IMUNON Reports Third Quarter 2024 Financial Results and Provides Business Updates
IMUNON reported Q3 2024 financial results and provided updates on its clinical developments. The company highlighted compelling topline results from the OVATION 2 Study with IMNN-001 in advanced ovarian cancer, showing an 11.1-month overall survival improvement compared to standard care. The company plans to begin a 500-patient pivotal Phase 3 study in Q1 2025. Financial results showed $10.3 million in cash and investments as of September 30, 2024, with Q3 net loss of $4.9 million ($0.34 per share). Research and development expenses increased to $3.3 million from $2.0 million in Q3 2023.
IMUNON ha riportato i risultati finanziari del terzo trimestre 2024 e fornito aggiornamenti sui suoi sviluppi clinici. L'azienda ha evidenziato risultati promettenti dallo studio OVATION 2 con IMNN-001 nel cancro ovarico avanzato, mostrando un miglioramento della sopravvivenza globale di 11,1 mesi rispetto al trattamento standard. L'azienda prevede di iniziare uno studio pivotale di Fase 3 su 500 pazienti nel primo trimestre del 2025. I risultati finanziari hanno mostrato 10,3 milioni di dollari in contante e investimenti al 30 settembre 2024, con una perdita netta di 4,9 milioni di dollari (0,34 dollari per azione) nel terzo trimestre. Le spese per ricerca e sviluppo sono aumentate a 3,3 milioni di dollari rispetto ai 2,0 milioni del terzo trimestre 2023.
IMUNON informó los resultados financieros del tercer trimestre de 2024 y proporcionó actualizaciones sobre sus desarrollos clínicos. La empresa destacó resultados atractivos del Estudio OVATION 2 con IMNN-001 en cáncer de ovario avanzado, mostrando una mejora de 11.1 meses en la supervivencia general en comparación con el tratamiento estándar. La empresa planea comenzar un estudio pivotal de fase 3 con 500 pacientes en el primer trimestre de 2025. Los resultados financieros mostraron 10.3 millones de dólares en efectivo e inversiones al 30 de septiembre de 2024, con una pérdida neta de 4.9 millones de dólares (0.34 dólares por acción) en el tercer trimestre. Los gastos de investigación y desarrollo aumentaron a 3.3 millones de dólares desde 2.0 millones en el tercer trimestre de 2023.
IMUNON은 2024년 3분기 재무 결과를 발표하고 임상 개발에 대한 업데이트를 제공했습니다. 이 회사는 고급 난소암에 대한 IMNN-001을 포함한 OVATION 2 연구에서 매력적인 주요 결과를 강조하며, 표준 치료에 비해 전체 생존 기간이 11.1개월 개선되었음을 보여주었습니다. 회사는 2025년 1분기에 500명 환자를 대상으로 하는 중요한 3상 연구를 시작할 계획입니다. 2024년 9월 30일 기준으로 재무 결과는 현금 및 투자로 1,030만 달러를 보여주었으며, 3분기 순손실은 490만 달러(주당 0.34달러)였습니다. 연구 및 개발 비용은 2023년 3분기의 200만 달러에서 330만 달러로 증가했습니다.
IMUNON a annoncé les résultats financiers du troisième trimestre 2024 et fourni des mises à jour sur ses développements cliniques. L'entreprise a mis en avant des résultats encourageants de l'étude OVATION 2 avec IMNN-001 dans le cancer des ovaires avancé, montrant une amélioration de 11,1 mois de la survie globale par rapport aux soins standards. L'entreprise prévoit de commencer une étude pivot de Phase 3 sur 500 patients au premier trimestre 2025. Les résultats financiers ont montré 10,3 millions de dollars en liquidités et investissements au 30 septembre 2024, avec une perte nette de 4,9 millions de dollars (0,34 dollar par action) pour le troisième trimestre. Les dépenses de recherche et développement ont augmenté à 3,3 millions de dollars contre 2,0 millions de dollars au troisième trimestre 2023.
