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Cellectar Biosciences Inc - CLRB STOCK NEWS

Welcome to our dedicated page for Cellectar Biosciences news (Ticker: CLRB), a resource for investors and traders seeking the latest updates and insights on Cellectar Biosciences stock.

About Cellectar Biosciences Inc.

Cellectar Biosciences Inc. (NASDAQ: CLRB) is a late-stage clinical biopharmaceutical company dedicated to advancing the treatment of cancer through its proprietary Phospholipid Drug Conjugate™ (PDC) platform. This innovative technology is designed to deliver therapeutic payloads directly to cancer cells, offering enhanced efficacy and reduced off-target effects. By leveraging its PDC platform, the company aims to address significant unmet medical needs in oncology while improving patient outcomes.

Core Technology: The PDC Platform

Cellectar’s PDC platform is based on proprietary phospholipid ether analogs, which demonstrate highly selective uptake and retention in cancer cells. This precision-targeting capability enables the development of therapies that minimize damage to healthy tissue, making it a promising approach for both therapeutic and diagnostic applications. The platform supports the delivery of various oncologic payloads, including radioisotopes, chemotherapeutics, and other therapeutic agents.

Pipeline and Lead Product Candidates

The company’s product pipeline includes a diverse range of assets designed to target hematologic malignancies and solid tumors:

  • Iopofosine I 131: A small-molecule PDC utilizing iodine-131, a cytotoxic radioisotope, to target and destroy cancer cells. This lead asset is under evaluation in clinical trials for multiple indications, including Waldenstrom’s macroglobulinemia (WM), multiple myeloma, and central nervous system lymphoma. It has received Orphan Drug and Fast Track Designations from the U.S. FDA for various cancer indications.
  • CLR 121225: An actinium-225-based alpha-emitting radioconjugate targeting solid tumors such as pancreatic and triple-negative breast cancers. This program aims to leverage the precision of alpha emitters for enhanced efficacy in difficult-to-treat cancers.
  • CLR 121125: An iodine-125 Auger-emitting radioconjugate with applications in triple-negative breast, lung, and colorectal cancers. Auger emitters offer unparalleled precision, delivering therapeutic effects at the subcellular level.

Strategic Focus and Market Position

Cellectar’s strategy combines internal drug development with external collaborations to maximize the potential of its PDC platform. By partnering with other biopharmaceutical companies, Cellectar expands the applicability of its technology while diversifying its revenue streams. The company’s focus on radiopharmaceuticals positions it within a niche but growing segment of the oncology market, where demand for targeted therapies is increasing.

Industry Challenges and Opportunities

Operating in the competitive oncology sector, Cellectar faces challenges such as regulatory approvals, supply chain complexities for rare isotopes, and significant capital requirements for clinical development. However, its proprietary platform, coupled with a robust pipeline and strategic collaborations, provides a strong foundation for addressing these challenges. The company’s focus on unmet medical needs and orphan drug markets further enhances its growth potential.

Commitment to Innovation

With a mission to revolutionize cancer treatment, Cellectar continues to advance its pipeline and explore new applications for its PDC platform. Its dedication to innovation, combined with a strategic approach to development and commercialization, underscores its potential to make a lasting impact in oncology.

Rhea-AI Summary

Cellectar Biosciences (NASDAQ: CLRB) announced the grant of a new patent titled "Phospholipid-Ether Analogs as Cancer-Targeting Drug Vehicles" by patent authorities in Eurasia, Australia, and Mexico. This patent provides protection for their phospholipid-ether (PLE) analogs used in combination with various small molecule chemotherapies. CEO James Caruso highlighted the patent's role in enhancing their phospholipid drug conjugate (PDC) platform, aimed at improving drug efficacy and safety in cancer treatment. Their lead candidate, CLR 131, is in pivotal clinical studies for hematologic cancers.

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On March 11, 2021, Cellectar Biosciences (NASDAQ: CLRB) announced that its CEO, James Caruso, will present at two upcoming conferences. The Oppenheimer 31st Annual Healthcare Conference is scheduled for March 16, 2021, at 8:00 am ET, with opportunities for 1x1 meetings. The Maxim Group 2021 Emerging Growth Virtual Conference takes place from March 17-19, 2021. Cellectar focuses on cancer treatment drug development, particularly through its Phospholipid Drug Conjugate™ platform.

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Cellectar Biosciences (NASDAQ: CLRB) announced on March 9, 2021, that the Japan Patent Office granted patent number 6832861 for its phospholipid-ether (PLE) analogs, enhancing its intellectual property portfolio. This patent secures composition of matter and use for these analogs in combination with various small molecule chemotherapeutics, bolstering their Phospholipid Drug Conjugates™ (PDCs™) franchise. Lead candidate CLR 131 continues to progress in clinical studies for both adult and pediatric cancer indications.

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Cellectar Biosciences (NASDAQ: CLRB) announced participation in upcoming conferences for 1x1 meetings. The H.C. Wainwright Global Life Sciences Conference will take place on March 9-10, 2021, and the Roth Capital Partners 33rd Annual Conference from March 15-17, 2021. Interested parties can schedule meetings through provided links. Cellectar focuses on developing cancer-targeting drugs using its Phospholipid Drug Conjugate™ (PDC) platform, including its lead product CLR 131, currently in pivotal trials for various cancers.

