IMUNON (NASDAQ: IMNN) posts Q1 2026 loss while IMNN-001 shows strong survival data
Rhea-AI Filing Summary
IMUNON, Inc. reported a first quarter 2026 net loss of $4.3 million, or $0.84 per share, compared with a net loss of $4.1 million, or $3.15 per share, a year earlier. Operating expenses rose slightly to $4.3 million, driven mainly by research and development spending of $2.3 million as the company advances its OVATION 3 Phase 3 trial in advanced ovarian cancer. General and administrative costs were stable at $2.0 million.
Net cash used in operations was $4.0 million, and cash and cash equivalents totaled $4.8 million as of March 31, 2026. IMUNON highlighted final Phase 2 OVATION 2 data showing a 14.7‑month median overall survival increase with IMNN‑001 versus standard chemotherapy, and a 24.2‑month median overall survival increase when combined with standard chemotherapy and PARP inhibitors. The FDA has reviewed and is aligned with the Phase 3 protocol for IMNN‑001, confirming a path to a future BLA filing.
Positive
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Negative
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Insights
IMUNON shows strong IMNN-001 data while quarterly loss and cash burn remain modest.
IMUNON reported a Q1 2026 net loss of $4.3M on operating expenses of $4.3M, reflecting ongoing investment in the pivotal Phase 3 OVATION 3 study. Research and development was $2.3M, slightly above the prior year, while general and administrative held at $2.0M.
Cash and cash equivalents were $4.8M as of March 31, 2026, with net cash used in operations of $4.0M in the quarter. This indicates a limited cash runway unless supplemented by future financing or partnerships, though exact duration is not stated in the text.
Strategically, the key development is the final Phase 2 OVATION 2 data showing a median overall survival benefit of 14.7 months versus standard chemotherapy and 24.2 months when combined with PARP inhibitors. The FDA’s alignment with the Phase 3 protocol and confirmation of a path to a BLA filing underscores regulatory clarity around IMNN‑001’s late-stage development. Subsequent filings may provide more detail on enrollment progress and funding plans for OVATION 3.
8-K Event Classification
Key Figures
Key Terms
overall survival medical
Phase 3 OVATION 3 Study medical
Biologics License Application regulatory
strategic reorganization financial
non-viral DNA technology technical
Earnings Snapshot
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Item 2.02 Results of Operations and Financial Condition.
On May 12, 2026, Imunon, Inc. issued a press release reporting its financial results for the quarter ended March 31, 2026. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
On May 5, 2026, Imunon, Inc. announced it would hold a conference call on May 12, 2026 to discuss its financial results for the quarter ended March 31, 2026 and provide a business update. The conference call will also be broadcast live on the internet at https://edge.media-server.com/mmc/p/9n9b48gb/.
The information in this report, including the exhibit hereto, 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 or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. Such information shall not be incorporated by reference into any filing with the Securities and Exchange Commission made by Imunon, Inc., whether made before or after the date hereof, regardless of any general incorporation language in such filing.
The press release contains forward-looking statements which involve certain risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Please refer to the cautionary note in the press release regarding these forward-looking statements.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No. |
Description | |
| 99.1 | Press Release dated May 12, 2026 | |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document) |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| IMUNON INC. | ||
| Dated: May 12, 2026 | By: | /s/ Jeffrey Church |
| Jeffrey Church | ||
| Chief Financial Officer | ||
Exhibit 99.1
IMUNON Reports First Quarter 2026 Financial Results
and Provides Business Update
IMNN-001 is the First and Only frontline treatment candidate to demonstrate the potential for a clinically meaningful overall survival benefit in women newly diagnosed with ovarian cancer
Enrollment in the Phase 3 OVATION 3 Study of IMNN-001 is expected to be completed by Q1 2029, supported by remarkable Phase 2 data showing significant overall survival improvement
FDA has reviewed and is aligned with Phase 3 protocol, confirms path to BLA Filing
Company to hold conference call today at 11:00 a.m. ET
LAWRENCEVILLE, N.J., May 12, 2026 – IMUNON, Inc. (NASDAQ: IMNN), a clinical-stage company in late-stage development with its DNA-mediated immunotherapy, today reported financial results for the three months ended March 31, 2026, and highlighted recent business updates including progress in advancing Phase 3 clinical development of its lead candidate IMNN-001 in newly diagnosed advanced ovarian cancer.
