Welcome to our dedicated page for Qualigen Therapeutics news (Ticker: QLGN), a resource for investors and traders seeking the latest updates and insights on Qualigen Therapeutics stock.
Qualigen Therapeutics, Inc. (symbol: QLGN) is an early-clinical-stage therapeutics company dedicated to the development of innovative treatments for both adult and pediatric cancer. Headquartered in Carlsbad, California, the company's core focus lies in its pioneering research to tackle malignant diseases through its advanced therapeutic programs.
Core Business:
Qualigen's primary business activity revolves around its two key therapeutic programs. The flagship program, QN-302, is an investigational small molecule that acts as a G-quadruplexes (G4)-selective transcription inhibitor. This molecule exhibits a strong binding affinity to G4 structures prevalent in cancer cells, making it a potent candidate in cancer therapy. Additionally, Qualigen has another promising preclinical therapeutic program in its pipeline.
Recent Achievements:
- Recently, Qualigen transitioned from a preclinical to a clinical-stage company following the Investigational New Drug (IND) clearance for QN-302. This milestone marks a significant progression in clinical development and potential cancer treatment breakthroughs.
- The company also divested its FastPack® diagnostics business for approximately $5 million in an all-cash transaction. This strategic move enables Qualigen to concentrate resources on advancing its therapeutics pipeline.
Current Projects:
The ongoing development of QN-302 is a testament to Qualigen's commitment to pioneering cancer treatment solutions. The company is actively engaged in early-phase clinical trials to validate the efficacy and safety of QN-302 and other pipeline candidates.
Financial Condition:
The financial stability of Qualigen is bolstered by the sale proceeds from the divested diagnostics business, providing the necessary capital to fund ongoing and future therapeutic projects. Continuous investments in research and development underscore the company's dedication to discovering and developing novel cancer therapies.
Partnerships:
Qualigen collaborates with various research institutions and industry leaders to advance its drug development initiatives. These partnerships are crucial for fostering innovation and expediting the therapeutic development process.
For more information about Qualigen Therapeutics, Inc., please visit www.qlgntx.com.
Qualigen Therapeutics (Nasdaq: QLGN) has initiated Good Laboratory Practice (GLP) toxicology studies for its lead oncology program QN-302, a transcription inhibitor targeting G4-expressing solid tumors like pancreatic cancer. Conducted by WuXi AppTec, these studies are essential for the IND submission expected in H1 2023. Successful completion will allow QN-302 to progress to human clinical trials, addressing a critical need in cancer therapy. The Company emphasizes its commitment to patient's safety and advancement of effective treatments amidst the challenges in cancer care.
Qualigen Therapeutics has promoted Benedict M. Abugan to Vice President, Head of Diagnostics and Corporate Communications, effective January 23, 2023. Mr. Abugan boasts over two decades of experience in the medical diagnostics field and has played a significant role in the commercialization of various Qualigen FastPack® products. His leadership roles have spanned investor relations, marketing, and technical support. CEO Michael Poirier expressed confidence in Mr. Abugan's future contributions, highlighting the company's aim to enhance its diagnostics business.
Qualigen focuses on developing cancer treatments and has an established diagnostics business.
Qualigen Therapeutics announced that the FDA has granted Orphan Drug Designation (ODD) to its lead drug candidate QN-302 for treating pancreatic cancer. This designation provides several advantages, including seven-year marketing exclusivity and potential tax credits. In 2019, approximately 89,248 people in the U.S. were estimated to have pancreatic cancer, qualifying it for ODD.
Qualigen aims to submit an IND application in the first half of 2023 for a Phase I clinical trial. The company is focused on developing treatments for rare cancers and maintaining its diagnostic products.
Qualigen Therapeutics (Nasdaq: QLGN) provided an update on its subsidiary, NanoSynex, highlighting progress made in 2022 and objectives for 2023. Key achievements include a majority investment transaction, development of a rapid Antimicrobial Susceptibility Test (AST), and successful pilot studies. Looking ahead, NanoSynex aims to secure CE approval, ISO certification, and conduct final clinical studies for the AST, which could significantly enhance infectious disease diagnostics, potentially saving lives and reducing healthcare costs.
Qualigen Therapeutics, Inc. has announced that it has regained compliance with Nasdaq's minimum bid price requirement. The company received notice from Nasdaq confirming that its common stock has maintained a closing bid price of at least $1.00 per share for 10 consecutive business days. This compliance resolves previous concerns related to its listing on The Nasdaq Capital Market. Qualigen focuses on developing cancer treatments and diagnostics, with investigational compounds like QN-302 and QN-247 targeted at various cancers.
Qualigen Therapeutics (Nasdaq: QLGN) has announced that it received FDA feedback following a pre-Investigational New Drug interaction for its QN-302 compound, aimed at treating advanced solid tumors. This guidance will aid in the preparation of their IND application, expected to be submitted in the first half of 2023. CEO Michael Poirier emphasized the importance of FDA input and collaboration with their Scientific Advisory Board as they advance QN-302 towards clinical trials.
Qualigen Therapeutics, Inc. (Nasdaq: QLGN) announced a 1-for-10 reverse stock split effective November 23, 2022. This decision aims to help the company regain compliance with Nasdaq's $1.00 minimum bid price requirement. The split was approved by stockholders at a reconvened annual meeting on October 28, 2022. Each 10 shares will convert to 1, and no fractional shares will be issued, though cash will be paid for any fractions. This move is deemed crucial for securing the company’s listing on Nasdaq and advancing its cancer therapeutic programs.
Qualigen Therapeutics, Inc. (Nasdaq: QLGN) reported a 25% year-over-year increase in sales of its FastPack diagnostics for Q3 2022, totaling $1.4 million. The company's net loss was approximately $4.1 million, consistent with the prior year. R&D costs decreased to $1.7 million as the company shifts focus from COVID-19 to its core therapeutics pipeline. Significant progress was noted in preclinical data for QN-302 and QN-247. Shareholders approved a reverse stock split to comply with Nasdaq listing requirements. Cash reserves stand at $6.6 million, expected to fund operations through Q3 2023.
Qualigen Therapeutics, Inc. (Nasdaq: QLGN) presented preclinical data on its RAS-targeted platform at the Fourth RAS Initiative Symposium held from October 17-19, 2022. The company is focused on developing treatments for cancers driven by RAS oncogenes. Two key posters highlighted the efficacy of its lead candidate, RAS-F, which demonstrated the potential to inhibit tumor growth in malignant peripheral nerve sheath tumors and pancreatic cancer. Qualigen aims to address the unmet need for more effective RAS-targeted therapies, as current options are limited.
Qualigen Therapeutics, Inc. (Nasdaq: QLGN) announced that President Amy Broidrick and Chief Medical Officer Tariq Arshad, MD, will present a corporate overview at the LD Micro Main Event XV from October 25-27, 2022. The presentation is scheduled for October 26 at 12:30 PM PT. Attendees can view the livestream by registering online. Qualigen focuses on developing treatments for adult and pediatric cancers and offers diagnostic solutions. Their investigational compounds, including QN-302 and QN-247, aim to inhibit cancer cell proliferation.
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