8-K
Cellectar Biosciences, Inc. (CLRB)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d)
OF THE SECURITIESEXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported): August 5, 2022
Cellectar Biosciences, Inc.
(Exact name of Registrant as Specified in itsCharter)
| Delaware | 1-36598 | 04-3321804 |
|---|---|---|
| (State or other jurisdiction<br><br> of incorporation) | (Commission <br><br>File Number) | (IRS Employer<br><br> Identification No.) |
100Campus Drive, Florham Park, NJ, 07932
(Address of principal executive offices) (ZipCode)
Registrant’s telephone number, including
area code: (608) 441-8120
N/A
(Former Name or Former Address, if ChangedSince Last Report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
| ¨ | Written communications pursuant to Rule 425 under the Securities<br>Act (17 CFR 230.425) |
|---|---|
| ¨ | Soliciting material pursuant to Rule 14a-12 under the Exchange<br>Act (17 CFR 240.14a-12) |
| --- | --- |
| ¨ | Pre-commencement communications pursuant to Rule 14d-2(b) under<br>the Exchange Act (17 CFR 240.14d-2(b)) |
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| ¨ | Pre-commencement communications pursuant to Rule 13e-4(c) under<br>the Exchange Act (17 CFR 240.13e-4(c)) |
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Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered |
|---|---|---|
| Common Stock, par value $0.00001 per share | CLRB | The Nasdaq Capital Market |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ¨
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨
| Item 2.02. | Results of Operations and Financial Condition |
|---|
On August 5, 2022, we issued a press release announcing our financial results for the three months and six months ended June 30, 2022. A copy of the press release is furnished as Exhibit 99.1 and is incorporated by reference herein.
| Item 9.01. | Financial Statements and Exhibits |
|---|---|
| (d) Exhibits<br><br>Number | Title |
| --- | --- |
| 99.1 | Press release dated August 5, 2022, entitled “Cellectar Reports Financial Results for Second Quarter 2022” |
| 104 | Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101) |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| CELLECTAR BIOSCIENCES, INC. | ||
|---|---|---|
| Date: August 5, 2022 | By: | /s/ Chad J. Kolean |
| Name: | Chad J. Kolean | |
| Title: | Chief Financial Officer |
Exhibit 99.1
Cellectar Reports FinancialResults for Second Quarter 2022
FLORHAMPARK, N.J., August 5, 2022 -- Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted treatments for cancer, today announced financial results for the second quarter ended June 30, 2022.
“During the second quarter, ipofosine passed an important milestone as an independent data monitoring committee completed a futility/efficacy assessment and unanimously recommended continuation of our pivotal Phase 2B trial in Waldenstrom’s macroglobulinemia (WM),” said James Caruso, president and CEO of Cellectar. “This global trial includes participation from leading institutions and world-renowned WM thought leadership, and we are excited by the active engagement of our investigators.” Mr. Caruso continued, “We also look forward to providing data from our phase 2a multiple myeloma trial and our phase 1 pediatric trial for malignant brain tumors and sarcomas in the second half of 2022.”
Second Quarter 2022Financial Highlights
| · | Cashand Cash Equivalents: As of June 30, 2022, the company had cash and cash equivalents of $24.8 million, compared<br>to $35.7 million as of December 31, 2021. Net cash used in operating activities during the six months ended June 30, 2022 was<br>approximately $10.8 million. The company believes its cash on hand is adequate to fund basic budgeted operations into the third quarter<br>of 2023. |
|---|---|
| · | Researchand Development Expense: R&D expense for the three months ended June 30, 2022 was approximately $4.5 million,<br>which was relatively consistent when compared to approximately $4.6 million for the three months ended June 30, 2021. For the six<br>months ended June 30, 2022, R&D expense was approximately $8.4 million, while the comparable period in 2021 was $9.3 million.<br>The reduction in the six month period was due primarily to the timing of activities related to our ongoing WM pivotal trial as trial<br>initiation costs were higher in the prior year. |
| --- | --- |
| · | Generaland Administrative Expense: G&A expense for the three months ended June 30, 2022 was $2.9 million, compared<br>to $1.4 million for the same period in 2021. G&A expense in the six months ended June 30, 2022 was approximately $5.2 million,<br>as compared to approximately $3.1 million in the prior year. These increases were driven largely by increased professional fees and personnel<br>costs. |
| --- | --- |
| · | NetLoss: The net loss attributable to common stockholders for the quarter ended June 30, 2022 was ($7.4) million, or<br>($1.22) per share, compared to ($6.0) million, or ($1.14) per share, in the quarter ended June 30, 2021, while the loss attributable<br>to common stockholders in the first half of 2022 was ($13.6) million, or ($2.22) per share, compared to ($12.4) million, or ($2.45) per<br>share for the first half of 2021. |
| --- | --- |
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 collaborations.
