Todos Medical Reports Second Quarter 2021 Financial Results
Todos Medical reported a positive net income of $3.39 million or $0.01 per share for Q2 2021, with revenue soaring to $1.7 million from $32,000 a year prior. The acquisition of Provista Diagnostics enhances the company’s capabilities in breast cancer testing and COVID-19 diagnostics. A Phase 2 clinical trial for its antiviral, Tollovir, is underway, with expectations to expand into India. The company received FDA approval for a new Tollovid regimen, bolstering its market presence. It aims for improved financial health and potential uplisting to a national exchange.
- Net income of $3.39 million for Q2 2021, up from a net loss of $2.58 million in Q2 2020.
- Total revenue increased to $1.7 million from $32,000 year-over-year.
- Acquisition of Provista Diagnostics strengthens breast cancer screening capabilities, with market potential estimated in billions.
- Phase 2 clinical trial for Tollovir underway, with plans for expansion into India.
- FDA approval for new 5-day Tollovid dosing regimen enhances market readiness.
- Operating loss of $1.66 million in Q2 2021, despite improved financial conditions.
- Cash decreased to $308,000 from $935,000 since December 2020.
Company recorded positive earnings of
New York, NY, and Tel Aviv, ISRAEL, Sept. 24, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Todos Medical, Ltd. (“Todos Medical”) (OTCQB: TOMDF), a comprehensive medical diagnostics and related solutions company, announced financial results today for the second quarter of 2021 ended June 30, 2021.
Corporate Highlights
Acquired Provista Diagnostics and Its Proprietary Videssa Breast Cancer Blood Test
Provista is a medical diagnostics company based in Alpharetta, Georgia that owns the intellectual property rights to the proprietary breast cancer blood test, Videssa®, and has a CLIA/CAP diagnostic testing laboratory currently performing COVID-19 PCR testing, primarily for the medical and entertainment industries. Todos Medical has begun ramping up Provista’s automated testing capacity as well as expanding its testing capabilities to include COVID variant testing and neutralizing antibody testing. When at full capacity the lab has automation in place to do up to 20,000 PCR tests, over 1,500 cPass neutralizing antibody tests, and 5,000 variant tests on a daily basis.
Videssa was developed to provide physicians with actionable information regarding breast cancer risk in women following an inconclusive mammogram result (BI-RADS III or IV), which primarily occurs in women with dense breasts. The results provided by the test have demonstrated specificity of
Launched Phase 2 Clinical Trial of Its Antiviral 3CL Protease Inhibitor NLC-V-01 (Tollovir™) in Hospitalized COVID-19 Patients
The trial is being conducted at Shaare Zedek Medical Center in Jerusalem, Israel to evaluate the safety and efficacy of Tollovir for the treatment of COVID-19 in hospitalized patients. Tollovir is a patent-pending therapeutic agent being developed through a joint venture between Todos Medical and NLC Pharma. 3CL protease inhibitors are targeted as desirable candidates for development of antiviral therapies against SARS-CoV-2 (the virus that causes COVID-19). Todos expects to provided interim data and to expand the study into India in the fourth quarter of 2021.
Receives FDA Certificate of Free Sale for New 5-Day Tollovid® Dosing Regimen
The US Food & Drug Administration granted the Company a new Certificate of Free Sale for a second dosing regimen for Tollovid™ as a dietary supplement. Under the new Certificate of Free Sale, the Company is authorized to market Tollovid with a dosing regimen of 60 pills over a five-day period, equivalent to 12 pills per day. Tollovid, a potent 3CL protease inhibitor botanical product, is a dietary supplement that helps to support and maintain healthy immune function.
Received Notice of Allowance from European Patent Office for Patent Application Covering Diagnosis of Cancer Using Proprietary Artificial Intelligence TBIA Immune Profiling Platform
The patent application specifically covers methods for capturing consistent data from infrared spectroscopy readers, as well as the application of various artificial intelligence algorithm development methods to the data. The ability of TBIA to make a diagnosis of cancer has first been applied to the detection of breast and colon cancers, where Todos Medical has received CE Marks in Europe paving the way for commercialization initially focused on TMB-2 (dense breast / inconclusive mammogram secondary screening) and TMB-1 (general breast cancer screening) cancer detection tests.
