Aspire Biopharma Holdings, Inc. (Nasdaq:ASBP) has announced the completion of patient dosing in its Phase 1 clinical trial of an oral transmucosal fast-acting high-dose aspirin formulation. The trial, conducted in the United States, aims to compare the pharmacokinetic and pharmacodynamic characteristics of the aspirin formulation in healthy volunteers. Topline results from the study are expected to be presented in the middle of the third quarter of 2025. The company plans to use these insights to further discussions with the FDA and to support potential partnership opportunities. Following the trial, Aspire intends to submit a section 505(b)(2) NDA for approval to market the high-dose aspirin product.
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