QSAM Biosciences Reports Second Quarter 2022 Financial Results and Provides Corporate Update
QSAM Biosciences Inc. reported progress in its Phase 1 clinical trial of CycloSam® for metastatic bone cancer. Preliminary results from the first patient show promising safety and efficacy signals. The company had a 57% decrease in net loss, reporting $1.33 million for the quarter ended June 30, 2022, down from $3.07 million in the same period last year. Operating expenses also decreased to $1.26 million compared to $2.90 million. The company plans to add clinical and reactor sites in Q3 2022 and aims for a NASDAQ uplisting in early 2023 if market conditions improve.
- 57% decrease in net loss to $1.33 million from $3.07 million year-over-year.
- Operating expenses reduced to $1.26 million from $2.90 million year-over-year.
- Initial results from the Phase 1 trial of CycloSam® suggest promising safety and efficacy.
- Plans to expand clinical trial and nuclear reactor sites in Q3 2022.
- Cash reserves decreased to $0.43 million, raising concerns about operational sustainability.
- Net loss attributable to common stockholders remains significant at $1.33 million.
Progress Shown in Phase 1 Clinical Program Evaluating CycloSam® Radiopharmaceutical Drug Candidate for Treatment of Metastatic Bone Cancer
AUSTIN, Texas, Aug. 16, 2022 (GLOBE NEWSWIRE) -- QSAM Biosciences Inc. (OTCQB: QSAM), a company developing next-generation therapeutic radiopharmaceuticals, including Samarium-153-DOTMP (CycloSam®), for the treatment of bone cancer and related diseases, today announces financial results for the second quarter ended June 30, 2022, as filed with the SEC on August 15, 2022 in the Company’s Form 10-Q, and provides a corporate update.
Recent Corporate Highlights:
- Initial, preliminary evaluation of the first patient dosed in Phase 1 clinical trial for CycloSam® for the treatment of metastatic bone cancer suggests promising results.
- Second patient dosing and completion of the first cohort of patients in the trial is expected in the third calendar quarter.
- Additional clinical trial sites for CycloSam® and additional nuclear reactor sites expected to be added in the third calendar quarter.
- Third key patent received in the United States covering the production and delivery of CycloSam®, strengthening Company’s extensive patent portfolio.
“We are encouraged by the initial, preliminary data from the first patient dosed with CycloSam®. While it is too early for formal conclusions to be made of these early results, we did see positive signals in terms of safety and efficacy. CycloSam performed how we expected it to perform, even given the lowest dosage in our dose-escalating study. Over the next few months, we expect to make steady progress in our first clinical trial, including establishing additional trial sites that will help us treat more patients, and qualifying additional nuclear reactors to build redundancy and efficiencies in our supply chain,” stated Douglas R. Baum, CEO and co-founder of the Company.
“Our decision to postpone our planned equity raise and NASDAQ uplisting in May was based on market conditions at that time. We are now seeing the beginnings of a turn-around in the broader biotech markets. If these continue, and we achieve the progress we expect in our clinical trials over the next six months, we intend to revisit the uplisting process in early 2023. We are actively working towards creating shareholder value in conjunction with our most important mission to help adult and pediatric patients suffering from bone cancer,” added Baum.
Summary Financial Results for the Quarter Ended June 30, 2022:
(All numbers except shares are approximated)
Net loss attributable to common stockholders for the quarter ended June 30, 2022, was
Operating expenses were
As of June 30, 2022, the Company had cash of approximately
As of June 30, 2022, the Company had 1,686,587 common shares outstanding. The Company did not issue any shares or options in the quarter. At the end of the second quarter of 2022 there were approximately 497,594 shares of common stock that could be issued upon the conversion of preferred stock, warrants and convertible debt, excluding employee stock options.
