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TML-OSE-22 is a preclinical-stage, ready-to-use (RTU) injectable formulation of a proton-pump inhibitor (PPI), likely esomeprazole, developed by Themis Medicare. As part of Themis's focus on Novel Drug Delivery Systems (NDDS), this product is designed as a stable, pre-mixed solution for intravenous administration, eliminating the need for the manual reconstitution of lyophilized powder typically required for PPIs. This "ready-to-use" format is intended to streamline clinical workflows, reduce the risk of dosing errors, and minimize potential microbial contamination in hospital settings. The active ingredient functions by irreversibly inhibiting the H+/K+-ATPase enzyme system (the gastric acid pump) in the parietal cells of the stomach, thereby providing potent and long-lasting suppression of gastric acid secretion. TML-OSE-22 is being developed for conditions where rapid acid suppression is required and oral administration is not feasible, such as severe gastroesophageal reflux disease (GERD) and peptic ulcer disease.
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