Preclinical Data Highlighting Uptake and Enhanced Anti-Tumor Effects of Cellectar’s CLR 131 in Head and Neck Cancer Presen...
16 Avril 2018 - 2:00PM
Cellectar Biosciences (Nasdaq:CLRB), a clinical-stage
biopharmaceutical company focused on the discovery, development and
commercialization of drugs for the treatment of cancer, announces
the presentation of CLR 131 preclinical data in a poster discussion
entitled “Therapeutic Combination of Radiolabeled CLR1404 with
External Beam Radiation in Head and Neck Cancer Murine Xenograft
Models” at the American Association for Cancer Research (AACR)
Annual Meeting underway in Chicago. The discussion, hosted on
Sunday, April 15, 2018 was led by Chunrong Li, assistant scientist,
Department of Human Oncology, University of Wisconsin School of
Medicine and Public Health.
The purpose of the study was to evaluate the anti-tumor effect
of CLR 131 in combination with external beam radiation (XRT). The
results demonstrated uptake of CLR 131 across multiple head and
neck cancer (HNC) cell lines and xenograft models, and synergistic
anti-tumor effects when CLR 131 was combined with XRT. The
combination of CLR 131 and fractionated XRT showed enhanced tumor
growth inhibition compared with single modality treatment in the 6
HNC xenograft models. Importantly, the findings suggest potential
efficacy using CLR 131 combined with reduced-dose XRT in HNC
patients. High-dose XRT while effective for localized disease,
produces significant co-morbidities for patients, especially those
suffering from diffuse disease. The potential to reduce the XRT
dose may also result in decreased toxicity to normal tissue, a
common side effect of high-dose XRT.
As a key milestone of their Head and Neck SPORE Grant (NIH P50
DE026787), the University of Wisconsin-Madison is initiating the
first human clinical trial combining CLR 131 and external beam
radiation in patients with recurrent HNC in the second half of
2018. The costs associated with the Phase 1 study will be covered
in their entirety through the grant and the study represents a
fourth clinical trial using the company’s lead PDC, CLR 131.
“As we continue both preclinical and clinical evaluation of our
lead cancer targeting compound CLR 131, our potential to
meaningfully impact a broad range of cancers continues to grow,”
said James Caruso, chief executive officer of Cellectar
Biosciences. “We are encouraged by the data highlighted at AACR
showing enhanced receptivity to treatment and inhibition of tumor
growth, while potentially reducing toxicities associated with
current standard of care treatment.”
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 is CLR 131. The 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, 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, 2016. 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
Cellectar Biosciences (NASDAQ:CLRBW)
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