The following tables summarize our results of operations for the periods indicated, and are qualified in their entirety by the Company’s Form 10-Q for the period ended June 30, 2022, filed with the SEC on August 15, 2022, including the financial footnotes contained therein:
QSAM BIOSCIENCES, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
| June 30, | December 31, | |||||||
| 2022 | 2021 | |||||||
| (Unaudited) | ||||||||
| ASSETS | ||||||||
| CURRENT ASSETS | ||||||||
| Cash | $ | 429,353 | $ | 1,499,866 | ||||
| Prepaid expenses and other current assets | 108,221 | 135,014 | ||||||
| Deferred offering costs | - | 35,000 | ||||||
| TOTAL CURRENT ASSETS | 537,574 | 1,669,880 | ||||||
| TOTAL ASSETS | $ | 537,574 | $ | 1,669,880 | ||||
| LIABILITIES AND STOCKHOLDERS’ DEFICIT | ||||||||
| CURRENT LIABILITIES | ||||||||
| Accounts payable and accrued expenses | $ | 994,464 | $ | 569,321 | ||||
| Accrued payroll and related expenses | 588,805 | 95,400 | ||||||
| Accrued Series B preferred stock dividends | 228,584 | 153,343 | ||||||
| Convertible notes payable, net of discount | 550,550 | 532,400 | ||||||
| Notes payable - related parties | 7,500 | 7,500 | ||||||
| Debentures | - | 35,000 | ||||||
| TOTAL CURRENT LIABILITIES | 2,369,903 | 1,392,964 | ||||||
| TOTAL LIABILITIES | 2,369,903 | 1,392,964 | ||||||
| Redeemable convertible preferred stock - Series A; | 706,800 | 693,580 | ||||||
| STOCKHOLDERS’ DEFICIT | ||||||||
| Preferred stock, Series B, | 2 | 2 | ||||||
| Preferred stock, Series E-1, | - | - | ||||||
| Common stock, | 169 | 165 | ||||||
| Unearned deferred compensation | (472,292 | ) | (900,742 | ) | ||||
| Additional paid-in capital | 30,327,583 | 29,765,585 | ||||||
| Accumulated deficit | (32,394,591 | ) | (29,281,674 | ) | ||||
| TOTAL STOCKHOLDERS’ DEFICIT | (2,539,129 | ) | (416,664 | ) | ||||
| TOTAL LIABILITIES AND STOCKHOLDERS’ DEFICIT | $ | 537,574 | $ | 1,669,880 | ||||
QSAM BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
| For the three months ended | For the six months ended | |||||||||||||||
| June 30, | June 30, | |||||||||||||||
| 2022 | 2021 | 2022 | 2021 | |||||||||||||
| REVENUES | $ | - | $ | - | $ | - | $ | - | ||||||||
| OPERATING EXPENSES | ||||||||||||||||
| Payroll and related expenses | 791,721 | 2,552,199 | 1,548,120 | 5,015,020 | ||||||||||||
| Professional fees | 218,006 | 151,858 | 857,411 | 954,686 | ||||||||||||
| General and administrative | 49,300 | 51,794 | 168,768 | 46,048 | ||||||||||||
| Research and development expenses | 204,216 | 147,453 | 459,053 | 221,407 | ||||||||||||
| Total Operating Expenses | 1,263,243 | 2,903,304 | 3,033,352 | 6,237,161 | ||||||||||||
| LOSS FROM OPERATIONS | (1,263,243 | ) | (2,903,304 | ) | (3,033,352 | ) | (6,237,161 | ) | ||||||||
| OTHER INCOME (EXPENSE) | ||||||||||||||||
| Financing costs including interest | (20,203 | ) | (899 | ) | (38,340 | ) | (38,528 | ) | ||||||||
| Gain on sale of equity method investment | - | - | - | 100,000 | ||||||||||||
| Loss on debentures and accrued expenses converted to common stock | - | - | - | (390,068 | ) | |||||||||||
| Loss on conversion of bridge notes and accrued interest | - | - | - | (744,505 | ) | |||||||||||
| Total Other Expense, net | (20,203 | ) | (899 | ) | (38,340 | ) | (1,073,101 | ) | ||||||||
| Loss from operations before income taxes | (1,283,446 | ) | (2,904,203 | ) | (3,071,692 | ) | (7,310,262 | ) | ||||||||
| INCOME TAXES | - | - | - | - | ||||||||||||
| NET LOSS | (1,283,446 | ) | (2,904,203 | ) | (3,071,692 | ) | (7,310,262 | ) | ||||||||
| PREFERRED STOCK | ||||||||||||||||
| Series A preferred contractual dividends | (6,018 | ) | (162,819 | ) | (13,220 | ) | (170,717 | ) | ||||||||
| Series B preferred contractual dividends | (38,035 | ) | - | (75,241 | ) | - | ||||||||||
| Deemed dividend on conversion of Series A preferred stock to shares of common stock | - | - | - | (542,500 | ) | |||||||||||
| Deemed dividend on warrant modification | - | - | (41,225 | ) | - | |||||||||||
| NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS | $ | (1,327,499 | ) | $ | (3,067,022 | ) | $ | (3,201,378 | ) | $ | (8,023,479 | ) | ||||
| NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS: BASIC AND DILUTED: | $ | (0.79 | ) | $ | (4.42 | ) | $ | (1.91 | ) | $ | (12.72 | ) | ||||
| WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING: BASIC AND DILUTED | 1,677,681 | 693,323 | 1,677,681 | 630,645 | ||||||||||||
QSAM BIOSCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS
(UNAUDITED)
| For the six months ended June 30, | ||||||||
| 2022 | 2021 | |||||||
| CASH FLOWS FROM OPERATING ACTIVITIES | ||||||||
| Net Loss | $ | (3,071,692 | ) | $ | (7,310,262 | ) | ||
| Adjustments to reconcile net loss to net cash used in operations: | ||||||||
| Common stock issued for services | 254,751 | 693,566 | ||||||
| Stock-based compensation to employees and directors | 747,937 | 4,825,472 | ||||||
| Loss on conversion of bridge notes and accrued interest | - | 744,505 | ||||||
| Loss on conversion of debentures and accrued expense to common stock | - | 390,068 | ||||||
| Paid-in-kind interest - convertible bridge notes | - | 35,983 | ||||||
