Actinium Pharmaceuticals (NYSE AMERICAN: ATNM) stock is doing something most of its peers aren't: rallying. In fact, since the start of Q4, ATNM shares are currently 48% higher than where they started. Keep in mind that the move is also coming at a time when broader markets, especially biotech, are again weakening. But when markets function correctly, news can be the difference between under and over-performing market moves. That appears to be the case here, and with ATNM providing plenty of reasons to support its bullish momentum, scoring multi-month highs and staying on pace to potentially breach 52-week highs sooner than later may be the path of least resistance. (*share price difference calculated from period starting 10/1/22 to 12/06/22 Yahoo!Finance, 09:40am EST)

That's not an overly bullish presumption. By all measures, recent updates indicate that ATNM is scoring the type of data needed to bring its potential best-in-class drug treatments to market. In ATNM’s case, being different is good, and that's exactly why investors have reasons to be interested in the company and its science. They are, after all, targeting a massive need to provide treatment opportunities to patients resistant to or untreatable by current cancer treatment regimens and therapeutics. But the better news is that results are indicating ATNM can do more than “target” these indications; they are showing a unique ability to effectively treat them with targeted radiotherapies. That could translate to frontline opportunities, a potentially enormous revenue stream, and best of all, a life-saving treatment option for patients.

It’s an appealing opportunity that’s attracting the attention of all involved parties. Investors appreciate the stock's gains, ATNM enjoys being on the verge of validating years of clinical work, and patients may be closer to receiving life-saving treatments made available for the first time ever. Thus, the phrase “win-win-win proposition” may be more than an appropriate analysis in ATNM's case; it's one they can deliver.

Phase 3 Clinical Data Update Imminent

Investors certainly believe that could be the case. They have been bidding shares higher following a corporate update that showed they are on schedule to release additional clinical trial updates this quarter. Now that December has been ushered in, those updates could be imminent. And what's the best fuel for stocks that already benefit from a bullish tailwind? More good news. Thankfully, that's precisely what ATNM and its investors may get. In fact, if precedent is met, ATNM is about to add to prior clinical data that has already separated its clinical trial candidates from other potential treatments. Not only is the data compelling; it’s showing an ability to save lives, which could validate its potential as a frontline treatment targeting indications needing improved standards of care. In some cases, ATNM will do more than improve the standard of care. By developing a drug leading to survival, they can create a new one.

An update last month suggests they are on track to meet that goal. A significant growth catalyst could be on the horizon, with ATNM highlighting that data from its ongoing late-stage clinical trials to treat patients resistant to particular cancer treatments is cumulative in nature. In other words, an already promising drug candidate is apparently getting better. Moreover, with topline data from its Phase 3 SIERRA trial expected by the end of this month, investors won't be waiting long to score what could be a transformative achievement for the company. Remember, this update would be more than a clinical milestone reached; it may be the one that presents the validating data required to pave a road to near-term regulatory approvals and bring life-saving therapeutics to patients with no current treatment options.

Recent trading activity indicates investors expect the best. They have reasons to believe so, noting prior clinical updates showing the potential for Iomab-B to become a standard of care treatment for relapsed or refractory (r/r) acute myeloid leukemia (AML) patients with active disease. The drug and treatment’s differences are its advantages, with the primary one being that ATNM's Iomab-B's targeted radiotherapy is alone in giving patients with active AML an opportunity to receive potentially curative bone marrow transplants (BMT). Without it, at least in most cases, the disease would need to be in remission. The even better news is that Iomab-B therapy may significantly lessen the adverse effects of conventional non-targeted chemotherapy, which is debilitating mentally and, more so, physically due to the damage it can cause to healthy tissues.

Contributing to the optimism is that Phase 3 Iomab-B is on track to meet its trial endpoints, including scoring positive data comparing outcomes between elderly patients with active r/r AML who receive Iomab-B and subsequent BMT with those who receive a physician's choice of salvage therapy. The overarching endpoint for the SIERRA trial is durable Complete Remission (dCR) of at least 180 days; secondary endpoints will examine Overall Survival and Event-Free Survival. Recalling precedent, they are again in play.

