Cellectar Granted U.S. Patent for the Treatment of Various Cancers and Cancer Stem Cells with CLR 131
June 07 2018 - 7:30AM
Cellectar Biosciences, Inc. (Nasdaq:CLRB), a clinical-stage
biopharmaceutical company focused on the discovery, development and
commercialization of targeted treatments for cancer, announces that
the U.S. Patent and Trademark Office (USPTO) has granted patent
application number 15/099,977 titled, “Ether and Alkyl Phospholipid
Compounds for Treating Cancer and Imaging Detection of Cancer Stem
Cells.” This new patent enhances the coverage for the use of CLR
131 as a treatment for multiple cancers including gliomas, lung
cancer, squamous cell carcinoma, renal cancer, melanoma, colorectal
cancer, ovarian cancer, prostate cancer, breast cancer, and
pancreatic cancer including cancer stem cells.
“This patent expands protection for our PDC compounds across a
number of significant cancers and importantly cancer stem cells.
The ability of our PDC pipeline products, including CLR 131, to
target both cancer cells and cancer stem cells for difficult to
treat tumors could provide improved therapeutic benefits,” stated
Jim Caruso, chief executive officer of Cellectar Biosciences. “The
patent also provides further coverage for CLR 131’s use in
underserved pediatric diseases such as glioma, an indication that
we plan to advance into the clinic in the second half of this
year.”
About Phospholipid Drug Conjugates™Cellectar's
product candidates are built upon a patented delivery and retention
platform that utilizes optimized PDCs to target cancer cells. The
PDC platform selectively delivers diverse oncologic payloads to
cancerous cells and cancer stem cells, including hematologic
cancers and solid tumors. This selective delivery allows the
payloads’ therapeutic window to be modified, which may maintain or
enhance drug potency while reducing the number and severity of
adverse events. This platform takes advantage of a metabolic
pathway utilized by all tumor cell types in all cell cycle stages.
Compared with other targeted delivery platforms, the PDC platform’s
mechanism of entry does not rely upon specific cell surface
epitopes or antigens. In addition, PDCs can be conjugated to
molecules in numerous ways, thereby increasing the types of
molecules selectively delivered. Cellectar believes the PDC
platform holds potential for the discovery and development of the
next generation of cancer-targeting agents.
About CLR 131CLR 131 is Cellectar’s
investigational radioiodinated PDC therapy that exploits the
tumor-targeting properties of the company's proprietary
phospholipid ether (PLE) and PLE analogs to selectively deliver
radiation to malignant tumor cells, thus minimizing radiation
exposure to normal tissues. CLR 131, is in a Phase 2 clinical study
in relapsed or refractory (R/R) MM and a range of B-cell
malignancies and a Phase 1 clinical study in patients with (R/R) MM
exploring fractionated dosing. In 2018 the company plans to
initiate a Phase 1 study with CLR 131 in pediatric solid tumors and
lymphoma, and a second Phase 1 study in combination with external
beam radiation for head and neck cancer.
About Cellectar Biosciences, Inc.Cellectar
Biosciences is focused on the discovery, development and
commercialization of drugs for the treatment of cancer. The company
plans to develop proprietary drugs independently and through
research and development (R&D) collaborations. The core drug
development strategy is to leverage our PDC platform to develop
therapeutics that specifically target treatment to cancer cells.
Through R&D collaborations, the company’s strategy is to
generate near-term capital, supplement internal resources, gain
access to novel molecules or payloads, accelerate product candidate
development and broaden our proprietary and partnered product
pipelines.
The company's lead PDC therapeutic, CLR 131, is in a Phase 1
clinical study in patients with relapsed or refractory (R/R) MM and
a Phase 2 clinical study in R/R MM and a range of B-cell
malignancies. In the second half of 2018 the company plans to
initiate a Phase 1 study with CLR 131 in pediatric solid tumors and
lymphoma, and a second Phase 1 study in combination with external
beam radiation for head and neck cancer. The company’s product
pipeline also includes two preclinical PDC chemotherapeutic
programs (CLR 1700 and 1900) and partnered assets include PDCs from
multiple R&D collaborations.
For more information please visit www.cellectar.com.
Forward-Looking Statement DisclaimerThis news
release contains forward-looking statements. You can identify these
statements by our use of words such as "may," "expect," "believe,"
"anticipate," "intend," "could," "estimate," "continue," "plans,"
or their negatives or cognates. These statements are only estimates
and predictions and are subject to known and unknown risks and
uncertainties that may cause actual future experience and results
to differ materially from the statements made. These statements are
based on our current beliefs and expectations as to such future
outcomes. Drug discovery and development involve a high degree of
risk. Factors that might cause such a material difference include,
among others, uncertainties related to the ability to raise
additional capital, uncertainties related to the ability to attract
and retain partners for our technologies, the identification of
lead compounds, the successful preclinical development thereof, the
completion of clinical trials, the FDA review process and other
government regulation, the volatile market for priority review
vouchers, our pharmaceutical collaborators' ability to successfully
develop and commercialize drug candidates, competition from other
pharmaceutical companies, product pricing and third-party
reimbursement. A complete description of risks and uncertainties
related to our business is contained in our periodic reports filed
with the Securities and Exchange Commission including our Form 10-K
for the year ended December 31, 2017. These forward-looking
statements are made only as of the date hereof, and we disclaim any
obligation to update any such forward-looking statements.
CONTACT: LHA Investor RelationsMiriam Weber
Miller212-838-3777mmiller@lhai.com
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