Cellectar Biosciences to Present at the Oppenheimer 35th Annual Healthcare Life Sciences Conference

On February 5, 2025 Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage clinical biopharmaceutical company focused on the discovery, development and commercialization of drugs for the treatment of cancer, reported that members of its management team will present an overview of the company at the upcoming Oppenheimer 35th Annual Healthcare Life Sciences Conference being held virtually (Press release, Cellectar Biosciences, FEB 5, 2025, View Source [SID1234650051]). Details are as follows:

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Date: Wednesday, February 12, 2025
Time: 12:00 PM Eastern Time
Webcast: Click HERE

A replay of the corporate presentation will be available on the Events section of the company’s investor relations website.

Carisma Therapeutics to Participate in Oppenheimer 35th Annual Healthcare Life Sciences Conference

On February 5, 2025 Carisma Therapeutics Inc. (Nasdaq: CARM) ("Carisma" or the "Company"), a leader in macrophage-focused therapeutics, reported that Steven Kelly, President and Chief Executive Officer, will participate in the Oppenheimer 35th Annual Healthcare Life Sciences Conference on Tuesday, February 11 at 4:40 pm ET (Press release, Carisma Therapeutics, FEB 5, 2025, View Source [SID1234650067]).

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An audio webcast of the event will be available on the Company’s Investor Events section of the Investor Relations webpage and will be archived for a limited time following the event.

US Patent Granted Titled: Bifunctional Compositions for the Treatment of Cancer

On February 5, 2025 Armaceutica reported US patent granted titled: Bifunctional Compositions for the Treatment of Cancer (Press release, Armaceutica, FEB 5, 2025, View Source [SID1234650068]). This drug, which is often used to treat malaria, is being repurposed by Armaceutica, Inc. to treat various types of cancer.

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Renato Aguilera, Ph.D. and Biology Professor and cancer researcher at the University of Texas at El Paso, published data demonstrating that the drug (pyronaridine, or PND) kills various types of cancer cells.3

Pyronaridine was shown to preferentially kill certain types of leukemia, lymphoma, melanoma, multiple myeloma, lung, ovarian, and breast cancer cells while limiting off-target toxicities in normal, healthy cells.3 That is, pyronaridine had reduced effects on non-cancerous cells with a favorable selective cytotoxicity index (SCI), as compared with cancerous cells.3

Dr. Aguilera’s studies revealed that pyronaridine inhibits the activity of a critical enzyme (topoisomerase II) required for DNA replication and cancer cell division.4

Studies on mice with metastatic human breast cancer showed the group that received pyronaridine had smaller tumor volumes (P<0.0001) and increased longevity than control mice.4 A study on dogs with cancer showed pyronaridine reduced tumor volumes and increased longevity.1 In one case a lymphoma tumor shrunk by 70%.1 A pilot study on terminally-ill humans with late-stage cancers of the breast, lung and liver; pyronaridine appears to have increased longevity.1

The company’s CEO, Ernest Armstrong, said: "Pyronaridine represents a disruptive breakthrough relative to other cancer therapies. Pyronaridine has been proven safe and effective for malaria in at least four phase 3 studies and is an approved drug in parts of Asia and Africa." 2

Patent offices in Australia, Canada, EU, Israel, Japan, Malaysia, Mexico, Philippines, Russia, Thailand and the UK have granted patents corresponding to U S Patent No.: 12,201,626.

If you or a loved one has ever been treated with chemotherapy, you’ll understand how devastating the side effects can be.

Dr. Aguilera stated: "If the drug were available in the US and approved as an anti-cancer treatment, I would take it in an instant, if I came down with cancer."

Armaceutica, Inc. is a US-based pharmaceutical company focused on low-toxicity cancer treatments. Armaceutica is seeking a partner to develop pyronaridine into an approved drug for cancer, a process that will take several years.

References: 1US Patent No.: 12,201,626, Jan. 21, 2025. 2Croft et al., Malaria Journal 2012, 11:270. 3 Villanueva PJ, et al., PLOS One, 5 Nov 2018, 13(11):e0206467. 4 Villanueva PJ, et al., Clinical Cancer Drugs 2021, 8:50-56.

FDA Accepts Integral Molecular’s Membrane Proteome Array™ Qualification Plan, Advancing the Platform for Approval as a Drug Development Tool

On February 5, 2025 Integral Molecular, a leader in antibody discovery technologies, reported that the FDA has accepted their Membrane Proteome Array (MPA) Qualification Plan for advancement as a Drug Development Tool (DDT) to assess antibody binding specificity (Press release, Integral Molecular, FEB 5, 2025, View Source [SID1234650053]). Antibody drug developers already routinely include MPA data in regulatory packages, and qualification as a DDT will allow them to further rely on the MPA in the approval process. Integral Molecular’s MPA is the industry-leading technology for antibody specificity testing and is the only specificity platform under FDA consideration as a DDT.

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Learn more about the Membrane Proteome Array, and how it enables the precise identification of off-target binding interactions

Non-specific drug binding is a significant cause of adverse events in patients that can lead to severe complications or even death, and early specificity testing can de-risk drug development and enhance patient safety. Recent research has demonstrated that up to one-third of antibody drugs exhibit non-specific binding to unintended targets.

The MPA assesses binding across ~6,000 structurally intact membrane proteins and is the only platform of its kind that screens membrane proteins in their native conformation. The MPA has been used to screen over 2,000 preclinical antibody therapeutics for customers worldwide, and MPA specificity data has been accepted by regulatory bodies globally, including the FDA, EMA, and NMPA.

"This milestone towards MPA qualification reflects the continued dedication of our team to set a new standard in testing antibody drug specificity. Our continued improvements to the MPA—including statistical analyses, bioinformatic comparisons, and enhanced quality systems—have been critical to our qualification plan and have supported ISO 9001 certification of our processes. We thank the FDA for their confidence in our approach and commitment to advancing the safety of biologics."

-Benjamin Doranz, CEO, Integral Molecular

The MPA is progressing toward DDT qualification under the FDA’s ISTAND Pilot Program, which promotes Innovative Science and Technology Approaches for New Drugs. As part of this process, Integral Molecular has been invited to submit a Full Qualification Plan (FQP) for the MPA, which is the final step in achieving DDT status.

2024 Annual Report

On February 5, 2025 Boston Scientific reported its financial annual report of the year 2024 (Presentation, Boston Scientific, FEB 5, 2025, View Source [SID1234652112]).

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