Precedent is Feeding Bullish Appetites

And few argue against another set of positive trial news getting published. If all does post as expected, ATNM will strengthen Iomab-B's resume by adding to trial data presented at the annual meetings of the American Society for Transplantation & Cellular Therapy and the Center for International Blood & Marrow Transplant Research. That presentation showed data indicating a 5x greater difference in the number of patients potentially evaluable for the dCR primary endpoint at 100-days post-BMT in the Iomab-B arm compared to the control arm at maximum enrollment. Most impressive, the data demonstrated that 100% (66/66) of patients receiving Iomab-B accessed BMT and engrafted without delay, and 100% (40/40) of patients crossing over to receive Iomab-B proceeded to BMT. Compared to the control arm, patients receiving Iomab-B also experienced 5% to 10% lower rates of 100-day, non-relapse transplant-related mortality. There's more good news.

Iomab-B patients experienced a sepsis rate of only 5.3% compared to the control arm's rate of 23.7% - a statistically significant advantage with life-saving implications. Moreover, as the only CD45-targeting drug candidate in Phase 3 clinical development, Iomab-B has earned an Orphan Drug Designation from the U.S. Food and Drug Administration and the European Medicines Agency. Those designations can accelerate the approval process, attract business partnerships, and help fund ongoing trials. ATNM is deserving of all three, especially with Iomab-B being the only known route to a bone marrow transplant for patients with active disease.

Yes, there are currently nine approved drugs for AML. However, none of those are curative. Therefore, the trial update expected this month could profoundly impact patients who need an alternative to current treatment options. It could also make the recent rally in share price the precursor of higher gains to come. Actually, there's plenty more in the pipeline to support higher valuations.

Pipeline Potential Accretive To Bullish Sentiment

While ATNM's Phase 3 SIERRA Trial of Iomab-B is catching the current headlines, additional data from other trial interests are expected by year’s end. That includes overall survival data from its Actimab-A CLAG-M combination trial as a potential therapy for patients with advanced AML using the radioisotope’s differentiated mechanism of action in combination with other therapeutic modalities. Actimab-A is the only CD33-targeting radiotherapy under development, and like its other data sets, it is providing ATNM and its investors with reasons to be encouraged about its potential.

Data from the Phase 1 trial showed a 72% MRD negativity rate in patients receiving Actimab-A + CLAG-M, a substantial improvement over the 39% MRD negativity rate in patients treated with CLAG-M alone. Further, the trial reported no 30-day mortality, with an 80% overall response rate (CR/CRp/MLFS) in patients receiving less than four lines of prior therapy with 10 complete remissions across all four dose cohorts. If the data released in the coming weeks remains as potent as it has previously, it could position ATNM to bring multiple life-changing therapies to market. If that's the endgame in the crosshairs, expect current prices to be short of an appropriate valuation. As it is, with ATNM being a late-stage Phase 3 company, the disconnect is already significant.

Balance Sheet To Advance Quickly

It's made even wider knowing that ATNM is well-capitalized to advance its trials and ambitions. The company reported having roughly $116.3 million in cash and cash equivalents as of June 30, 2022 – an impressive amount for a small-cap biotech company. Better yet, new deals could strengthen that position.

For instance, Actinium licensing the EUMENA commercial rights for Iomab-B to Immedica AB brings significant revenue-generating potential. The licensing agreement, which included a $35 million upfront payment from Immedica, could be worth $417 million after sales milestones and mid-20% royalties. Immedica is an independent pharmaceutical company operating in Europe and the Middle East. Its main objective is to market treatments for rare diseases and specific niches in the healthcare industry, making the company a perfect fit for ATNM's offerings. The commercial licensing agreement offers a way for ATNM to build its international presence and treat a more significant proportion of the 21,000 patients diagnosed with AML each year.

Actinium added that its current cash and cash equivalents can sufficiently fund its operations through mid-2025, allowing the company to continue its research and seek out accretive partnerships. There's still more to like about the ATNM story. 

Patents, Partnerships, Profits

Foremost is that by capitalizing upon its proprietary technologies and clinical experience, ATNM is diligently working to bring additional and potentially unrivaled targeted radiotherapy treatments to the market. Its programs include evaluations of therapies that target and deplete specific cancer and immune cells to allow for a safe bone marrow transplant, among other gene and adoptive cell therapies. The company is a leading developer of Ac-225-based therapies and has amassed over 190 patents within its intellectual property portfolio. ATNM has presented considerable research regarding its Ac-225 therapies that target CD38 and HER3, as well as the first CD47 immune checkpoint targeted radiotherapy combinations with HER2 in solid tumors and CD33 in blood cancers.

