Todos Medical, Ltd. today announced that its CEO Gerald Commissiong will be presenting a corporate overview at the Benzinga Global Small Cap Conference which is being held virtually on October 27-28, 2021.
New York, NY, and Tel Aviv, ISRAEL, Oct. 26, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Todos Medical Ltd. (“Todos Medical”) (OTCQB: TOMDF), a comprehensive medical diagnostics and related solutions company, today announced that its CEO Gerald Commissiong will be presenting a corporate overview at the Benzinga Global Small Cap Conference which is being held virtually on October 27-28, 2021. The event bridges the gap between small cap companies, investors and traders.
SESSION DETAILS
WHAT: October Small Cap Conference - Todos Medical
WHEN: 1:55 PM/ET - October 28
WHERE: FREE ticket at https://www.benzinga.com/events/small-cap/
“With the upcoming interim data read out expected this quarter from our ongoing Phase 2 clinical trial evaluating the safety and efficacy of Tollovir® in treating hospitalized COVID-19 patients currently ongoing in Israel, conducted together with our joint venture partners NLC Pharma, we are very excited about what the near-term future holds for Todos Medical,” said Gerald E. Commissiong, President & CEO of Todos Medical. “Tollovir is an Mpro (Main protease, 3CL protease or 3CLpro) inhibitor that has high binding affinity to the Mpro receptor, low cross reactivity with other receptors in the human body, as well as strong anti-cytokine activity that potentially makes it an ideal therapeutic candidate for the treatment of COVID-19 at all stages of disease from prevention to late-stage hospitalization. With the recent publication in Nature Neuroscience of key data identifying for the first time that Mpro is potentially the main driver of brain-related COVID-19 symptoms such as ‘Brain Fog’ and memory loss, and emerging evidence that Mpro downregulates immune responses to SARS-CoV-2 infection in the brain and elsewhere in peripheral vascular tissues that could potentially explain the diversity of immune response, we believe it is now becoming more important than ever to focus on the development of Tollovir as a potentially game-changing treatment for COVID-19 patients.”
For more information, please visit www.todosmedical.com. For more information on the Company’s CLIA/CAP certified lab Provista Diagnostics, Inc. please visit www.provistadx.com.
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 2021, 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