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Cellectar Biosciences to Present at the 37th Annual Roth Conference

Key Takeaway: Cellectar Biosciences, Inc. has announced that its management team will present at the 37th Annual Roth Conference on March 17, 2025. The presentation will provide an overview of the company's ongoing development and commercialization of cancer treatments, leveraging their proprietary Phospholipid Drug Conjugate platform. Cellectar's product pipeline includes promising assets with FDA designations, underscoring their potential in addressing significant unmet needs in cancer care.

Market Sentiment Analysis

POSITIVE FACTORS

  • Cellectar will present at the notable 37th Annual Roth Conference.
  • The company has a promising pipeline including drugs for several cancers.
  • iopofosine I 131 has received multiple FDA designations indicating potential.
  • The presentation may enhance visibility and interest in their innovative treatments.

Full Press Release Details

FLORHAM PARK, N.J., March 11, 2025 (GLOBE NEWSWIRE) -- 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, today announced that members of its management team will present an overview of the company at the upcoming 37th Annual Roth Conference. Details are as follows:
Date: Monday, March 17
Time: 8:30 AM Eastern Time
A replay of the corporate presentation will be available on the Events section of the company’s Investor Relations website.
About Cellectar Biosciences, Inc.
Cellectar Biosciences is a late-stage clinical biopharmaceutical company focused on the discovery and development of proprietary drugs for the treatment of cancer, independently and through research and development collaborations. The company’s core objective is to leverage its proprietary Phospholipid Drug Conjugate™ (PDC) delivery platform to develop the next-generation of cancer cell-targeting treatments, delivering improved efficacy and better safety as a result of fewer off-target effects.
The company’s product pipeline includes its lead assets: iopofosine I 131, a PDC designed to provide targeted delivery of iodine-131 (radioisotope); CLR 121225, an actinium-225 based program being targeted to several solid tumors with significant unmet need, such as pancreatic cancer; and CLR 121125, an iodine-125 Auger-emitting program targeted in other solid tumors, such as triple negative breast, lung and colorectal, as well as proprietary preclinical PDC chemotherapeutic programs and multiple partnered PDC assets.
In addition, iopofosine I 131 has been studied in Phase 2b trials for relapsed or refractory multiple myeloma (MM) and central nervous system (CNS) lymphoma, and the CLOVER-2 Phase 1b study, targeting pediatric patients with high-grade gliomas, for which Cellectar is eligible to receive a Pediatric Review Voucher from the FDA upon approval. The FDA has also granted iopofosine I 131 six Orphan Drug, four Rare Pediatric Drug and two Fast Track Designations for various cancer indications.
For more information, please visit www.cellectar.com or join the conversation by liking and following us on the company’s social media channels: Twitter, LinkedIn, and Facebook.

Frequently Asked Questions

When will Cellectar Biosciences present at the Roth Conference?

Cellectar Biosciences will present on March 17 at 8:30 AM Eastern Time.

What is the focus of Cellectar Biosciences?

Cellectar Biosciences focuses on discovering and developing cancer treatment drugs.

What is Cellectar's lead drug asset?

Cellectar's lead asset is iopofosine I 131, a targeted delivery treatment.

What designations has iopofosine I 131 received?

It has received six Orphan Drug and four Rare Pediatric Drug designations.

Where can I find more about Cellectar Biosciences?

Visit www.cellectar.com for more information on Cellectar Biosciences.

Last updated: Mar 11, 2025