Further, the versatility of ATNM's technologies and research candidates have led to multiple partnerships to accelerate the development of its innovative therapies. These collaborations include a partnership with AVEO Pharmaceuticals (NASDAQ: AVEO) on HER3-targeting radiotherapies for solid tumors, a collaboration with Astellas Pharma (TSE: 4503) focused on solid tumor theranostics, and studies with EpicentRx on CD47 immune checkpoint targeted radiotherapy combinations. 

ATNM's partnerships and internal research projects have generated substantial momentum that could carry its transformative treatments to market. Also, given that major pharmaceutical companies like Pfizer (NYSE: PFE) and Bristol-Myers Squibb (NYSE: BMY) prefer to acquire rather than develop, even more deals could be on the horizon.

Q4 Milestones Into Catalysts

Indeed, heading into the final weeks of Q4, it looks like all systems are a go for ATNM to add to its case of bringing curative therapies to cancer patients untreatable by current methods. Keep in mind, too, that ATNM’s therapeutic candidates and research collaborations are rapidly moving through the development pipeline with substantial progress updates likely in the queue. And with designations that could fuel approvals, these treatment candidates could reach the market and patients faster than many think. That combination is a potent recipe for share price appreciation.

In fact, ATNM's current share price, even after a recent bullish move, is still attractively priced. Considering that prior updates and data provide an excellent precedent supporting the case for more of the same to come, it's compelling from a valuation perspective too. And with confirmatory data potentially in the queue, the ATNM bulls may do more than run the stock higher: they may stampede it. Given that ATNM may be on the verge of delivering revolutionary therapies for diseases with poor treatment availability, doing so would be more than timely; it would be appropriate.

Disclaimers: Shore Thing Media, LLC. (STM, Llc.) is responsible for the production and distribution of this content. STM, Llc. is not operated by a licensed broker, a dealer, or a registered investment adviser. It should be expressly understood that under no circumstances does any information published herein represent a recommendation to buy or sell a security. Our reports/releases are a commercial advertisement and are for general information purposes ONLY. We are engaged in the business of marketing and advertising companies for monetary compensation. Never invest in any stock featured on our site or emails unless you can afford to lose your entire investment. The information made available by STM, Llc. is not intended to be, nor does it constitute, investment advice or recommendations. The contributors may buy and sell securities before and after any particular article, report and publication. In no event shall STM, Llc. be liable to any member, guest or third party for any damages of any kind arising out of the use of any content or other material published or made available by STM, Llc., including, without limitation, any investment losses, lost profits, lost opportunity, special, incidental, indirect, consequential or punitive damages. Past performance is a poor indicator of future performance. The information in this video, article, and in its related newsletters, is not intended to be, nor does it constitute, investment advice or recommendations. STM, Llc. strongly urges you conduct a complete and independent investigation of the respective companies and consideration of all pertinent risks. Readers are advised to review SEC periodic reports: Forms 10-Q, 10K, Form 8-K, insider reports, Forms 3, 4, 5 Schedule 13D. For some content, STM, Llc., its authors, contributors, or its agents, may be compensated for preparing research, video graphics, and editorial content. STM, LLC has been compensated up to five-thousand-dollars cash via wire transfer by a third party to produce and syndicate content for Actinium Pharmaceuticals, Inc.. for a period of one week. As part of that content, readers, subscribers, and website viewers, are expected to read the full disclaimers and financial disclosures statement that can be found on our website. The Private Securities Litigation Reform Act of 1995 provides investors a safe harbor in regard to forward-looking statements. Any statements that express or involve discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, goals, assumptions or future events or performance are not statements of historical fact may be forward looking statements. Forward looking statements are based on expectations, estimates, and projections at the time the statements are made that involve a number of risks and uncertainties which could cause actual results or events to differ materially from those presently anticipated. Forward looking statements in this action may be identified through use of words such as projects, foresee, expects, will, anticipates, estimates, believes, understands, or that by statements indicating certain actions & quote; may, could, or might occur. Understand there is no guarantee past performance will be indicative of future results. Investing in micro-cap and growth securities is highly speculative and carries an extremely high degree of risk. It is possible that an investors investment may be lost or impaired due to the speculative nature of the companies profiled. 

Media Contact
Company Name: STM, LLC.
Contact Person: Michael Thomas
Email: contact@primetimeprofiles.com
Phone: 917-773-0072
Country: United States
Website: https://primetimeprofiles.com/