| Amortization of debt discount | 18,150 | - | ||||||
| Changes in operating assets and liabilities | ||||||||
| Decrease (increase) in prepaid expenses and other current assets | 26,793 | (12,621 | ) | |||||
| (Decrease) increase in accounts payable and accrued expenses | 425,143 | (69,366 | ) | |||||
| Increase in accrued payroll and related expenses | 493,405 | - | ||||||
| Net cash used in operating activities | (1,105,513 | ) | (702,655 | ) | ||||
| CASH FLOWS FROM FINANCING ACTIVITIES | ||||||||
| Repayments on promissory notes – related parties | - | (33,492 | ) | |||||
| Deferred offering costs | 35,000 | - | ||||||
| Proceeds for the issuance of preferred stock – Series B | - | 2,221,000 | ||||||
| Net cash provided by financing activities | 35,000 | 2,187,508 | ||||||
| NET INCREASE (DECREASE) IN CASH | (1,070,513 | ) | 1,484,853 | |||||
| CASH - Beginning of period | 1,499,866 | 8,304 | ||||||
| CASH - End of period | $ | 429,353 | $ | 1,493,157 | ||||
| SUPPLEMENTAL CASH FLOW DISCLOSURES: | ||||||||
| Payment of interest in cash | $ | - | $ | - | ||||
| Payment of income taxes | $ | - | $ | - | ||||
| NON-CASH INVESTING AND FINANCING ACTIVITIES: | ||||||||
| Accrual of contractual and deemed dividends on Series A convertible preferred stock | $ | 13,220 | $ | 557,577 | ||||
| Accrual of contractual dividends on Series B convertible preferred stock | $ | 75,241 | $ | - | ||||
| Deemed dividend on warrant modifications | $ | 41,225 | $ | - | ||||
| Conversion of convertible bridge notes and accrued interest to 165,692 shares of common stock | $ | - | $ | 3,633,983 | ||||
| Conversion of debentures and accrued expenses to common stock | $ | - | $ | 125,000 | ||||
| Conversion of Series A preferred stock to common stock | $ | - | $ | 120,000 | ||||
| Conversion of notes payable with related parties to Series B preferred stock and warrants | $ | - | $ | 23,000 | ||||
About QSAM Biosciences
QSAM Biosciences, Inc. is developing next-generation nuclear medicines for the treatment of cancer and related diseases. QSAM’s initial technology, CycloSam® (Samarium-153 DOTMP), is a clinical-stage bone targeting radiopharmaceutical developed by IsoTherapeutics Group LLC, pioneers in the nuclear medicine space who also have developed other FDA-approved radiopharmaceutical products. QSAM is led by an experienced executive team and Board of Directors that have completed numerous FDA approvals and multiple successful biotech exits.
CycloSam® has demonstrated preliminary safety and efficacy in animal studies and a single patient FDA-cleared human trial performed in 2020 at the Cleveland Clinic. This nuclear technology uses low specific activity Samarium-153 (resulting in far less undesirable europium impurity) and DOTMP, a chelator which targets sites of high mineral turnover (bone) and is believed to reduce or eliminate off-target migration making it, in management’s opinion, an ideal agent to treat primary and secondary bone cancers. Since CycloSam® delivers targeted radiation selectively to the skeletal system, it is also believed to be an important candidate for use in bone marrow ablation as pre-conditioning for bone marrow transplantation, and in procedures to reduce external beam radiation to bone tumors. This multi-patented drug candidate utilizes a radioisotope previously approved by the FDA, combined with a novel targeting chelant that has demonstrated preliminary increased efficacy and decreased side effects in animal models and veterinary treatment of bone cancer in dogs. Further, CycloSam® utilizes a streamlined, just-in-time manufacturing process that is well established.
Legal Notice Regarding Forward-Looking Statements: This news release contains "Forward-looking Statements." These statements relate to future events or our future financial performance. These statements are only predictions and may differ materially from actual future results or events. We disclaim any intention or obligation to revise any forward-looking statements whether as a result of new information, future developments or otherwise. There are important risk factors that could cause actual results to differ from those contained in forward-looking statements, including, but not limited to our ability to fully commercialize our technology, risks associated with changes in general economic and business conditions, regulatory risks, clinical trial risks, early stage versus late stage product safety and efficacy, actions of our competitors, the extent to which we are able to develop new products and markets, supply chain risks, the time and expense involved in such development activities, the ability to secure additional financing, the ability to consummate acquisitions and ultimately integrate them, the level of demand and market acceptance of our products, and changes in our business strategies. This is not an offering of securities and securities may not be offered or sold absent registration or an applicable exemption from the registration requirements.
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FAQ
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