Qualigen Therapeutics Announces US FDA IND Clearance To Initiate Phase 1 Clinical Trial Of QN-302 For Treatment Of Advanced Or Metastatic Solid Tumors
Portfolio Pulse from Benzinga Newsdesk
Qualigen Therapeutics has received US FDA IND clearance to initiate Phase 1 clinical trial of QN-302 for the treatment of advanced or metastatic solid tumors. This clearance transitions Qualigen from a preclinical to a clinical-stage company and demonstrates its leadership in G4-targeting therapies for areas of high unmet need in oncology.
August 01, 2023 | 1:22 pm
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Qualigen Therapeutics' FDA IND clearance for Phase 1 clinical trial of QN-302 could potentially boost its stock as it transitions from a preclinical to a clinical-stage company.
The FDA IND clearance is a significant milestone for Qualigen Therapeutics as it allows the company to transition from preclinical to clinical-stage. This could potentially attract more investors, leading to a rise in the company's stock price.
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