Actinium Pharmaceuticals to Present ATNM-400 Program Update at SNMMI 2026 Conference on May 31-June 2 and Provides NYSE American Listing Standards Notice
Rhea-AI Summary
Actinium Pharmaceuticals (NYSE American: ATNM) will present new ATNM-400 Actinium-225 antibody radioconjugate data at the SNMMI 2026 meeting in Los Angeles through three scientific posters covering prostate cancer, non-small cell lung cancer and radioconjugate optimization.
The company also received an NYSE American notice for not meeting certain stockholders’ equity listing standards and must submit a compliance plan by June 26, 2026, to avoid potential delisting actions by November 27, 2027.
AI-generated analysis. Not financial advice.
Positive
- ATNM-400 featured in three SNMMI 2026 scientific presentations
- NYSE American notice has no immediate effect on ATNM share listing
- Company can submit compliance plan by June 26, 2026 to address standards
Negative
- Stockholders’ equity $2.3 million vs. $4.0 million minimum requirement
- Net losses reported in last five fiscal years through December 31, 2025
- Non-compliance with NYSE American Sections 1003(a)(ii) and (iii)
- Risk of NYSE American delisting if compliance not regained by November 27, 2027
Key Figures
Market Reality Check
Peers on Argus
ATNM gained 9.57% with mixed peer moves: one notable gainer (GNTA +4.78%) and several decliners (e.g., CUE -4.7%), pointing to a stock-specific reaction rather than a broad biotechnology move.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| May 06 | Conference abstracts | Positive | -1.6% | Announced three SNMMI 2026 abstracts highlighting ATNM-400 and radiochemistry work. |
| Apr 22 | Preclinical data update | Positive | -10.9% | Reported compelling pan-tumor ATNM-400 efficacy data at AACR 2026 across multiple cancers. |
| Apr 22 | Mechanism of action data | Positive | -10.9% | Detailed mutation-agnostic Actimab-A activity and combinations in AML models at AACR 2026. |
| Apr 06 | Upcoming AACR data | Positive | +11.2% | Previewed AACR abstracts with new ATNM-400 solid tumor data and Actimab-A mechanism work. |
| Feb 17 | Conference preview | Positive | -2.7% | Announced two planned AACR 2026 abstracts on ATNM-400 and Actimab-A theranostic platforms. |
Recent news has largely been positive on preclinical and pipeline progress, yet the stock more often traded lower on these updates, with only one notably positive price reaction.
Over the last few months, Actinium has repeatedly highlighted its Ac‑225 radioconjugate platforms, especially ATNM‑400 across multiple solid tumor models and Actimab‑A in AML. Several AACR and SNMMI‑related announcements emphasized pan‑tumor activity and differentiated mechanisms, yet four of five prior news events with similar scientific focus were followed by negative or modestly negative price moves. Today’s update combines another ATNM‑400 data showcase with a NYSE American listing compliance notice, adding a new regulatory overhang to an R&D‑driven story.
Market Pulse Summary
This announcement combines positive scientific momentum for ATNM‑400 with a material listing compliance risk. New SNMMI 2026 presentations reinforce mutation‑agnostic, pan‑tumor ambitions, while the NYSE American notice highlights stockholders’ equity of $2.3 million versus a required $4.0 million and a $33.9 million 2025 net loss. Investors may track the compliance plan due June 26, 2026, progress toward the November 27, 2027 deadline, cash levels, and how pipeline data evolve toward clinical milestones.
Key Terms
actinium-225 medical
antibody radioconjugate medical
non-small cell lung cancer medical
chelator-to-antibody ratio technical
pharmacokinetics medical
stockholders' equity financial
continued listing standards regulatory
delisting regulatory
AI-generated analysis. Not financial advice.
With the SNMMI 2026 program now finalized, the Company is providing updated presentation details, including poster titles, presenters, dates, and times. The data to be presented reinforce the meaningful progress of the ATNM-400 program and its potential as a mutation-agnostic, pan-tumor therapy, while also demonstrating the strength of the underlying radioconjugate platform that supports Actinium's broader pipeline. The Company anticipates multiple catalysts for ATNM-400, Actimab-A and Iomab-ACT in 2H:2026 that are expected to demonstrate the clinical potential of these programs.
ATNM-400 SNMMI 2026 Presentation Details
Poster Title: ATNM-400: A First-in-Class Non-PSMA Actinium-225 Antibody Radioconjugate Demonstrates Superior Efficacy to PSMA-617 Radioligands and ARPIs With Favorable Safety Profile in Prostate Cancer Models
Presenter: Sumit Mukherjee Ph.D., Actinium Pharmaceuticals, Inc.
Session: Oncology: Discovery & Translational Meet the Author Session
Date & Time: Tuesday, June 2, 2026 11:30am-12:15pm PT |
Poster Title: ATNM-400: A First-in-Class Actinium-225 Antibody Radioconjugate Demonstrating Durable, Mutation-Agnostic Anti-Tumor Activity in Non-Small Cell Lung Cancer Models
Presenter: Shiva Kazerounian Ph.D., Actinium Pharmaceuticals, Inc.
