Spectral Medical Announces Second Quarter and Provides Corporate Update

Core Insights - Spectral Medical Inc. reported significant clinical and operational progress in Q2 2025, particularly with the Tigris trial, which is pivotal for the PMA submission to the FDA [3][4][7] - The company achieved a revenue increase of 73% year-over-year for Q2 2025, driven by product sales and non-dilutive funding from Vantive [8][12] - Operating expenses decreased by 47% in Q2 2025 compared to the previous year, contributing to a reduced loss for the quarter [9][13] Clinical Development - The Tigris trial, a Phase III study evaluating PMX for endotoxic septic shock, completed patient enrollment in April 2025 and is on track to report topline results by mid-August 2025 [3][6] - The company has submitted all non-clinical studies to the FDA and plans to submit clinical results by the end of October 2025 [6][8] - The EDEN study, completed in Q4 2023, provided critical data on septic shock, indicating a significantly higher mortality rate for patients with endotoxic septic shock [6][11] Financial Performance - Revenue for Q2 2025 was $813,000, up from $471,000 in Q2 2024, marking a 73% increase [8] - Product revenue for Q2 2025 reached $403,000, an 86% increase from $217,000 in the same period last year [8] - Operating expenses for Q2 2025 were $2,514,000, down from $4,702,000 in Q2 2024, primarily due to finance income from a promissory note [9][10] Balance Sheet and Funding - The company ended Q2 2025 with cash of $3,100,000, a slight increase from $2,988,000 at the end of 2024 [15] - Spectral entered into a promissory note agreement with Vantive for up to $10 million, providing financial flexibility for regulatory processes and commercialization planning [5][12] - Total liabilities increased to $45,672,000 as of June 30, 2025, compared to $32,865,000 at the end of 2024 [21] Market Position and Product Development - PMX, the company's therapeutic hemoperfusion device, is already approved for use in Japan and Europe and has been used over 360,000 times [17] - The Tigris trial is designed as a 2:1 randomized study of 150 patients, utilizing Bayesian statistics to evaluate PMX's effectiveness [18] - The company is collaborating with Vantive on post-approval commercialization planning, aligning efforts with potential FDA approval timelines [6][12]