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Voyageur Pharmaceuticals Advances Frances Creek Project, Paving the Way for a Secure, Vertically Integrated Barium Contrast Product Line
NewMediaWire · The Newswire

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CALGARY, ALBERTA - March 4, 2025 (NEWMEDIAWIRE) - Voyageur Pharmaceuticals Ltd. (TSX.V:VM) (OTC Pink:VYYRF) ("Voyageur" or the "Company") is pleased to announce the commencement of the Frances Creek barium contrast media project, powered by a $600,000 grant from Alberta Innovates. With $350,000 in funding already released, Voyageur has commenced processing the high-grade Frances Creek ore samples, to produce natural, high-purity pharmaceutical grade barium sulfate, which will serve as the primary Active Pharmaceutical Ingredient (API) in Voyageur's barium contrast media product development program.

The Alberta Innovates grant funding accelerates a transformative clinical performance evaluation, benchmarking the natural Frances Creek barium contrast media against existing synthetic barium contrast media and iodinated contrast media solutions. This research aims to highlight the imaging quality using Frances Creek barium sulfate, thus reinforcing our market positioning and potentially driving future sales growth. The research focus is to test Voyageurs contrast media products using Frances Creek barium, in comparative studies in human test subjects, evaluating images from computed tomography (CT) and Fluoroscopy examinations.

Brent Willis, President, CEO, and Director of Voyageur, stated, "We are excited to start processing Frances Creek samples to develop our active pharmaceutical ingredient. This marks a key milestone in demonstrating the efficacy and economic viability of our Frances Creek barium contrast project. By producing Health Canada licensed barium contrast media with natural barium, Voyageur aims to offer cost-effective and high-quality product lines, to allow for a secure supply chain for the radiology market that is currently experiencing supply chain constraints."

Phase 1 Clinical Evaluation Update

Voyageur announced on January 13, 2025 (Testing) that the company commenced testing of its current barium contrast media formulations in human subjects, to ensure efficacy and safety in clinical settings. Following the reformulation of one barium contrast media product, to meet performance expectations, a production batch has been manufactured and is undergoing laboratory analysis. It is expected to be released within 2 weeks for final performance validation in clinics. With positive outcomes, Phase 1 testing is set for completion by the end of April. Four of the five barium contrast media products have already shown promising initial results. Once testing of the re-formulated fifth product is complete, the data will undergo thorough evaluation by our consulting teams and Scientific Advisory Board. Upon approval, the full product line will be cleared for market release in Canada.