic benefits of CUE-501 and the CUE-500 series; the company’s ability to advance its Immuno-STAT™ platform; and the company’s business strategies, plans and prospects. Forward-looking statements, which are based on certain assumptions and describe the company’s future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as “believe,” “expect,” “may,” “will,” “should,” “would,” “could,” “seek,” “intend,” “plan,” “goal,” “project,” “estimate,” “anticipate,” “strategy,” “future,” “likely” or other comparable terms, although not all forward-looking statements contain these identifying words. All statements other than statements of historical facts included in this press release regarding the company’s strategies, prospects, financial condition, operations, costs, plans and objectives are forward-looking statements. Important factors that could cause the company’s actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others, the company’s limited operating history, limited cash and a history of losses; the company’s ability to obtain adequate financing to fund its business operations in the near term and successfully remediate its current “going concern” determination that it does not have sufficient capital on hand to continue operations beyond the next twelve months; the company’s ability to achieve profitability; potential setbacks in the company’s research and development efforts including negative or inconclusive results from its preclinical studies or clinical trials or the company’s ability to replicate in later clinical trials positive results found in preclinical studies and early-stage clinical trials of its product candidates; serious and unexpected drug-related side effects or other safety issues experienced by participants in clinical trials; its ability to secure required U.S. Food and Drug Administration (“FDA”) or other governmental approvals for its product candidates and the breadth of any approved indication; adverse effects caused by public health pandemics, including possible effects on the company’s operations and clinical trials; delays and changes in regulatory requirements, policy and guidelines including potential delays in submitting required regulatory applications to the FDA; the company’s reliance on licensors, collaborators, contract research organizations, suppliers and other business partners; the company’s ability to maintain and enforce necessary patent and other intellectual property protection; competitive factors; general economic and market conditions and the other risks and uncertainties described in the Risk Factors and Management's Discussion and Analysis of Financial Condition and Results of Operations sections of the company’s most recently filed Annual Report on Form 10-K and any subsequently filed Quarterly Report(s) on Form 10-Q. Any forward-looking statement made by the company in this press release is based only on information currently available to the company and speaks only as of the date on which it is made. The company undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise. Investor Contact Marie Campinell Senior Director, Corporate CommunicationsCue Biopharma, Inc.mcampinell@cuebio.com Media ContactJonathan PappasLifeSci Communicationsjpappas@lifescicomms.com

Cue Biopharma Reports Fourth Quarter and Full Year 2024 Financial Results and Business Highlights

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