Toronto, Ontario–(Newsfile Corp. – August 26, 2025) – Theralase® Technologies Inc. (TSXV: TLT) (OTCQB: TLTFF) (“Theralase®” or the “Company“), a clinical stage pharmaceutical pioneering light, radiation, sound and drug-activated therapeutics for the treatment of cancer, bacteria and viruses has released the Company’s unaudited condensed consolidated interim 2Q2025 financial statements (“Financial Statements“). Theralase® will be hosting a conference call on Wednesday, September 3rd at 11:00 am ET, which will include a presentation of the financial and operational results for the fiscal quarter ending June 30th, 2025. Questions are welcome. To ensure we have time to review and properly address them during the call, please send them in advance to mperraton@theralase.com. Zoom Meeting Link: https://us02web.zoom.us/j/87203480163Webinar ID: 872 0348 0163 Conference Call in: 1-647-558-0588 (Canada) / 1-646-558-8656 (US) – not required for those attending by Zoom An archived version will be available on the website following the conference call. Financial Summary:For the six-month period ended June 30th: To view an … Read More
Theralase® Extends Warrants
Theralase® Technologies Inc. plans to extend the expiry date of 4,800,000 share purchase warrants from June 30, 2025, to June 30, 2028. The warrants, issued in 2023, remain exercisable at $0.35 per share under the same terms. The extension is subject to TSX Venture Exchange approval. Theralase® develops light- and drug-activated therapies targeting cancer, bacteria, and viruses.
Theralase® Closes Non-Brokered Private Placement
Theralase® Technologies Inc. closed a $571,000 private placement, issuing 2,855,000 units at $0.20 each. Funds will support its Phase II bladder cancer trial, Rutherrin® development, and corporate needs. Each unit includes a share and a five-year warrant at $0.30. Insider participation totaled 669,700 units. The offering awaits TSX Venture Exchange approval.
Theralase® Completes Annual General and Special Meeting
Theralase® successfully completed its 2025 Annual General Meeting, sharing strategic plans for 2025–2026 focused on clinical advancements and commercialization. A recording of the presentation is available for shareholders.
Theralase® Annual General Meeting
Theralase® Technologies Inc. reminds shareholders of its Annual General and Special Meeting (AGSM) on June 11, 2025, at 4:30 pm ET in Toronto. Following the meeting, a virtual corporate presentation and Q&A session will be held at 5:15 pm ET via Zoom to discuss strategic objectives for 2025-2026. An archived recording will be available the next business day.
Theralase® 1Q2025 Financial Statements
Theralase® reported Q1 2025 results showing lower revenue and increased R&D expenses, ongoing Study II enrollment with promising bladder cancer interim data, continued HSV treatment development, and plans for Rutherrin® clinical trials starting early 2026 targeting multiple cancers.
CORRECTION FROM SOURCE: Theralase® to Present Groundbreaking Research at ASTRO 2025
Theralase® will present preclinical data comparing radiation-activated Rutherrin® versus radiation alone at ASTRO 2025, highlighting tumor targeting, immune activation, and survival benefits; clinical trials for various cancers begin early 2026.
Theralase® to Present Groundbreaking Research at ASTRO 2025
Theralase®’s Rutherrin® is 100x more effective than radiation alone in preclinical cancer models, showing tumor targeting, immune activation, and improved survival; Phase I/II clinical trials start early 2026 targeting multiple cancers.
Theralase® Provides Corporate Update
Theralase advances Ruvidar® trials for bladder and other cancers, targeting NDA submissions by 2026, launching multiple Phase I/II studies, seeking US listing, and pursuing international partnerships for commercialization and research collaboration.
Theralase® Clinical Data Presented at Canadian Bladder Cancer Forum and American Urological Association
Theralase® presented interim Phase II data showing Ruvidar™’s strong safety and efficacy in treating BCG-unresponsive bladder cancer, with durable complete responses, no serious drug-related adverse events, and potential for regulatory approval in 2026.