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Cellectar Biosciences (NASDAQ: CLRB) reported its 2020 financial results and key developments. The company received Orphan Drug Designation from the European Commission for CLR 131 in Waldenstrom’s macroglobulinemia, facilitating reduced fees and market exclusivity. CLR 131 is undergoing pivotal trials for WM, with a primary endpoint focused on response rates. Cellectar successfully closed a $45 million public offering and highlighted CLR 131's potential in treating inoperable brain tumors. As of December 31, 2020, cash and cash equivalents reached $57.2 million, supporting operations for at least another 12 months.

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Cellectar Biosciences (NASDAQ: CLRB), a biopharmaceutical firm focused on cancer treatment, announced that its CEO, James Caruso, will present a company overview at the virtual 2021 BIO CEO & Investor Digital Conference from February 16-18, 2021. The presentation will be available for on-demand viewing starting February 12, 2021, at 12:00 PM ET. Cellectar's proprietary Phospholipid Drug Conjugate™ (PDC) platform aims to improve cancer therapies, with CLR 131 currently in clinical studies targeting hematologic malignancies. Replays will be accessible on the company’s website.

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Cellectar Biosciences (NASDAQ: CLRB) announced a positive opinion from the European Medicines Agency for CLR 131's orphan designation to treat Waldenstrom’s Macroglobulinemia. This designation grants significant benefits, including 10 years of market exclusivity in the EU. CLR 131 demonstrated a 100% overall response rate with durable effects after treatment. The company is advancing a pivotal trial for CLR 131 in relapsed/refractory patients.

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Cellectar Biosciences (NASDAQ: CLRB) has initiated a pivotal trial for CLR 131 targeting Waldenstrom’s macroglobulinemia (WM), a rare and incurable lymphoma. This global, single-arm expansion cohort is part of the Phase 2 CLOVER-1 study and will enroll 50 patients who have failed prior treatments, including BTK inhibitors. The trial aims to assess the response rate, with interim evaluations conducted by an independent monitoring committee. CLR 131 has received FDA Fast Track and Orphan Drug designations, enhancing its pathway for commercialization.

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On December 28, 2020, Cellectar Biosciences (NASDAQ: CLRB) completed an underwritten public offering of common stock, raising approximately $24.5 million at $1.35 per share. Concurrently, a private placement of Series D convertible preferred stock generated about $20.5 million. Each share of Series D can convert into 10,000 common shares upon stockholder approval as per Nasdaq rules. This funding will support Cellectar's cancer drug development efforts, including their clinical studies for CLR 131.

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Cellectar Biosciences (NASDAQ: CLRB) announced a public offering of common stock, raising approximately $24.5 million at $1.35 per share. The offering is registered under Form S-3, effective since August 20, 2020. Concurrently, a private placement of Series D convertible preferred stock is expected to generate about $20.5 million. Each share of preferred stock is convertible into shares of common stock, pending stockholder approval. Both transactions are set to close around December 28, 2020. Proceeds will support the company’s cancer treatment initiatives.

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FAQ

What is the current stock price of Cellectar Biosciences (CLRB)?

The current stock price of Cellectar Biosciences (CLRB) is $0.318 as of March 7, 2025.

What is the market cap of Cellectar Biosciences (CLRB)?

The market cap of Cellectar Biosciences (CLRB) is approximately 14.1M.

What is Cellectar Biosciences' core technology?

Cellectar Biosciences utilizes its proprietary Phospholipid Drug Conjugate (PDC) platform to deliver therapeutic payloads directly to cancer cells, enhancing efficacy and minimizing off-target effects.

What is iopofosine I 131?

Iopofosine I 131 is Cellectar's lead asset, a small-molecule PDC that uses iodine-131 to target and destroy cancer cells. It is under clinical evaluation for multiple cancer indications.

What types of cancers does Cellectar target?

Cellectar focuses on both hematologic malignancies, such as multiple myeloma and Waldenstrom’s macroglobulinemia, and solid tumors, including pancreatic, triple-negative breast, and colorectal cancers.

How does Cellectar differentiate itself from competitors?

Cellectar’s proprietary PDC platform enables precise targeting of cancer cells, reducing off-target effects and improving safety. Its focus on radiopharmaceuticals and orphan drug markets further differentiates it.

What are the key challenges Cellectar faces?

Cellectar faces challenges such as regulatory hurdles, isotope supply chain complexities, and the high capital requirements typical of clinical-stage biopharmaceutical companies.

What is CLR 121225?

CLR 121225 is an actinium-225-based radioconjugate targeting solid tumors. It leverages alpha-emitting isotopes for precision therapy in cancers with significant unmet needs.

What is the significance of the PDC platform?

The PDC platform enables targeted delivery of diverse therapeutic payloads to cancer cells, improving efficacy and safety. It supports both internal drug development and external collaborations.

What regulatory designations has Cellectar received?

Cellectar’s lead asset, iopofosine I 131, has received Orphan Drug and Fast Track Designations from the U.S. FDA for various indications, highlighting its potential in addressing unmet medical needs.
Cellectar Biosciences Inc

Nasdaq:CLRB

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14.12M
45.32M
2.84%
34.55%
4.52%
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