IMUNON to Hold Second Quarter 2026 Financial Results and Business Update Conference Call on Tuesday, August 11, 2026
IMUNON (Nasdaq: IMNN) will hold a conference call at 11:00 a.m. EDT on Tuesday, August 11, 2026 to discuss its second quarter 2026 financial results and provide a business update.
Rhea-AI Summary
IMUNON (Nasdaq: IMNN) will hold a conference call at 11:00 a.m. EDT on Tuesday, August 11, 2026 to discuss its second quarter 2026 financial results and provide a business update.
Management will also review progress in advancing Phase 3 clinical development of lead DNA-based IL-12 immunotherapy IMNN-001 for newly diagnosed advanced ovarian cancer, part of IMUNON’s non-viral DNA-based gene therapy portfolio. Investors can join via phone using Conference ID 8021948 or by live webcast, with a 90-day audio replay available by phone with replay code 8021948#.
Positive
- None.
Negative
- None.
Details
Market reaction after 2Q26 earnings report: IMNN +5.70% in the Aug 4 session
In the Aug 4 session, IMNN gained 5.70%, reflecting a notable positive market reaction. Argus tracked a peak move of +3.6% during that session. Argus tracked a trough of -5.5% from its starting point during tracking. Our momentum scanner triggered 7 alerts that day, indicating moderate trading interest and price volatility.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
- Reporting Period
- Second quarter 2026
- Financial results
- Quarter End
- June 30, 2026
- Second-quarter reporting period
- Conference Call Date
- August 11, 2026
- Financial results and business update call
- Conference Call Time
- 11:00 a.m. EDT
- August 11, 2026
- Development Stage
- Phase 3
- IMNN-001 in advanced ovarian cancer
- Audio Replay
- 90 days
- Availability following the conference call
Previous Conferences,earnings date Reports
-
Scheduled first-quarter results and a Phase 3 clinical development update.
-
Scheduled annual results and a Phase 3 clinical development update.
-
Scheduled third-quarter results and a Phase 3 clinical development update.
-
Scheduled second-quarter results and a Phase 3 clinical trial update.
-
Scheduled first-quarter results and clinical program updates before Phase 3 initiation.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
dna-mediated immunotherapies medical
interleukin-12 medical
phase 3 clinical trial medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
LAWRENCEVILLE, N.J., Aug. 04, 2026 (GLOBE NEWSWIRE) -- IMUNON, Inc. (Nasdaq: IMNN), a clinical-stage biotechnology company developing DNA-mediated immunotherapies, today announced that the Company will host a conference call at 11:00 a.m. EDT on Tuesday, August 11, 2026 to discuss financial results for the second quarter ended June 30, 2026 and provide an update on its clinical development program with IMNN-001, a DNA-based interleukin-12 (IL-12) immunotherapy, including progress in advancing Phase 3 clinical development of its lead candidate IMNN-001 in newly diagnosed advanced ovarian cancer.
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 Second Quarter 2026 Financial Results Call (Conference ID 8021948). 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) or (609) 800-9909 (U.S./Toll) using replay access code 8021948#.
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-based gene therapy 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 Company’s lead clinical program, IMNN-001, is a DNA-based immunotherapy being developed for the localized treatment of advanced ovarian cancer. IMNN-001 has been evaluated in multiple clinical trials including one Phase 2 clinical trial (OVATION 2) and is currently being studied in the ongoing Phase 3 clinical trial (OVATION 3). 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 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 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 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.
Investor Contact:
Valter Pinto
KCSA Strategic Communications
212-896-1254
imunon@kcsa.com
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.