MedMira Inc. announced today that it received a Notice of Allowance from the United States Patent and Trademark Office for its rapid flow-through test (RFT) methodology, the technology platform its rapid tests are built on.
This patent protects the core innovation behind MedMira's fully commercialized line of rapid tests. The test can be used as an aid to diagnose one or multiple diseases using one test device and a single drop of blood. The Company's rapid tests have performed exceptionally well in rigorous clinical trials, earning regulatory approvals in major international markets including the United States, Canada, China, India, and the European Union. In a recent study led by Dr. S. M. Owen and published in the May 2008 issue of the Journal of Clinical Microbiology, MedMira's rapid HIV had the highest sensitivity and specificity of the FDA approved rapid tests assessed in the study. Additional results in the same study demonstrated that MedMira's rapid HIV detected early infection better than the other rapid tests and closely matched the performance of much more complex enzyme tests. MedMira is now poised to capitalize on its intellectual property estate in North American and the European Union through its partnership development strategy and program.