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Actinium Pharmaceuticals Presents New Radiochemistry Data at SNMMI 2026 Demonstrating That CAR Optimization Improves Tumor Targeting and Pharmacokinetics of Actinium-225 Radioconjugates

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Actinium Pharmaceuticals (NYSE American: ATNM) presented new radiochemistry data at SNMMI 2026 on May 31, 2026, showing that optimizing chelator-to-antibody ratio (CAR) for Actinium-225 radioconjugates affects radiolabeling, antigen binding, internalization, and biodistribution.

Lower-CAR constructs maintained tumor uptake while reducing liver and spleen exposure, potentially widening the therapeutic index across Actinium’s radioconjugate pipeline.

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News Market Reaction – ATNM

-6.35%
2 alerts
-6.35% Session close to close
-3.4% Trough Tracked
$39.53M Market Cap
0.0x Rel. Volume

In the Jun 1 session, ATNM declined 6.35%, reflecting a notable negative market reaction. Argus tracked a trough of -3.4% from its starting point during tracking. Our momentum scanner triggered 2 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved -6.3% in the session following this news. A negative reaction despite technically po...
Analysis

The stock moved -6.3% in the session following this news. A negative reaction despite technically positive radiochemistry data would fit a recent pattern in which ATNM traded lower after upbeat preclinical and conference updates, such as moves of -10.86% on Apr 22, 2026. With shares already below the 200-day MA and 35.23% under the 52-week high, risk perception and balance sheet concerns from recent regulatory filings could overshadow platform advances and contribute to selling pressure.

Key Figures

CAR range tested: 0.7–9 Minimum effective CAR: CAR ≥1.7 Antigen binding low CAR: 91–98% +5 more
8 metrics
CAR range tested 0.7–9 Antibody-DOTA conjugate chelator-to-antibody ratios
Minimum effective CAR CAR ≥1.7 Enabled robust 225Ac labeling vs. CAR 0.7 insufficient
Antigen binding low CAR 91–98% Binding retention at CAR 0.7–3.2
Antigen binding high CAR 79–85% Binding retention at CAR 7–9
Tumor uptake duration 192 h Sustained tumor retention for both conjugates in vivo
Radiochemical purity >97% Stability of both conjugates over 7 days
Stability period 7 days Timeframe over which radiochemical purity remained above 97%
Low-CAR example CAR 2.5 Conjugate with reduced liver and spleen uptake in vivo

Historical Context

5 past events · Latest: May 06 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 06 Conference data update Positive -1.6% Three SNMMI 2026 abstracts on ATNM-400 and radioconjugate optimization.
Apr 22 Preclinical efficacy data Positive -10.9% Compelling pan-tumor ATNM-400 data across multiple solid tumor models.
Apr 22 Mechanism-of-action data Positive -10.9% Actimab-A mutation-agnostic activity and enhanced killing in AML combinations.
Apr 06 Conference preview Positive +11.2% Announcement of AACR 2026 abstracts for ATNM-400 and Actimab-A programs.
Feb 17 Conference scheduling Positive -2.7% Notice of two AACR 2026 abstracts focused on ATNM-400 and Actimab-A.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent preclinical and conference updates have mostly been followed by negative price reactions, with only one out of five similar news items seeing a positive 24-hour move.

Recent Company History

Over the last several months, ATNM’s news flow has centered on Ac-225 radioconjugates (ATNM-400) and Actimab-A data at AACR and SNMMI. Updates on pan-tumor efficacy, mutation-agnostic mechanisms, and upcoming conference presentations generally read positively but often saw negative next-day moves (e.g., -10.86% on Apr 22, 2026). Today’s CAR optimization data fits the pattern of platform-focused preclinical news, but the stock’s current gain contrasts with several prior selloffs.