IMUNON hat die finanziellen Ergebnisse für das dritte Quartal 2024 veröffentlicht und Updates zu seinen klinischen Entwicklungen bereitgestellt. Das Unternehmen hob überzeugende Ergebnisse aus der OVATION 2-Studie mit IMNN-001 bei fortgeschrittenem Ovarialkarzinom hervor, die eine Verbesserung der Gesamtüberlebensrate um 11,1 Monate im Vergleich zur Standardbehandlung zeigten. Das Unternehmen plant, im ersten Quartal 2025 eine entscheidende Phase-3-Studie mit 500 Patienten zu beginnen. Die finanziellen Ergebnisse zeigten zum 30. September 2024 10,3 Millionen Dollar an Bargeld und Investitionen, mit einem Nettoverlust von 4,9 Millionen Dollar (0,34 Dollar pro Aktie) im dritten Quartal. Die Forschungs- und Entwicklungskosten stiegen von 2,0 Millionen Dollar im dritten Quartal 2023 auf 3,3 Millionen Dollar.
- OVATION 2 Study showed 11.1-month increase in median overall survival for IMNN-001
- Patients receiving PARP inhibitors showed stronger results with hazard ratio of 0.41
- Secured $10 million in gross proceeds through registered direct financing
- Three-month improvement in progression-free survival compared to standard care
- Net loss increased to $4.9 million in Q3 2024 from $3.5 million in Q3 2023
- R&D expenses increased 65% to $3.3 million compared to Q3 2023
- Current cash position only sufficient until Q3 2025
Insights
The Q3 2024 results reveal significant developments for IMUNON, particularly in their advanced ovarian cancer program. The standout metrics include an 11.1-month improvement in overall survival with IMNN-001 compared to standard care and even more impressive results in PARP inhibitor-treated patients. The company's financial position shows
The quarterly financials show increased R&D expenses at
Conference call today at 11:00 a.m. ET
LAWRENCEVILLE, N.J., Nov. 07, 2024 (GLOBE NEWSWIRE) -- IMUNON, Inc. (NASDAQ: IMNN), a clinical-stage company in late-stage development with its DNA-mediated immunotherapy, today reported financial results for the three and nine months ended September 30, 2024. The Company also provided an update on its clinical development of IMNN-001 including progress toward commencing a Phase 3 study in advanced ovarian cancer, and an update on IMNN-101, its seasonal COVID-19 booster candidate.
“The third quarter was a period of important milestones and outstanding progress for IMUNON, driven largely by presentation of highly compelling topline results from our OVATION 2 Study with IMNN-001 in advanced ovarian cancer,” said Stacy Lindborg, Ph.D., president and chief executive officer of IMUNON. “In this study, treatment with IMNN-001 was associated with an overall survival improvement of 11.1 months compared to treatment with standard of care, and results were even stronger in the subset of patients who were also treated with PARP inhibitors. Building on this momentum, we have been highly encouraged by the interest in these results among global leaders from the medical and scientific communities. We have also engaged with the U.S. Food and Drug Administration to craft the design of our planned registrational study and are preparing for an in-person End-of-Phase 2 meeting with the agency later this month. We remain on track to begin our planned 500-patient pivotal Phase 3 study during the first quarter of 2025.”
“Tomorrow afternoon we will be presenting new OVATION 2 data at the Society for Immunotherapy of Cancer 39th Annual Meeting. Our abstract is being highlighted as a late-breaking acceptance, so compelling that it was accepted after the deadline. Given the strength of the data, we are unsurprised with SITC’s decision to include our data for presentation. This is an exceptional opportunity to gain further awareness for IMNN-001 and our trial results.”
“In summary, IMUNON is extraordinarily well-positioned to address the unmet need in a deadly cancer while also playing an important role in public health. We are justifiably excited about our prospects for patients and shareholders alike,” Dr. Lindborg concluded.
RECENT DEVELOPMENTS
IMNN-001 Immunotherapy
Presenting Additional Phase 2 data for IMNN-001 at SITC – On October 30, 2024 the Company announced the acceptance of a late-breaking presentation featuring new clinical data from the Phase 2 OVATION 2 Study of IMNN-001 at the Society for Immunotherapy of Cancer (SITC) 39th Annual Meeting, being held in Houston, TX. The presentation, titled “Phase I/II study of Safety and Efficacy of Intraperitoneal IMNN-001 with Neoadjuvant Chemotherapy of Paclitaxel and Carboplatin in Patients Newly Diagnosed with Advanced Epithelial Ovarian Cancer,” will be made on Friday, November 8, 2024 from 12:15-1:45 p.m. and 5:30-7:30 p.m. CST by Jennifer Scalici, M.D., Professor, Division of Gynecological Oncology, Emory University School of Medicine and a principal investigator in the trial.
