Medicure

Medicure presented the design, rationale and initial baseline data of the phase‑3 MEND‑PNPO study of the oral P5P formulation MC‑1 for treatment of the rare PNPO deficiency at the 16th European Epilepsy Congress. The open‑label, multicenter 52‑week study began in January 2023 and targets about 10 genetically confirmed patients aged two years and older; so far nine patients have been enrolled and three have completed the one‑year follow‑up. Starting doses ranged from 14 to 58 mg/kg/day, measured steady‑state P5P levels were 59.8–165 ng/ml, and MC‑1 is not yet approved by the FDA. Medicure also plans to present the study at upcoming professional congresses in Montreal and Denver. » Mais em de.investing.com

Medicure reported Q2 2026 net revenue of CAD 7.4 million (+10.4% vs. year‑ago), driven by ZYPITAMAG and its pharmacy network, which accounted for about 79.9% of revenue. Adjusted EBITDA improved to CAD 172,000, but the reported net loss widened to CAD 1.4 million, mainly due to a CMS-related rebate liability (CAD 864,000) and higher R&D spending for the Phase III MC-1 program. AGGRASTAT sales fell 61.1% on intensified generic competition, and cash declined to CAD 1.8 million. Management emphasizes a focus on further growth of ZYPITAMAG, integration of the pharmacies and progress on MC-1, but did not provide formal guidance. » Mais em de.investing.com

Medicure reports a 43.6% revenue increase in Q1 2026 to CAD 7.9 million and narrowed its net loss to CAD 406,000, or -0.04 CAD per share. Growth was driven mainly by ZYPITAMAG (revenue through insurance channels +150.3%) and pharmacy acquisitions, while AGGRASTAT declined 42.4% due to generic competition. Cash fell to CAD 1.5 million; the company forecasts revenues of CAD 25.06 million for 2026 and CAD 28.2 million for 2027 and is focusing on expanding its pharmacy business. » Mais em de.investing.com