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.
For 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 StatementDisclaimer
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.
Contacts
Investors:
Monique Kosse
Managing Director
LifeSci Advisors
212-915-3820
monique@lifesciadvisors.com
+++ TABLES TO FOLLOW +++
CELLECTAR BIOSCIENCES, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited)
| December 31, | |||||
|---|---|---|---|---|---|
| 2021 | |||||
| ASSETS | |||||
| CURRENT ASSETS: | |||||
| Cash and cash equivalents | 24,805,565 | $ | 35,703,975 | ||
| Prepaid expenses and other current assets | 479,668 | 867,485 | |||
| Total current assets | 25,285,233 | 36,571,460 | |||
| Fixed assets, net | 364,838 | 344,491 | |||
| Right-of-use asset, net | 161,111 | 204,644 | |||
| Long-term and other assets | 81,214 | 81,214 | |||
| TOTAL ASSETS | 25,892,396 | $ | 37,201,809 | ||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | |||||
| CURRENT LIABILITIES: | |||||
| Accounts payable and accrued liabilities | 5,462,267 | $ | 3,854,914 | ||
| Lease liability | 143,843 | 135,449 | |||
| Total current liabilities | 5,606,110 | 3,990,363 | |||
| Long-term lease liability, net of current portion | 92,214 | 166,292 | |||
| TOTAL LIABILITIES | 5,698,324 | 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 June 30, 2022 and December 31, 2021 | 1,382,023 | 1,382,023 | |||
| Common stock, 0.00001 par value; 160,000,000 shares authorized as of June 30, 2022 and December 31, 2021; 6,110,123 and 6,110,125 shares issued and outstanding as of June 30, 2022 and December 31, 2021, respectively | 61 | 61 | |||
| Additional paid-in capital | 183,284,617 | 182,560,859 | |||
| Accumulated deficit | (164,472,629 | ) | (150,897,789 | ) | |
| Total stockholders’ equity | 20,194,072 | 33,045,154 | |||
| TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY | 25,892,396 | $ | 37,201,809 |
All values are in US Dollars.
CELLECTAR BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2022 | 2021 | 2022 | 2021 | |||||||||
| COSTS AND EXPENSES: | ||||||||||||
| Research and development | $ | 4,498,657 | $ | 4,627,636 | $ | 8,385,656 | $ | 9,260,830 | ||||
| General and administrative | 2,936,867 | 1,401,053 | 5,190,095 | 3,127,391 | ||||||||
| Total costs and expenses | 7,435,524 | 6,028,689 | 13,575,751 | 12,388,221 | ||||||||
| LOSS FROM OPERATIONS | (7,435,524 | ) | (6,028,689 | ) | (13,575,751 | ) | (12,388,221 | ) | ||||
| OTHER INCOME: | ||||||||||||
| Interest income, net | 481 | 659 | 911 | 3,021 | ||||||||
| Total other income | 481 | 659 | 911 | 3,021 | ||||||||
| NET LOSS | $ | (7,435,043 | ) | $ | (6,028,030 | ) | $ | (13,574,840 | ) | $ | (12,385,200 | ) |
| BASIC AND DILUTED NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS PER COMMON SHARE | $ | (1.22 | ) | $ | (1.14 | ) | $ | (2.22 | ) | $ | (2.45 | ) |
| SHARES USED IN COMPUTING BASIC AND DILUTED NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS PER COMMON SHARE | 6,110,124 | 5,276,380 | 6,110,125 | 5,046,427 |