Key Terms

chelator-to-antibody ratio, radioconjugates, pharmacokinetics, biodistribution, +1 more
5 terms
chelator-to-antibody ratio medical
"Optimization of chelator-to-antibody ratio (CAR) is a key design parameter"
The chelator-to-antibody ratio (CAR) is the average number of small linking molecules attached to each antibody that hold a drug or radioactive payload. Think of the antibody as a carrier and the chelators as hooks that let it carry multiple “packages”; the CAR affects how potent the therapy is, how predictable and safe dosing will be, and how consistently it can be manufactured and regulated—factors that directly influence clinical success and investor risk.
radioconjugates medical
"next-generation radioconjugates, presenting tunable levers Actinium is utilizing"
Radioconjugates are medicines made by attaching a tiny amount of radioactive material to a molecule that homes in on specific cells, like a guided missile carrying a beacon or a payload to a specific target. For investors, they matter because they combine diagnostic and therapeutic value, can command premium pricing, require specialized manufacturing and regulatory approval, and trial or approval outcomes can quickly change a company’s revenue prospects and risk profile.
pharmacokinetics medical
"improves Tumor Targeting and Pharmacokinetics of Actinium-225 Radioconjugates"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
biodistribution medical
"directly influences radiolabeling efficiency, antigen binding, internalization, and biodistribution."
Biodistribution is the map of where a drug, vaccine, or diagnostic agent travels and accumulates inside the body after administration. Investors care because where a product ends up affects how well it works, what side effects it may cause, and whether regulators will approve it—similar to tracking dye in a plumbing system to find leaks or blockages; unexpected destinations can raise safety, cost, and market-adoption risks.
radiochemical purity medical
"Both conjugates remained stable over 7 days (radiochemical purity above 97%)"
Radiochemical purity is the share of radioactivity in a radiopharmaceutical sample that exists as the intended radioactive molecule, rather than as unwanted breakdown products or contaminants. Think of it like the percentage of a cake that is the correct flavor: lower purity means less reliable performance, shorter usable life, and higher regulatory and production risk, so investors use it as a measure of product quality, manufacturing control, and commercial viability.

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  • Optimization of chelator-to-antibody ratio (CAR) is a key design parameter for next-generation radioconjugates, presenting tunable levers Actinium is utilizing to engineer more effective drug candidates
  • Optimized CAR improved tumor targeting, internalization, and pharmacokinetics of 225Ac-labeled antibodies
  • Lower-CAR conjugates preserved tumor targeting while reducing off-target liver and spleen uptake, supporting a wider therapeutic window that may enable higher, safer dosing
  • Findings reinforce Actinium's proprietary radiochemistry expertise and directly support the Company's broader radioconjugate pipeline a capability that applies to every program from the platform

NEW YORK, June 1, 2026 /PRNewswire/ -- Actinium Pharmaceuticals, Inc. (NYSE American: ATNM) (Actinium or the Company), a pioneer in the development of targeted radiotherapies, on May 31, 2026 presented new radiochemistry data at the Society of Nuclear Medicine and Molecular Imaging (SNMMI) 2026 Annual Meeting taking place in Los Angeles, California.

The poster presented a systematic evaluation of chelator-to-antibody ratio (CAR) optimization for Actinium-225 (225Ac)-labeled antibody radioconjugates, a critical but often underappreciated design parameter that directly influences radiolabeling efficiency, antigen binding, internalization, and biodistribution. The findings reinforce a proprietary radiochemistry capability that underpins the Company's broader pipeline. Practically, CAR governs how many radioactive payloads each tumor-seeking antibody carries. Too few a payload causes a radioconjugate drug to under deliver, too many and the antibody loses its aim and leaks dose into healthy tissue. Therefore, identifying the optimal ratio is what separates a technically active therapy from one that can be dosed effectively and safely.

Sandesh Seth, Actinium's Chairman and CEO, said, "Our CAR optimization data underscore the depth of our radiochemistry expertise and our focus on maximizing therapeutic index, which we believe is a key differentiator of our platform. Getting the chelator-to-antibody ratio right is fundamental to preserving the biological integrity of an antibody while enabling robust 225Ac labeling and favorable pharmacokinetics. These findings have direct implications for the design of next-generation radioconjugates, and reinforce a radiochemistry advantage that supports successful clinical translation across our pipeline."

