Qualigen Therapeutics reported a net loss of $3.5 million, or $0.69 per share, for the quarter ended June 30, 2023. The company divested its FastPack® diagnostics business for approximately $5 million and received FDA IND clearance for QN-302.
Received US FDA Investigational New Drug (IND) clearance to initiate a Phase 1 clinical trial for QN-302.
Divested FastPack® diagnostics business for approximately $5 million to support advancement of therapeutics pipeline.
Plans to initiate Phase 1 clinical trial for QN-302 in the second half of 2023.
Continue to advance compounds within Pan-RAS therapeutic platform and on track to identify a late in vivo stage candidate by the end of the year.
Qualigen is looking forward to initiating their Phase 1 clinical trial of QN-302 in the second half of this year and potentially providing a treatment option in the future to patients who have not responded to or have relapsed following treatment with available therapies.