Full Press Release Details
Cellectar Biosciences Announces Results
of NCI-Sponsored Study of CLR 125 Showing
Potential Effect Against Triple Negative Breast Cancer
MADISON, Wis., June 23, 2016 (GLOBE NEWSWIRE) -- Cellectar Biosciences,
Inc. (Nasdaq: CLRB) ("the company"), an oncology-focused biotechnology company, today announces the results of the first
phase of a National Cancer Institute (NCI)-funded Small Business Innovation Research (SBIR) Phase 1 contract for a study of CLR
125, a radiotherapeutic isotope, which may be uniquely suited to treat micro-metastatic disease, conjugated to the company's
proprietary phospholipid drug conjugate (PDC) delivery platform.
The study demonstrated that a single dose of CLR 125 reduced
the volume of human-derived primary triple negative breast cancer xenografts (tumor models) by approximately 60 percent, compared
to a control vehicle (p<0.001), as well as significantly extending survival. CLR 125 also significantly weakened the progression
of micrometastases (p< 0.01) and reduced established metastases (p< 0.01) compared to the control vehicle. Importantly, within
96 hours of dosing, investigators observed that radioactivity cleared from subjects' blood and organs and accumulated primarily
in the tumor cells where it was retained past 144 hours.
"These study results provide further validation of the
benefits of our Phospholipid Drug Conjugate (PDC) development program, whether in cytotoxics, as in our previously announced paclitaxel
program or radiotherapeutics, as this study demonstrated," said Jim Caruso, president and CEO of Cellectar Biosciences. "Further,
these data clearly show that our PDC delivery platform may possess clinical utility in a broad range of cancer types with a wide
variety of cytotoxic compounds."
This trial represents the first phase of the SBIR contract for
a Phase 1 study sponsored by NCI. Following a complete review of the data, an assessment of potential clinical applications, and
differentiated product benefits, both NCI and the company will determine whether to advance CLR 125 into phase 2 of the contract.
About Cellectar Biosciences, Inc.
Cellectar Biosciences is developing phospholipid drug conjugates (PDCs) designed to provide cancer targeted delivery of diverse
oncologic payloads to a broad range of cancers and cancer stem cells. Cellectar's PDC Delivery Platform is based on the company's
proprietary phospholipid ether analogs. These novel small-molecules have demonstrated highly selective uptake and retention in
a broad range of cancers. Cellectar's PDC pipeline includes product candidates for cancer therapy and cancer diagnostic imaging.
The company's lead therapeutic PDC, CLR 131, utilizes iodine-131, a cytotoxic radioisotope, as its payload. CLR 131 is currently
being evaluated under an orphan drug designated Phase 1 study in patients with relapsed or refractory multiple myeloma. The company
is actively developing PDCs for targeted delivery of chemotherapeutics such as paclitaxel (CLR 1602-PTX), a preclinical stage
product candidate, and plans to expand its PDC chemotherapeutic pipeline through both in-house and collaborative R&D efforts.
For additional information please visit www.cellectarbiosciences.com
This 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, 2015. These forward-looking statements are made only as of the date
hereof, and we disclaim any obligation to update any such forward-looking statements.