Qualigen Therapeutics, Inc today announces that NanoSynex Ltd, a company with whom Qualigen recently entered into definitive agreements to acquire a majority stake, will be featured at BioMed Israel on May 11, 2022. BioMed Israel is being held at David InterContinental Hotel in Tel Aviv May 10-12, 2022.
Innovative Technology Aims to AccelerateAntimicrobial Susceptibility Test Result Times by Six-Fold
CARLSBAD, Calif., May 10, 2022 (GLOBE NEWSWIRE) -- Qualigen Therapeutics, Inc. (Nasdaq: QLGN), a diversified life sciences company focused on developing treatments for adult and pediatric cancers with potential for Orphan Drug Designation, while also commercializing diagnostics, today announces that NanoSynex Ltd, a company with whom Qualigen recently entered into definitive agreements to acquire a majority stake, will be featured at BioMed Israel on May 11, 2022. BioMed Israel is being held at David InterContinental Hotel in Tel Aviv May 10-12, 2022.
Michael Poirier, Qualigen’s Chairman and CEO, commented, “The prestigious opportunity provided to NanoSynex is based on their innovation and dedication to develop what we believe may become an industry-changing technology. This recognition supports Qualigen’s interest to invest in NanoSynex, and we are looking forward to collaborating with their formidable team to help develop and commercialize this potentially life-saving technology.”
NanoSynex’s innovative technology is an Antimicrobial Susceptibility Testing (AST) platform that aims to provide clinical laboratories worldwide with a rapid, accurate and personalized test for bacterial infections, with the goal of quickly matching the correct antibiotics to treat a patient’s particular infection. Antibiotic misuse and overuse have given rise to antibiotic resistant bacteria, commonly known as superbugs, which the World Health Organization has called one of the top ten global public health threats facing humanity. NanoSynex’s potentially game-changing AST platform aims to enable better targeting of antibiotics to ultimately result in faster and more efficacious treatment, hence reducing hospitals mortality and morbidity rates.
One of the highlights of the Biomed Israel 2022 Exhibition is the Start-Up Pavilion, dedicated to providing a highly respected platform for innovative companies to maximize exposure and partnering opportunities. Strategically located in the Israel Innovation Authority Pavilion, this integral space is a focal point for visits from local and overseas delegations and individuals, consisting of potential collaborators, partners, and investors.
“We are honored and privileged to be featured at Biomed Israel 2022, the foremost international life science conference in Israel. The Start-Up Pavilion provides the greatest opportunity to further our key partnerships, and to put a spotlight on the critical need to dramatically accelerate and personalize the diagnostic process through revolutionary AST,” added NanoSynex Co-Founder and Chief Executive Officer, Diane Abensur Bessin.
AboutQualigenTherapeutics,Inc.
Qualigen Therapeutics, Inc. is a diversified life sciences company focused on developing treatments for adult and pediatric cancer, as well as maintaining and expanding its core FDA-cleared FastPack® System, which has been used successfully in diagnostics for over 20 years. Our investigational QN-302 compound is a small molecule selective transcription inhibitor with strong binding affinity to G4s prevalent in cancer cells; such binding could, by stabilizing the G4s against “unwinding,” help inhibit cancer cell proliferation. Our investigational QN-247 compound inhibits nucleolin, a key multi-functional regulatory protein that is overexpressed in cancer cells; QN-247 may thereby be able to inhibit the cells’ proliferation. QN-247 has shown promise in preclinical studies for the treatment of acute myeloid leukemia (AML). The investigational compounds within Qualigen’s RAS-F family of RAS oncogene protein-protein interaction inhibitor small molecules are believed to inhibit or block the binding of mutated RAS genes’ proteins to their effector proteins, thereby leaving the proteins from the mutated RAS unable to cause further harm. In theory, such mechanism of action may be effective in the treatment of about one quarter of all cancers, including certain forms of pancreatic, colorectal, and lung cancers. In addition to its oncology drug pipeline, Qualigen has an established diagnostics business which manufactures and distributes proprietary and highly accurate rapid blood testing systems to physician offices and small hospitals for the management of prostate cancer and other diseases and health conditions.
For more information about Qualigen Therapeutics, Inc., please visit www.qualigeninc.com.
About NanoSynex
NanoSynex is a MedTech company that aims at providing new solutions to improve testing quality, patient outcomes, and reduce healthcare costs by speeding up diagnostic processes. NanoSynex is focused on the development and commercialization of a rapid innovative Antimicrobial Susceptibility Test (AST). The technology is based on a purely phenotypic approach and uses a microfluidic disposable test card platform and method that optimizes bacterial growth. This disruptive development was born from exciting research discoveries at the lab of Professor Shulamit Levenberg, former Dean of the Technion Institute of Technology – Biomedical Engineering Faculty.
For more information about NanoSynex, please visit www.nanosynex.com.
Forward-LookingStatements
This news release contains forward-looking statements by Qualigen that involve risks and uncertainties and reflect the Company’s judgment as of the date of this release. These statements include those related to the satisfaction of closing conditions in connection with the proposed transaction with NanoSynex and the Company’s prospects and strategy for its diagnostics business and development of its therapeutic drug candidates. Actual events or results may differ from the Company’s expectations. For example, there can be no assurance that the closing conditions for the NanoSynex transaction will be satisfied or that the Company will be able to maintain its diagnostic sales and marketing engine without interruption following the expiration of the distribution agreement with Sekisui Diagnostics, compete with others in this industry or expand market demand and/or market share for its diagnostics product, nor can there be any assurance that the Company will be able to successfully develop any drugs (including QN-302, QN-247 and RAS-F); that preclinical development of the Company’s drugs (including QN-302, QN-247 and RAS-F, and the deprioritized infectious-disease drug candidate QN-165) will be completed on any projected timeline or will be successful; that any clinical trials will be approved to begin by or will proceed as contemplated by any projected timeline, or at all; that any future clinical trial data will be favorable or that such trials will confirm any improvements over other products or lack negative impacts; that any drugs will receive required regulatory approvals (or Fast Track designation or Orphan Drug status) or that they will be commercially successful; that patents will issue on the Company’s owned and in-licensed patent applications; that such patents, if any, and the Company’s currently owned and in-licensed patents would prevent competition; or that the Company will be able to procure or earn sufficient working capital to complete the development, testing and launch of the Company’s prospective therapeutic products (including QN-302, QN-247 and RAS-F, and QN-165). The Company’s stock price could be harmed if any of the events or trends contemplated by the forward-looking statements fails to occur or is delayed or if any actual future event otherwise differs from expectations. Additional information concerning these and other risk factors affecting the Company’s business can be found in the Company’s prior filings with the Securities and Exchange Commission, including its most recent annual report on Form 10-K, all of which are available at www.sec.gov.
The Company disclaims any intent or obligation to update these forward-looking statements beyond the date of this news release, except as required by law. This caution is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.
Contact:
Jules Abraham
JQA Partners, Inc.
917-885-7378
jabraham@jqapartners.com
Source: Qualigen Therapeutics, Inc.
