Cue Biopharma Reports Second Quarter 2026 Financial Results and Recent Business Highlights
Rhea-AI Summary
Cue Biopharma (Nasdaq:CUE) reported second quarter 2026 collaboration revenue of $7.9 million, up from $3.0 million a year earlier, primarily from a Boehringer Ingelheim preclinical milestone. Operating expenses rose sharply, with R&D at $49.0 million and G&A at $46.6 million, driven largely by one-time cash and non-cash items related to the CUE-221 license from Ascendant and a strategic transformation.
Other expense included a substantial non-cash loss tied to liability-classified warrants, leading to a net loss of $153.1 million versus $8.5 million in 2025. Cash and equivalents were $17.4 million at June 30, 2026, with a subsequent $50 million private placement completed. Cue submitted an IND for CUE-221 in food allergy, expects Phase 2 data in chronic spontaneous urticaria by end of Q3 2026, and plans to initiate a CUE-401 Phase 1 study by year-end. The company also added a new CMO/Head of R&D and CFO.
Positive
- Collaboration revenue $7.9M in Q2 2026 vs. $3.0M in 2025
- $50M private placement completed after June 30, 2026
- CUE-221 IND submitted to FDA for food allergy applications
- Boehringer Ingelheim milestone revenue recognized in Q2 2026
- New CMO/Head of R&D and CFO appointed to strengthen leadership
Negative
- R&D expenses $49.0M in Q2 2026 vs. $7.9M in 2025
- G&A expenses $46.6M in Q2 2026 vs. $3.7M in 2025
- Net loss $153.1M in Q2 2026 vs. $8.5M in 2025
- Total operating expenses $95.6M in Q2 2026 vs. $11.6M in 2025
- Cash and equivalents $17.4M at June 30, 2026 before PIPE proceeds
- Loss on liability-classified warrants $90.0M, partly offset by $24.5M fair value gain
News Explained
The completed
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| May 14 | Q1 earnings report | Positive | -9.2% | Revenue growth, reduced loss, CUE-221 licensing, and $30 million financing highlighted quarter. |
| Mar 16 | Q4 earnings report | Positive | -12.8% | ImmunoScape collaboration, financing actions, full-year results, and pipeline progress drove announcement. |
| Nov 12 | Q3 earnings report | Positive | -7.2% | ImmunoScape deal, clinical response data, and leadership transition shaped results. |
| Aug 12 | Q2 earnings report | Positive | +2.6% | Boehringer collaboration, clinical results, and public offering accompanied quarterly results. |
| May 12 | Q1 earnings report | Positive | +2.3% | Boehringer collaboration, follow-on offering, and CUE-401 rights recovery accompanied results. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Tag-matched earnings events averaged -4.87%, with negative reactions following the three most recent reports and positive reactions in the two 2025 comparisons.
Key Terms
investigational new drug regulatory
private placement financial
phase 2 medical
anti-IgE antibody medical
liability-classified warrants financial
AI-generated analysis. How Rhea-AI works. Not financial advice.
- Announced recent Investigational New Drug (IND) submission to the FDA for CUE-221 in food allergy applications
- Completed a
$50 million private placement (PIPE) to further fund clinical development and the portfolio with significant potential for value-inflection - Strengthened the leadership team with the appointments of the Chief Medical Officer and Head of R&D and the Chief Financial Officer
- Operating results reflected higher expenditures related to the licensing and initiation of the CUE-221 development program, driven by one-time non-cash charges and acquisition-related payments
BOSTON, Aug. 14, 2026 (GLOBE NEWSWIRE) -- Cue Biopharma, Inc. (Nasdaq: CUE), a clinical stage biopharmaceutical company targeting transformative therapies for immune-mediated diseases, today reported second quarter 2026 financial results as well as recent business highlights.
“I am pleased with our progress this quarter, advancing our pipeline and strengthening our position for long-term growth,” said Shao-Lee Lin, M.D., Ph.D., president and chief executive officer of Cue Biopharma. “The CUE-221 license agreement augments our portfolio and opportunities and the higher expenditures this quarter reflect expected one-time non-cash items and payments related to the transaction. Combined with our recent CUE-221 IND submission, financing with high-quality investors, and strategic leadership additions, we believe we are well positioned for the next phase of execution. We look forward to anticipated CUE-221 Phase 2 data by the end of this quarter and remain on track to initiate a CUE-401 Phase 1 study by the end of the year.”