Imunon Ovarian Cancer R&D Day – On September 18, 2024 the company held an Ovarian Cancer R&D Day in New York City that included presentations from executive management and a panel of renowned leaders in research and patient care including:
- Sid Kerkar, M.D., T cell biology review editor, Frontiers in Immunology. Dr. Kerkar discussed the important role of interleukin-12 (IL-12) in treating cancer.
- William Bradley, M.D., Professor, Obstetrics and Gynecology, Gynecologic Oncology, Medical College of Wisconsin. Dr. Bradley discussed the safety and efficacy of IMNN-001.
- L.J. Wei, Ph.D., Professor of Biostatistics, Harvard T.H. Chan School of Public Health. Dr. Wei discussed the opportunity to combine progression-free survival (PFS) and overall survival (OS) to provide a clinically interpretable evaluation of the IMNN-001 treatment effect.
- Amir Jazaeri, M.D., Vice Chair for Clinical Research, Director, Gynecologic Cancer Immunotherapy Program, Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center. Dr. Jazaeri discussed the ongoing Phase 1/2 study of IMNN-001 in combination with bevacizumab in advanced ovarian cancer, for which he serves as principal investigator, including the importance of minimal residual disease and early translational insights.
- Premal Thaker, M.D., Interim Chief of Gynecologic Oncology, David & Lynn Mutch Distinguished Professor of Obstetrics & Gynecology, Director of Gynecologic Oncology Clinical Research, Washington University School of Medicine, and the OVATION 2 Study Chair. Dr. Thaker discussed the OVATION 2 topline results and their clinical significance.
Positive topline results from the OVATION 2 Study in advanced ovarian cancer – On July 30, 2024, the Company announced topline results from the study that provide strong further validation of the potential safety and efficacy of IMNN-001 in the treatment of advanced ovarian cancer. Highlights from patients treated with IMNN-001 plus standard of care in a first-line treatment setting included:
- An 11.1 month increase in median OS compared with standard of care alone in the intent-to-treat (ITT) population.
- A hazard ratio in the ITT population of 0.74, which represents a
35% improvement in survival. - Among the approximately
90% of trial participants who received at least20% of specified treatments per-protocol in both study arms, patients in the IMNN-001 arm had a 15.7 month increase in median OS, representing a further extension of life with a hazard ratio of 0.64, a56% improvement in survival. - For the nearly
40% of trial participants treated with a poly ADP-ribose polymerase (PARP) inhibitor, the hazard ratio decreased further to 0.41, with median OS in the IMNN-001 treatment arm not yet reached at the time of database lock, compared with median OS of 37.1 months in the standard-of-care treatment arm.
The PFS results, the trial’s primary endpoint, support the OS results with:
- A three-month improvement in PFS compared with standard of care alone.
- A hazard ratio in the ITT population of 0.79, indicating a
27% improvement in delaying progression for the IMNN-001 treatment arm.
CORPORATE DEVELOPMENTS
Raised gross proceeds of
Additions to leadership team to ensure operational excellence and support future plans – On October 7, 2024, Susan Eylward was named General Counsel and Corporate Secretary. She was most recently Senior Counsel at Science 37, Inc., a solutions organization focused on decentralized clinical trials, where she was responsible for a variety of complex legal matters, including corporate governance, securities compliance, executive compensation and acquisitions.
Kristin Longobardi was named Senior Vice President of Operations, bringing more than two decades of experience in enhancing business processes and operations across the biotech and pharmaceutical sectors. Previously, she served as Vice President of R&D Quality, Operations and Performance at Biogen. Her expertise in portfolio management, financial planning and operational excellence will be pivotal in driving IMUNON’s operational frameworks toward supporting ambitious company growth.
THIRD QUARTER FINANCIAL RESULTS
The Company had
Research and development expenses were
Net loss was
YEAR-TO-DATE FINANCIAL RESULTS
Research and development expenses were
Year-to-date net loss was
Conference Call and Webcast
The Company is hosting a conference call at 11:00 a.m. ET today to provide a business update, discuss third quarter 2024 financial results and answer questions. To participate in the call, please dial 833-816-1132 (Toll-Free/North America) or 412-317-0711 (International/Toll) and ask for the IMUNON third quarter 2024 earnings call. A live webcast of the call will be available here.
The call will be archived for replay until November 21, 2024. The replay can be accessed at 877-344-7529 (U.S. Toll-Free), 855-669-9658 (Canada Toll-Free) or 412-317-0088 (International Toll), using the replay access code 10193110. A webcast of the call will be available here for 90 days.
