This document presents a study on using the liquisolid technique to enhance the dissolution profile of the poorly water soluble drug lornoxicam. The objectives were to formulate liquisolid compacts of lornoxicam using different vehicles, carrier ratios, and coating materials to improve its solubility and dissolution rate compared to conventional tablets. Various tests were performed to characterize the liquisolid formulations and determine optimal formulation parameters. The results demonstrated that liquisolid compacts with certain vehicles and powder substrate ratios achieved complete drug release within 10 minutes, representing a significant enhancement over conventional tablets.