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(NYSE American: ATNM) Makes A Major Green Statement In Pre-Market, Tops My Watchlist Wednesday
March 26th
Greetings Readers,
Actinium Pharmaceuticals, Inc. (NYSE American: ATNM) continues to hold the top spot on my watchlist early Wednesday.
Making green moves ahead of the bell, ATNM could generate some serious breakout buzz based on recent chart movements that have put it above 4 key technical levels while also seeing it hit a high of $2.23 yesterday.
It's also coming off some fresh news Monday that is still making the rounds.
With the opening bell about to pop off, my full focus will be on (NYSE American: ATNM) this morning.
Be on the lookout for updates early and take a moment to review my initial report below.
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It's Wednesday morning and there's zero time to waste.
I've been tracking a company that's been on a tear and displaying serious breakout potential.
In the last couple weeks, several positive press releases have been shared by this company painting a positive trajectory in 2025 and beyond.
But it's not just that... This profile has moved above several key lines of potential chart support.
If support starts growing significantly at those levels, it could help this profile gain enough momentum to try and track down previous highs.
Another highlight? How about an analyst target pointing to triple-digit potential upside from its closing valuation Tuesday?
Listen. There's a lot to go over, so clear your plate and pay close attention.
Actinium Pharmaceuticals, Inc. (NYSE American: ATNM) is a pioneer in targeted radiotherapy for oncology.
The company is advancing Actimab-A, a CD33-targeting therapeutic designed as a backbone therapy for acute myeloid leukemia (AML) and other myeloid malignancies.
Actimab-A leverages Actinium-225 (Ac-225), a mutation-agnostic alpha-emitter radioisotope, to deliver targeted radiotherapy directly to cancer cells.
Key Developments For Actinium Pharmaceuticals
- Actimab-A has shown high rates of Complete Remission (CR) and measurable residual disease (MRD) negativity in relapsed and refractory AML (r/r AML) patients.
- The candidate is advancing to a pivotal Phase 2/3 clinical trial, with potential implications for significantly improved patient outcomes.
- Actinium is working with the National Cancer Institute (NCI) under a Cooperative Research and Development Agreement (CRADA) to expand Actimab-A's applications.
Beyond AML, Actinium Pharmaceuticals, Inc. is also developing Actimab-A as a combination therapy for solid tumors, particularly in combination with PD-1 checkpoint inhibitors, such as:
- KEYTRUDA® (Merck & Co.)
- OPDIVO® (Bristol Myers Squibb)
Breakthrough Potential In The Immuno-Oncology Market
Actinium Pharmaceuticals, Inc. recently announced a clinical trial program designed to evaluate the combination of Actimab-A with PD-1 inhibitors in treating solid tumors.
The rationale behind this program lies in tackling an emerging challenge in cancer treatment:
- Myeloid-Derived Suppressor Cells (MDSCs), which accumulate in the tumor microenvironment, are known to reduce the effectiveness of PD-1 inhibitors like KEYTRUDA® and OPDIVO®.
- Actimab-A selectively targets and depletes CD33-expressing MDSCs, a novel mechanism that could enhance the efficacy of PD-1 therapies.
- If successful, this approach could open the door to a massive market in immuno-oncology with significant growth potential.
The Competitive Advantage
Actinium Pharmaceuticals, Inc. is working to establish itself as a key player in next-generation radiotherapy, backed by a strong intellectual property portfolio and a growing pipeline of targeted therapies.
The company holds 230 patents and patent applications, including critical protections related to the production of Actinium-225 (Ac-225) in a cyclotron—an essential component of its radiotherapy platform.
Beyond its intellectual property, Actinium Pharmaceuticals, Inc. is advancing treatments for both hematologic and solid tumors.
Its pipeline includes Actimab-A, a targeted radiotherapy designed for acute myeloid leukemia (AML), as well as ongoing research into expanding its use in combination with PD-1 inhibitors for solid tumors.
The company is also progressing with its Iomab-B program, which is being developed as an induction and conditioning agent for patients undergoing bone marrow transplants in relapsed or refractory AML.
Actinium Pharmaceuticals' Pipeline
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