“Enrollment in our pivotal Phase 3 OVATION 3 trial continues ahead of plan, reflecting patient interest and strong conviction among principal investigators and the broader medical community in IMNN-001’s therapeutic potential,” said Stacy Lindborg, Ph.D., President and Chief Executive Officer of IMUNON. “Coupled with the unprecedented overall survival benefit observed in our Phase 2 (OVATION 2) study and an aligned path to BLA filing, IMNN-001 is well positioned to potentially transform the standard of care in advanced ovarian cancer.”
RECENT DEVELOPMENTS
Final Phase 2 OVATION 2 Study Data Show Continued Overall Survival Improvement with IMNN-001 in Women with Newly Diagnosed Advanced Ovarian Cancer – On March 25, 2026, the Company announced final data from the completed Phase 2 OVATION 2 clinical trial evaluating IMNN-001 in combination with standard of care (SoC) neoadjuvant and adjuvant chemotherapy (N/ACT) in 112 women with newly diagnosed advanced ovarian cancer. IMUNON previously reported a median 11.1-month increase in overall survival (40.5 vs. 29.4 months) in the IMNN-001 treatment arm compared to SoC chemotherapy alone. Following the most recent and final data assessment, the Company reported a median 14.7-month increase in overall survival (45.1 vs. 30.4 months) in women in the IMNN-001 treatment arm compared to SoC alone, demonstrating continuous improvement in overall survival (3.6 months delta). In addition, the new IMNN-001 data showed that women treated with IMNN-001 and SoC chemotherapy plus poly ADP-ribose polymerase (PARP) inhibitors as part of maintenance therapy achieved a median increase in overall survival of 24.2 months (65.6 vs. 41.4 months) compared to SoC chemotherapy alone. Importantly, with these new efficacy results, IMNN-001 continues to show a highly favorable safety and tolerability profile across all clinical trials, further reinforcing the potential of this IL-12 immunotherapy to represent a landmark advance in treatment of this disease.
IMUNON Sharpens Focus on its Promising Pivotal Phase 3 Ovarian Cancer Study – On February 5, 2026, the Company announced a strategic reorganization, the goal of which was to reduce operating expenses while supporting the Company’s focused strategy to rapidly advance the pivotal Phase 3 OVATION 3 clinical trial.
FIRST QUARTER 2026 FINANCIAL RESULTS
Net loss for the first quarter of 2026 was $4.3 million, or $0.84 per share, compared with a net loss of $4.1 million, or $3.15 per share, for the first quarter of 2025. Operating expenses were $4.3 million for the first quarter of 2026, compared to $4.1 million for the first quarter of 2025.
Research and development expenses increased to $2.3 million in the first quarter of 2026 from $2.2 million in the same period of 2025. During 2025, the Company initiated enrollment in the OVATION 3 Study and in 2026 closed out the OVATION 2 Study.
General and administrative expenses remained unchanged at $2.0 million in each of the first quarters of 2026 and 2025.
Net cash used for operating activities was $4.0 million for the first quarter of 2026, compared with $2.8 million for the same period last year. This increase was primarily due to trial-related expenses associated with the OVATION 3 trial.
As of March 31, 2026, cash and cash equivalents were $4.8 million.
Conference Call and Webcast
The Company will be hosting a conference call to review first quarter 2026 financial results and provide a business update today, May 12, 2026, at 11:00 a.m. EDT. To participate in the call, please dial 800-715-9871 (U.S. and Canada/Toll Free) or 646-307-1963 (U.S./Toll) and ask for the IMUNON First Quarter 2026 Financial Results Call (Conference ID 8083343). A live webcast of the call will also be available here.
An audio replay of the call will be available for 90 days and can be accessed at 800-770-2030 (U.S. and Canada/Toll Free), 609-800-9909 (U.S./Toll) or 647-362-9199 (Canada/Toll) using replay access code 8083343#.
About IMUNON
IMUNON is a clinical-stage biotechnology company focused on advancing a portfolio of innovative treatments that harness the body’s natural mechanisms to generate safe, effective and durable responses across a broad array of human diseases, constituting a differentiating approach from conventional therapies. IMUNON is developing its non-viral DNA technology across its modalities. The first modality, TheraPlas®, is developed for the gene-based delivery of cytokines and other therapeutic proteins in the treatment of solid tumors where an immunological approach is deemed promising. The second modality, PlaCCine®, is developed for the gene delivery of viral antigens that can elicit a strong immunological response.