Business, Financial and Leadership Highlights
Milestones
CUE-221
- Recently submitted an IND to the FDA in food allergy applications
- Phase 2 data readout in Chronic Spontaneous Urticaria anticipated by the end of the third quarter of 2026
CUE-401
- Company anticipates submitting an IND to the FDA and initiating a Phase 1 clinical study by year-end 2026
Financial and Corporate
- Completed a private placement for gross proceeds of
$50 million primarily to support clinical development, pipeline advancement, and infrastructure growth
Leadership
- Dr. Dominic Borie, Chief Medical Officer and Head of Research and Development, physician-scientist and immunology leader with deep expertise in immunology, joined Cue to help advance key clinical programs in allergic and autoimmune diseases
- Mr. James M. Ahlers, Chief Financial Officer, a veteran biotechnology finance executive, joined Cue to help strengthen the Company’s financial leadership and the infrastructure needed to support execution of its corporate strategy
Second Quarter 2026 Financial Results
Second quarter revenue was
Research and development expenses were
General and administrative expenses were
Other income and expense for the three months ended June 30, 2026, primarily comprised a net non-cash loss of
Net loss for the three months ended June 30, 2026 was
As of June 30, 2026, the Company had
| Cue Biopharma, Inc. Condensed Consolidated Statements of Operations (Unaudited; In thousands, except share and per share amounts) | |||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| 2026 | 2025 | 2026 | 2025 | ||||||||||||
| Collaboration revenue | $ | 7,877 | $ | 2,954 | $ | 13,563 | $ | 3,374 | |||||||
| Operating expenses: | |||||||||||||||
| General and administrative | 46,565 | 3,679 | 50,717 | 7,852 | |||||||||||
| Research and development | 49,007 | 7,910 | 55,904 | 16,457 | |||||||||||
| Gain on lease termination | — | — | (10 | ) | — | ||||||||||
| Total operating expenses | 95,572 | 11,589 | 106,611 | 24,309 | |||||||||||
| Loss from operations | (87,695 | ) | (8,635 | ) | (93,048 | ) | (20,935 | ) | |||||||
| Other income (expense): | |||||||||||||||
| Interest income | 157 | 198 | 336 | 368 | |||||||||||
| Interest expense | (5 | ) | (45 | ) | (9 | ) | (172 | ) | |||||||
| Loss on issuance of liability-classified warrants and related issuance costs | (90,011 | ) | — | (90,011 | ) | — | |||||||||
| Changes in fair value of financial instruments | 24,487 | — | 24,487 | — | |||||||||||
| Total other income (expense), net | (65,372 | ) | 153 | (65,197 | ) | 196 | |||||||||
| Net loss | $ | (153,067 | ) | $ | (8,482 | ) | $ | (158,245 | ) | $ | (20,739 | ) | |||
| Net loss per common share – basic and diluted | $ | (24.14 | ) | $ | (2.67 | ) | $ | (28.39 | ) | $ | (7.33 | ) | |||
| Weighted average common shares outstanding – basic and diluted | 6,340,844 | 3,181,980 | 5,574,272 | 2,828,568 | |||||||||||
| Cue Biopharma, Inc. Condensed Consolidated Balance Sheets (Unaudited, In thousands) | |||||||
| June 30, 2026 | December 31, 2025 | ||||||
| Assets | |||||||
| Cash and cash equivalents | $ | 17,392 | $ | 27,136 | |||
| Other assets | 13,315 | 15,076 | |||||
| Total assets | $ | 30,707 | $ | 42,212 | |||
| Liabilities and stockholders’ equity | |||||||
| Liabilities | $ | 28,397 | $ | 15,780 | |||
| Stockholders' equity | 2,310 | 26,432 | |||||
| Total liabilities and stockholders’ equity | $ | 30,707 | $ | 42,212 | |||
About Cue Biopharma
Cue Biopharma (Nasdaq: CUE) is a clinical stage biopharmaceutical company focused on advancing a portfolio of potentially transformative therapies aimed at enabling functional cures across immunological disorders. Its lead asset, CUE-221, is a novel anti-IgE antibody with a dual mechanism of action, currently in Phase 2 development for allergic diseases. In addition, Cue developed the Immuno-STAT® platform which selectively targets disease-specific T cells in vivo without broad immune modulation. Its lead autoimmune candidate, CUE-401, is advancing towards Phase 1 and was designed to regulate inflammation and drive Treg-mediated tolerance. Cue is led by an experienced management team with deep expertise in identifying, acquiring, and advancing promising drug candidates.
Cautionary Note Regarding Forward-Looking Statements
This 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, the company’s belief regarding the potential benefits and applications of its drug candidates and programs, including the company’s plans to further advance its differentiating Immuno-STAT platform and its lead asset, CUE-221, and its lead autoimmune candidate, CUE-401, including expected timing of clinical trial initiation and data readout: the company’s expectations for its newly appointed executive officers and their contributions to the company; the expected benefits from the company’s license agreement with Ascendant; and expectations regarding the company’s growth, 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,” “promise,” “potential” 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 ability to maintain and establish collaboration, licensing and other arrangements; 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; the company’s ability to achieve profitability; potential setbacks in the company’s research and development efforts for its current and future drug product candidates, 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; potential challenges associated with clinical trials conducted in China and the company’s access to, and acceptability of, the data therefrom; its ability to secure required FDA or other governmental approvals for its product candidates and the breadth of any approved indication; 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 and Media Contact
Agnes Lee
Chief Investor Relations & Communications Officer
Marie Campinell
Senior Director, Corporate Communications
ir@cuebio.com
Cue Biopharma, Inc.
