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.
CONTACT: Jules Abraham JQA Partners 917-885-7378 jabraham@jqapartners.com INVESTOR CONTACT: Stephanie Prince Managing Director PCG Advisory Group 646-762-4518 sprince@pcgadvisory.com