The Company’s lead clinical program, IMNN-001, is a DNA-based immunotherapy for the localized treatment of advanced ovarian cancer that has completed multiple clinical trials including one Phase 2 clinical trial (OVATION 2) and is currently conducting a Phase 3 clinical trial (OVATION 3). The first patient was dosed in the Company’s Phase 3 pivotal study in the third quarter of 2025. IMNN-001 works by instructing the body to produce safe and durable levels of powerful cancer-fighting molecules, such as interleukin-12 and interferon gamma, at the tumor site. Additionally, the Company has completed dosing in a first-in-human study of its COVID-19 booster vaccine (IMNN-101). The Company will continue to leverage these modalities and to advance, either directly or through partnership, the technological frontier of plasmid DNA to better serve patients with difficult-to-treat conditions. For more information, please visit www.imunon.com.
Forward-Looking Statements
IMUNON wishes to inform readers that forward-looking statements in this news release are made pursuant to the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including, but not limited to, statements regarding the expected reduction of operating expenses related to the strategic reorganization, the timing of enrollment of the Company’s clinical trials, the potential of any therapies developed by the Company to fulfill unmet medical needs, the market potential for the Company’s products, if approved, the potential efficacy and safety profile of our product candidates, and the Company’s plans and expectations with respect to its development programs more generally, are forward-looking statements. We generally identify forward-looking statements by using words such as “may,” “will,” “expect,” “plan,” “anticipate,” “estimate,” “intend” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances), and include statements regarding our planned stock split. Readers are cautioned that such forward-looking statements involve risks and uncertainties including, without limitation, risks and uncertainties related to unforeseen changes in the course of research and development activities and in clinical trials, including the fact that interim results are not necessarily indicative of final results; the uncertainties of and difficulties in analyzing interim clinical data; the significant expense, time and risk of failure in conducting clinical trials; the need for IMUNON to evaluate its future development plans; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in IMUNON’s filings with the Securities and Exchange Commission. IMUNON assumes no obligation, except to the extent required by law, to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise.
Contacts:
Media |
Investors | |
| CG Life | ICR Healthcare | |
| Jenna Urban | Peter Vozzo | |
| 212-253-8881 | 443-213-0505 | |
| jurban@cglife.com | peter.vozzo@icrhealthcare.com |
(Tables to Follow)
IMUNON, Inc.
Condensed Consolidated Statements of Operations
(in thousands except per share amounts)
| Three Months Ended March 31, | ||||||||
| 2026 | 2025 | |||||||
| Operating expenses: | ||||||||
| Research and development | $ | 2,337 | $ | 2,165 | ||||
| General and administrative | 1,970 | 1,980 | ||||||
| Total operating expenses | 4,307 | 4,145 | ||||||
| Loss from operations | (4,307 | ) | (4,145 | ) | ||||
| Other income (expense): | ||||||||
| Investment and other income | 58 | 43 | ||||||
| Net loss | $ | (4,249 | ) | $ | (4,102 | ) | ||
| Net loss per common share | ||||||||
| Basic and diluted | $ | (0.84 | ) | $ | (3.15 | ) | ||
| Weighted average shares outstanding | ||||||||
| Basic and diluted | 5,029 | 1.301 | ||||||
IMUNON, Inc.
Selected Balance Sheet Information
(in thousands)
| March 31, 2026 | December 31, 2025 | |||||||
| ASSETS | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 4,794 | $ | 8,781 | ||||
| Advances, deposits on clinical programs and other current assets | 1,827 | 1,943 | ||||||
| Total current assets | 6,621 | 10,724 | ||||||
| Property and equipment | 460 | 530 | ||||||
| Other assets | ||||||||
| Operating lease right-of-use assets | 888 | 984 | ||||||
| Deposits and other assets | 50 | 50 | ||||||
| Total other assets | 938 | 1,034 | ||||||
| Total assets | $ | 8,019 | $ | 12,288 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities | ||||||||
| Accounts payable and accrued liabilities | $ | 3,747 | $ | 4,218 | ||||
| Operating lease liability – current portion | 419 | 406 | ||||||
| Total current liabilities | 4,166 | 4,624 | ||||||
| Operating lease liability – noncurrent portion | 493 | 602 | ||||||
| Total liabilities | 4,659 | 5,226 | ||||||
| Stockholders’ equity | ||||||||
| Common stock | 39 | 34 | ||||||
| Additional paid-in capital | 428,953 | 428,411 | ||||||
| Accumulated deficit | (425,547 | ) | (421,298 | ) | ||||
| 3,445 | 7,147 | |||||||
| Less: Treasury stock | (85 | ) | (85 | ) | ||||
| Total stockholders’ equity | 3,360 | 7,062 | ||||||
| Total liabilities and stockholders’ equity | $ | 8,019 | $ | 12,288 | ||||
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