Highlights from the SNMMI 2026 Poster Presentation
Poster Titled: Optimizing Chelator-to-Antibody Ratio Improves Tumor Targeting and Pharmacokinetics of 225Ac-Labeled Antibodies

Optimizing the chelator-to-antibody ratio (CAR) is a critical but often underappreciated design parameter in antibody-based radiopharmaceuticals. Actinium's scientists conducted a systematic evaluation of CAR for 225Ac-labeled antibody radioconjugates, with findings directly applicable to the development of Actinium's radiopharma pipeline:

  • Antibody-DOTA conjugates spanning CAR 0.7–9 were prepared. CAR ≥1.7 enabled robust 225Ac labeling, while CAR 0.7 was insufficient. This establishes the minimum loading needed to carry an effective radioactive dose
  • Antigen binding stayed high at low CAR (91–98% at CAR 0.7–3.2) but fell at high CAR (79–85% at CAR 7–9), and low-CAR conjugates internalized more, keeping more of the antibody functional. Median Fluorescence Intensity (MFI) is a proxy for binding or antigen affinity retention. Findings suggest overloading the antibody degrades its ability to find and enter cancer cells
  • In vivo, both conjugates showed comparable tumor uptake and sustained retention through 192 h, but the low-CAR (2.5) conjugate significantly reduced liver and spleen uptake, providing a basis for a wider therapeutic index
  • Both conjugates remained stable over 7 days (radiochemical purity above 97%), showing that CAR can be optimized for performance without compromising manufacturability or clinical supply. Safety and targeting gains can come with no manufacturing trade-off
  • A wider therapeutic index could allow more dose to reach the tumor at a given level of safety, a proprietary radiochemistry framework Actinium is applying to de-risk its broader pipeline resulting in lower technical risk across the portfolio

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

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/actinium-pharmaceuticals-presents-new-radiochemistry-data-at-snmmi-2026-demonstrating-that-car-optimization-improves-tumor-targeting-and-pharmacokinetics-of-actinium-225-radioconjugates-302786571.html

SOURCE Actinium Pharmaceuticals, Inc.

FAQ

What radiochemistry findings did Actinium (ATNM) present at SNMMI 2026 about chelator-to-antibody ratio?

Actinium presented data showing chelator-to-antibody ratio (CAR) strongly influences Actinium-225 radioconjugate labeling, targeting, and pharmacokinetics. According to Actinium, systematic CAR optimization affected radiolabeling efficiency, antigen binding, internalization, and biodistribution, supporting a framework to engineer more effective, targeted radiopharmaceutical drug candidates across its radioconjugate pipeline.

How does chelator-to-antibody ratio optimization impact Actinium-225 tumor targeting in Actinium (ATNM) research?

Optimized chelator-to-antibody ratio preserved strong tumor targeting while changing off-target organ uptake. According to Actinium, both low- and high-CAR Actinium-225 conjugates showed comparable tumor uptake and retention through 192 hours, but low-CAR constructs reduced liver and spleen uptake, supporting a potentially wider therapeutic index for future radioconjugates.

What CAR range did Actinium (ATNM) evaluate for Actinium-225 antibody radioconjugates at SNMMI 2026?

Actinium evaluated antibody-DOTA conjugates across a chelator-to-antibody ratio range of 0.7 to 9. According to Actinium, CAR values of at least 1.7 enabled robust Actinium-225 labeling, while CAR 0.7 was inadequate, helping define minimum loading needed to deliver an effective radioactive payload per antibody.

How did chelator-to-antibody ratio affect antigen binding and internalization in Actinium (ATNM) data?

Lower chelator-to-antibody ratios maintained higher antigen binding and internalization versus high-CAR constructs. According to Actinium, binding remained 91–98% at CAR 0.7–3.2 but dropped to 79–85% at CAR 7–9, while low-CAR conjugates internalized more, suggesting overloading can reduce an antibody’s ability to find and enter cancer cells.

What did Actinium (ATNM) report about safety and therapeutic index from CAR optimization of Actinium-225 radioconjugates?

Actinium reported that low-CAR Actinium-225 conjugates lowered liver and spleen uptake while keeping tumor targeting. According to Actinium, this supports a wider therapeutic index that may allow higher or safer dosing, and this radiochemistry framework is being applied to de-risk programs across its broader radioconjugate pipeline.

Did Actinium (ATNM) observe any manufacturability issues when optimizing CAR for Actinium-225 radioconjugates?

Actinium observed no manufacturability trade-offs when optimizing chelator-to-antibody ratio for its radioconjugates. According to Actinium, both low- and high-CAR Actinium-225 conjugates maintained radiochemical purity above 97% over seven days, indicating CAR can be tuned for performance without compromising stability or clinical supply considerations.