Full Press Release Details
Reports First Quarter 2026 Financial Results
Provides Business Update
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
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
has reviewed and is aligned with Phase 3 protocol, confirms path to BLA Filing
to hold conference call today at 11:00 a.m. ET
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.
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."
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.
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.
QUARTER 2026 FINANCIAL RESULTS
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
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.
and administrative expenses remained unchanged at $2.0 million in each of the first quarters of 2026 and 2025.
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.
of March 31, 2026, cash and cash equivalents were $4.8 million.
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
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#.
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.
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.
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.
| Media | Investors | |
| CG Life | ICR Healthcare | |
| Jenna Urban | Peter Vozzo | |
| 212-253-8881 | 443-213-0505 | |
| jurban@cglife.com | peter.vozzo@icrhealthcare.com |
Consolidated Statements of Operations
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 |
Balance Sheet Information
| 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 |