"We made significant strides in the second quarter to position Todos for future growth on several fronts, including receiving
Financial Highlights for Q2 2021
Revenues: Total revenue in the second quarter of 2021 was
Loss from Operations: The Company recorded an operating loss of
Net Income: The Company recorded net income of
Select Balance Sheet Items: The Company had cash of
"While we achieved significant business milestones in the second quarter, we also witnessed several key improvements to our financial condition as well," said Daniel Hirsch, CFO of Todos Medical. "Our asset base was expanded significantly through our acquisition of Provista while our deficit decreased by
About Todos Medical Ltd.
Founded in Rehovot, Israel with offices in New York City, Todos Medical Ltd. (OTCQB: TOMDF) engineers life-saving diagnostic solutions for the early detection of a variety of cancers. In 20201, Todos completed the acquisition of U.S.-based medical diagnostics company Provista Diagnostics, Inc. to gain rights to its Alpharetta, Georgia-based CLIA/CAP certified lab currently performing PCR COVID testing and Provista's proprietary commercial-stage Videssa® breast cancer blood test. The Company's state-of-the-art and patented Todos Biochemical Infrared Analyses (TBIA) is a proprietary cancer-screening technology using peripheral blood analysis that deploys deep examination into cancer's influence on the immune system, looking for biochemical changes in blood mononuclear cells and plasma. Todos' two internally-developed cancer-screening tests, TMB-1 and TMB-2, have received a CE mark in Europe. Todos is focused on the commercialization of Videssa and will bring the TBIA tests to market thereafter.
Todos has entered into a joint venture with NLC Pharma targeting diagnostic and testing solutions to address the COVID-19 pandemic. The Joint-Venture is pursuing the development of diagnostic tests targeting the 3CL protease, as well as 3CL protease inhibitors that target a fundamental reproductive mechanism of coronaviruses. The Company’s proprietary therapeutic candidate Tollovir™ is currently in a Phase 2 clinical trial to treat hospitalized COVID-19 patients in Israel, and is preparing to initiate Phase 2/3 clinical trials for both hospitalized and non-hospitalized patients in Israel.
Todos is also developing blood tests for the early detection of neurodegenerative disorders, such as Alzheimer's disease. The Lymphocyte Proliferation Test (LymPro Test™) is a diagnostic blood test that determines the ability of peripheral blood lymphocytes (PBLs) and monocytes to withstand an exogenous mitogenic stimulation that induces them to enter the cell cycle. It is believed that certain diseases, most notably Alzheimer's disease, are the result of compromised cellular machinery that leads to aberrant cell cycle re-entry by neurons, which then leads to apoptosis. LymPro is unique in the use of peripheral blood lymphocytes as a surrogate for neuronal cell function, suggesting a common relationship between PBLs and neurons in the brain.
Todos is also distributing certain (COVID-19) testing materials and supplies to CLIA-certified labs in the United States. The products cover multiple suppliers of PCR testing kits, extraction kits, automation materials and supplies, as well as COVID-19 antibody and antigen testing kits.
For more information, please visit https://www.todosmedical.com/.
Forward-looking Statements
Certain statements contained in this press release may constitute forward-looking statements. For example, forward-looking statements are used when discussing our expected clinical development programs and clinical trials. These forward-looking statements are based only on current expectations of management, and are subject to significant risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements, including the risks and uncertainties related to the progress, timing, cost, and results of clinical trials and product development programs; difficulties or delays in obtaining regulatory approval or patent protection for product candidates; competition from other biotechnology companies; and our ability to obtain additional funding required to conduct our research, development and commercialization activities. In addition, the following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: changes in technology and market requirements; delays or obstacles in launching our clinical trials; changes in legislation; inability to timely develop and introduce new technologies, products and applications; lack of validation of our technology as we progress further and lack of acceptance of our methods by the scientific community; inability to retain or attract key employees whose knowledge is essential to the development of our products; unforeseen scientific difficulties that may develop with our process; greater cost of final product than anticipated; loss of market share and pressure on pricing resulting from competition; and laboratory results that do not translate to equally good results in real settings, all of which could cause the actual results or performance to differ materially from those contemplated in such forward-looking statements. Except as otherwise required by law, Todos Medical does not undertake any obligation to publicly release any revisions to these forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. For a more detailed description of the risks and uncertainties affecting Todos Medical, please refer to its reports filed from time to time with the U.S. Securities and Exchange Commission.
Todos Corporate and Investor Contact:
Richard Galterio
Todos Medical
732-642-7770
rich.g@todosmedical.com
TODOS MEDICAL LTD.
