Cellectar Biosciences to Report Full Year Financial Results and Host a Conference Call on Thursday, March 13, 2025
March 05 2025 - 7:05AM
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 the company will report financial results for the
full year ended December 31, 2024, and provide a corporate update
on March 13, 2025, at 8:30 a.m. Eastern Time.
Conference
Call & Webcast Details: |
Date: |
Thursday, March 13, 2025 |
Time: |
8:30 am Eastern Time |
Toll Free: |
1-800-717-1738 |
Conference
ID:Webcast: |
25759Click HERE |
A replay of the call 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.
Investor Contact:
Anne Marie Fields212-362-1200Precision AQ (formerly Stern
IR)annemariefields@precisionaq.com
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