Session: Oncology: Discovery & Translational Meet the Author Session
Date & Time: Tuesday, June 2, 2026, 11:30am-12:15pm PT |
Poster Title: Optimizing Chelator-to-Antibody Ratio Improves Tumor Targeting and Pharmacokinetics of 225Ac-Labeled Antibodies
Presenter: Shiva Kazerounian Ph.D., Actinium Pharmaceuticals, Inc.
Session: MTA05 RPSC/CMIIT POPs and Science Pavilion Mixer
Date & Time: Sunday, May 31, 2026, 7:30-8:00pm PT |
The posters will be available on the Company website shortly after the presentations at https://ir.actiniumpharma.com/presentations-webinars.
NYSE American Continued Listing Standards Notice
Actinium also announced today that it has received a notice (the "Notice") from the NYSE American LLC ("NYSE American") indicating that the Company is not in compliance with the continued listing standards set forth in Section 1003(a)(ii) of the NYSE American Company Guide (the "Company Guide"), which requires a listed company to maintain stockholders' equity of
In connection with the non-compliance with Sections 1003(a)(ii) and (iii) of the Company Guide, the Company must submit a compliance plan by June 26, 2026, advising of actions the Company has taken or will take to regain compliance with the continued listing standards by November 27, 2027 (the "Plan Period Deadline"). If the NYSE American determines to accept the plan, the Company will be notified in writing and will be subject to periodic reviews, including quarterly monitoring, for compliance with the plan.
If the Company does not submit a plan or if the plan is not accepted, delisting proceedings will commence. Furthermore, if the plan is accepted but the Company is not in compliance with the continued listing standards by the Plan Period Deadline which is eighteen months from the receipt of the notice or November 27, 2027, or if the Company does not make progress consistent with the plan during the plan period, Exchange staff will initiate delisting proceedings as appropriate. The Company may appeal a staff delisting determination in accordance with Section 1010 and Part 12 of the Company Guide.
Actinium currently intends to submit a plan to regain compliance within the required timeframe. There can be no assurance that the Company will be able to achieve compliance with the NYSE American's continued listing standards within the required timeframe of eighteen months from date of receipt of the notice or November 27, 2027.
About Actinium Pharmaceuticals, Inc.
Actinium is a pioneer in targeted radiotherapies designed to improve outcomes for patients with cancer. The company employs a biology-driven approach to develop differentiated radiopharmaceuticals for solid tumors and hematologic malignancies. Its mission is to transform cancer treatment through innovative radioconjugates that maximize therapeutic efficacy while minimizing toxicity to healthy tissue by combining expertise in tumor biology, translational medicine, and radiochemistry. Since inception, Actinium has focused on developing innovative radiotherapies. Its pipeline reflects this strategy across three areas: (1) solid tumor therapeutics including ATNM-400 and Actimab-A with pan-tumor potential; (2) Actimab-A as a therapeutic backbone for acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) in collaboration with the National Cancer Institute (NCI); and (3) targeted conditioning agents including Iomab-B for bone marrow transplant and Iomab-ACT for cell and gene therapy conditioning. ATNM-400 targets a novel antigen distinct from PSMA and has demonstrated preclinical activity across metastatic castration-resistant prostate cancer (mCRPC), non-small cell lung cancer (NSCLC), and breast cancer. Actimab-A has shown improved survival in relapsed/refractory AML with CLAG-M and is advancing toward a Phase 2/3 trial, with additional development ongoing through a CRADA with the NCI. Actinium is also advancing preclinical solid tumor programs and holds ~250 patents and patent applications, including intellectual property related to cyclotron-based production of Ac-225. For more information, please visit www.actiniumpharma.com.
Forward-Looking Statements
This press release may contain projections or other "forward-looking statements" within the meaning of the "safe-harbor" provisions of the private securities litigation reform act of 1995 regarding future events or the future financial performance of the Company which the Company undertakes no obligation to update. These statements, including statements as related to regaining compliance with the rules of the NYSE American and submission of a compliance plan, are based on management's current expectations and are subject to risks and uncertainties that may cause actual results to differ materially from the anticipated or estimated future results, including the risks and uncertainties associated with preliminary study results varying from final results, estimates of potential markets for drugs under development, clinical trials, actions by the FDA and other governmental agencies, regulatory clearances, responses to regulatory matters, the market demand for and acceptance of Actinium's products and services, performance of clinical research organizations and other risks detailed from time to time in Actinium's filings with the Securities and Exchange Commission (the "SEC"), including without limitation its most recent annual report on form 10-K, subsequent quarterly reports on Forms 10-Q and Forms 8-K, each as amended and supplemented from time to time.
Investors: investorrelations@actiniumpharma.com
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SOURCE Actinium Pharmaceuticals, Inc.