CONDENSED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands except share and per share amounts)
Six months period ended June 30, | Three months period ended June 30, | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
Unaudited | Unaudited | |||||||||||||||
Revenues | $ | 6,763 | $ | 32 | $ | 1,732 | $ | 32 | ||||||||
Cost of revenues | (4,148 | ) | (11 | ) | (913 | ) | (11 | ) | ||||||||
Gross profit | 2,615 | 21 | 819 | 21 | ||||||||||||
Research and development expenses | (643 | ) | (569 | ) | (239 | ) | (465 | ) | ||||||||
Sales and marketing expenses | (1,958 | ) | (1,430 | ) | (599 | ) | (680 | ) | ||||||||
General and administrative expenses | (3,204 | ) | (925 | ) | (1,643 | ) | (595 | ) | ||||||||
Operating loss | (3,190 | ) | (2,903 | ) | (1,662 | ) | (1,719 | ) | ||||||||
Financing income (expenses), net | (10,485 | ) | (4,320 | ) | 5,171 | (866 | ) | |||||||||
Share in losses of affiliated companies accounted for under equity method, net | (492 | ) | - | (119 | ) | - | ||||||||||
Net income (loss) | $ | (14,167 | ) | $ | (7,223 | ) | $ | 3,390 | $ | (2,585 | ) | |||||
Basic and diluted net income (loss) per share | $ | (0.02 | ) | $ | (0.04 | ) | $ | 0.01 | $ | (0.01 | ) | |||||
Weighted average number of ordinary shares outstanding attributable to ordinary shareholders used in computation of basic and diluted net income (loss) per share | 585,225,006 | 164,423,927 | 575,898,572 | 189,945,607 |
CONDENSED CONSOLIDATED BALANCE SHEETSTODOS MEDICAL LTD.
(U.S. dollars in thousands except share and per share amounts)
As of | As of | |||||||
June 30, 2021 | December 31, 2020 | |||||||
Unaudited | ||||||||
ASSETS | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 308 | $ | 935 | ||||
Trade receivables | 1,792 | 378 | ||||||
Inventories | 1,704 | 536 | ||||||
Other current assets | 123 | 601 | ||||||
Total current assets | 3,927 | 2,450 | ||||||
Non-current assets: | ||||||||
Investment in affiliated companies accounted for under equity method, net | 658 | 745 | ||||||
Investment in other company | 455 | 224 | ||||||
Property and equipment, net | 2,596 | 1,999 | ||||||
Prepaid expenses | 361 | 591 | ||||||
Goodwill | 7,761 | - | ||||||
Intangible assets | 1,500 | - | ||||||
Total non-current assets | 13,331 | 3,559 | ||||||
Total assets | $ | 17,258 | $ | 6,009 | ||||
LIABILITIES AND SHAREHOLDERS’ DEFICIT | ||||||||
Current liabilities: | ||||||||
Receivables financing facility, net | $ | - | $ | 1,306 | ||||
Loans, net | 2,756 | 1,672 | ||||||
Accounts payable | 1,087 | 1,640 | ||||||
Deferred revenues | 13 | 844 | ||||||
Other current liabilities | 3,941 | 2,316 | ||||||
Liability for minimum royalties | 296 | 291 | ||||||
Total current liabilities | 8,093 | 8,069 | ||||||
Non-current liabilities: | ||||||||
Convertible bridge loans, net | 15,560 | 5,965 | ||||||
Derivative warrants liability, net | 7 | 301 | ||||||
Fair value of bifurcated convertible feature of convertible bridge loans | 2,077 | 2,500 | ||||||
Deferred taxes | 315 | - | ||||||
Liability for minimum royalties | 205 | 185 | ||||||
Total non-current liabilities | 18,164 | 8,951 | ||||||
Shareholders’ deficit: | ||||||||
Ordinary Shares of NIS 0.01 par value each: Authorized: 1,000,000,000 shares at June 30, 2021 and December 31, 2020; Issued and outstanding: 607,760,492 shares and 376,335,802 shares at June 30, 2021 and December 31, 2020, respectively | 1,765 | 1,059 | ||||||
Additional paid-in capital | 50,684 | 35,211 | ||||||
Accumulated deficit | (61,448 | ) | (47,281 | ) | ||||
Total shareholders’ deficit | (8,999 | ) | (11,011 | ) | ||||
Total liabilities and shareholders’ deficit | $ | 17,258 | $ | 6,009 |
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