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 Phase 2 development. 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 entered a first-in-human study of its COVID-19 booster vaccine (IMNN-101). IMUNON will continue to leverage these modalities and to advance the technological frontier of plasmid DNA to better serve patients with difficult-to-treat conditions, and to further strengthen IMUNON’s balance sheet through attractive business development opportunities. 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 timing for commencement of a Phase 3 trial of IMNN-001, the timing and outcome of the Company’s End-of-Phase 2 meeting with the FDA, the timing and 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). Readers are cautioned that such forward-looking statements involve risks and uncertainties including, without limitation, uncertainties relating 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 of 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@westwicke.com |
(Tables to Follow)
| IMUNON, Inc. | ||||||||||||||||
| Condensed Statements of Operations | ||||||||||||||||
| (in thousands except per share amounts) | ||||||||||||||||
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||||
| 2024 | 2023 | 2024 | 2023 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | $ | 3,293 | $ | 1,981 | $ | 9,407 | $ | 7,735 | ||||||||
| General and administrative | 1,668 | 1,923 | 5,579 | 7,328 | ||||||||||||
| Total operating expenses | 4,961 | 3,904 | 14,986 | 15,063 | ||||||||||||
| Loss from operations | (4,961 | ) | (3,904 | ) | (14,986 | ) | (15,063 | ) | ||||||||
| Other income (expense): | ||||||||||||||||
| Investment income | 116 | 427 | 423 | 962 | ||||||||||||
| Interest expense | - | - | - | (197 | ) | |||||||||||
| Loss on debt extinguishment | - | - | - | (329 | ) | |||||||||||
| Total other (expense) income, net | 116 | 427 | 423 | 436 | ||||||||||||
| Net loss | $ | (4,845 | ) | $ | (3,477 | ) | $ | (14,563 | ) | $ | (14,627 | ) | ||||
| Net loss per common share | ||||||||||||||||
| Basic and diluted | $ | (0.34 | ) | $ | (0.37 | ) | $ | (1.39 | ) | $ | (1.64 | ) | ||||
| Weighted average shares outstanding | ||||||||||||||||
| Basic and diluted | 14,445 | 9,377 | 10,503 | 8,926 | ||||||||||||
| IMUNON, Inc. | ||||||||
| Selected Balance Sheet Information | ||||||||
| (in thousands) | ||||||||
| ASSETS | September 30, 2024 | December 31, 2023 | ||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 10,312 | $ | 5,839 | ||||
| Investment securities and interest receivable | - | 9,857 | ||||||
| Advances, deposits and other current assets | 2,220 | 2,545 | ||||||
| Total current assets | 12,532 | 18,241 | ||||||
| Property and equipment | 564 | 752 | ||||||
| Other assets | ||||||||
| Deferred tax asset | - | 1,280 | ||||||
| Operating lease right-of-use assets, net | 1,245 | 1,595 | ||||||
| Deposits and other assets | 50 | 50 | ||||||
| Total other assets | 1,295 | 2,925 | ||||||
| Total assets | $ | 14,391 | $ | 21,918 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| Current liabilities | ||||||||
| Accounts payable – trade accrued liabilities | $ | 2,360 | $ | 3,515 | ||||
| Other accrued liabilities | 2,573 | 3,391 | ||||||
| Operating lease liabilities – current portion | 509 | 485 | ||||||
| Total current liabilities | 5,442 | 7,391 | ||||||
| Operating lease liabilities – non-current portion | 758 | 1,139 | ||||||
| Total liabilities | 6,200 | 8,530 | ||||||
| Stockholders' equity | ||||||||
| Common stock | 145 | 94 | ||||||
| Additional paid-in capital | 410,877 | 401,501 | ||||||
| Accumulated other comprehensive gain (loss) | - | 61 | ||||||
| Accumulated deficit | (402,746 | ) | (388,183 | ) | ||||
| 8,276 | 13,473 | |||||||
| Less: Treasury stock | (85 | ) | (85 | ) | ||||
| Total stockholders' equity | 8,191 | 13,388 | ||||||
| Total liabilities and stockholders' equity | $ | 14,391 | $ | 21,918 | ||||
# # #
FAQ
What were IMUNON's (IMNN) key financial results for Q3 2024?
What were the main results from IMUNON's (IMNN) OVATION 2 Study?
When will IMUNON (IMNN) begin its Phase 3 study for ovarian cancer?
