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GLP study marks a key milestone in Autonomix's path to achieve regulatory approvals
Company remains on track to submit Investigational Device Exemption ("IDE"), and if approved, commence U.S. clinical trials in 2026 to support a De Novo FDA application
Autonomix Medical, Inc. (NASDAQ: AMIX) ("Autonomix" or the "Company"), a medical device company dedicated to advancing precision nerve-targeted treatments, today announced that it has commenced a Good Laboratory Practice (GLP) preclinical study required by the FDA at CBSET, a state-of-the-art pre-clinical translational research institute, for its Sensing and RF Ablation System as a treatment for pancreatic cancer pain.
Posted In: AMIX