Full Press Release Details
Cellectar Reports Financial
Results for First Quarter 2022 and Provides a Corporate Update
PARK, N.J., May 10, 2022 -- Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage clinical biopharmaceutical
company focused on the discovery, development and commercialization of targeted drugs for the treatment of cancer, today announced financial
results for the first quarter ended March 31, 2022 and provided a corporate update.
Recent Corporate Highlights
agreement of the independent DMC that the pre-specified futility analysis for our pivotal Phase 2b trial of iopofosine I-131 in WM
was achieved represents an important milestone," said James Caruso, president and CEO of Cellectar. "We look forward to continuing
iopofosine's clinical development and remain appreciative of the strong support by the patient advocacy groups, community clinicians
and WM academic thought leadership as we collectively partner to treat this orphan designated cancer. In multiple myeloma, we continue
to enrich our CLOVER-1 trial and are optimistic that iopofosine I-131 will help to address an unmet medical need in this indication."
Financial Highlights
About Cellectar Biosciences, Inc.
Cellectar Biosciences
is focused on the discovery and development of drugs for the treatment of cancer. The company is developing proprietary drugs 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 PDCs that specifically target cancer cells to deliver improved efficacy and better
safety as a result of fewer off-target effects. The company's PDC platform possesses the potential for the discovery and development
of the next-generation of cancer-targeting treatments, and it plans to develop PDCs independently and through research and development
The company's product
pipeline includes iopofosine, a small-molecule PDC designed to provide targeted delivery of iodine-131 (radioisotope), proprietary preclinical
PDC chemotherapeutic programs and multiple partnered PDC assets. The company is currently investigating iopofosine in a global, open-label,
pivotal expansion cohort in relapsed or refractory WM patients who have received at least two prior lines of therapy, including those
who have failed or had a suboptimal response to Bruton tyrosine kinase inhibitors. The WM cohort will enroll up to 50 patients to evaluate
the efficacy and safety of iopofosine for marketing approval. The company is also evaluating iopofosine in highly refractory multiple
myeloma patients in its Phase 2 CLOVER-1 study and relapsed/refractory pediatric cancer patients with sarcomas or brain tumors in the
Phase 1 CLOVER-2 study.
The Phase 1 pediatric
study is an open-label, sequential-group, dose-escalation study to evaluate the safety and tolerability of iopofosine in children and
adolescents with relapsed or refractory cancers, including malignant brain tumors, neuroblastoma, sarcomas, and lymphomas (including Hodgkin's
lymphoma). The Phase 1 study is being conducted internationally at seven leading pediatric cancer centers.
more information, please visit www.cellectar.com and www.wmclinicaltrial.com or join the conversation by liking
and following us on the company's social media channels: Twitter, LinkedIn, and Facebook.
Forward-Looking Statement
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 including our expectations of the impact of the COVID-19 pandemic. 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 disruptions at our sole source supplier of iopofosine,
the ability to attract and retain partners for our technologies, the identification of lead compounds, the successful preclinical development
thereof, patient enrollment and the completion of clinical studies, the FDA review process and other government regulation, our ability
to maintain orphan drug designation in the United States for iopofosine, 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, 2021, and
our Form 10-Q for the quarter ended March 31, 2022, when filed. These forward-looking statements are made only as of the date
hereof, and we disclaim any obligation to update any such forward-looking statements.
+++ TABLES TO FOLLOW +++
CELLECTAR BIOSCIENCES, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
| March 31, | ||||||||
| 2022 | December 31, | |||||||
| (Unaudited) | 2021 | |||||||
| ASSETS | ||||||||
| CURRENT ASSETS: | ||||||||
| Cash and cash equivalents | $ | 30,634,122 | $ | 35,703,975 | ||||
| Prepaid expenses and other current assets | 760,420 | 867,485 | ||||||
| Total current assets | 31,394,542 | 36,571,460 | ||||||
| Fixed assets, net | 331,144 | 344,491 | ||||||
| Right-of-use asset, net | 183,286 | 204,644 | ||||||
| Long-term and other assets | 81,214 | 81,214 | ||||||
| TOTAL ASSETS | $ | 31,990,186 | $ | 37,201,809 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| CURRENT LIABILITIES: | ||||||||
| Accounts payable and accrued liabilities | $ | 4,511,716 | $ | 3,854,914 | ||||
| Lease liability | 139,594 | 135,449 | ||||||
| Total current liabilities | 4,651,310 | 3,990,363 | ||||||
| Long-term lease liability, net of current portion | 129,714 | 166,292 | ||||||
| TOTAL LIABILITIES | 4,781,024 | 4,156,655 | ||||||
| COMMITMENTS AND CONTINGENCIES (Note 7) | ||||||||
| STOCKHOLDERS' EQUITY: | ||||||||
| Preferred stock, $0.00001 par value; 7,000 shares authorized; Series D preferred stock: 111 issued and outstanding as of March 31, 2022 and December 31, 2021 | 1,382,023 | 1,382,023 | ||||||
| Common stock, $0.00001 par value; 160,000,000 shares authorized as of March 31, 2022 and December 31, 2021; 61,101,251 and 61,101,263 shares issued and outstanding as of March 31, 2022 and December 31, 2021, respectively | 611 | 611 | ||||||
| Additional paid-in capital | 182,864,114 | 182,560,309 | ||||||
| Accumulated deficit | (157,037,586 | ) | (150,897,789 | ) | ||||
| Total stockholders' equity | 27,209,162 | 33,045,154 | ||||||
| TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY | $ | 31,990,186 | $ | 37,201,809 |
CELLECTAR BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
| Three Months Ended March 31, | ||||||||
| 2022 | 2021 | |||||||
| COSTS AND EXPENSES: | ||||||||
| Research and development | $ | 3,887,039 | $ | 4,633,194 | ||||
| General and administrative | 2,253,188 | 1,726,338 | ||||||
| Total costs and expenses | 6,140,227 | 6,359,532 | ||||||
| LOSS FROM OPERATIONS | (6,140,227 | ) | (6,359,532 | ) | ||||
| OTHER INCOME: | ||||||||
| Interest income, net | 430 | 2,362 | ||||||
| Total other income, net | 430 | 2,362 | ||||||
| NET LOSS | $ | (6,139,797 | ) | $ | (6,357,170 | ) | ||
| BASIC AND DILUTED NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS PER COMMON SHARE | $ | (0.10 | ) | $ | (0.13 | ) | ||
| SHARES USED IN COMPUTING BASIC AND DILUTED NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS PER COMMON SHARE | 61,101,262 | 48,139,189 |