Cosmo Pharmaceuticals N.V. announced topline results from a randomized, international, multi-center study evaluating the safety and efficacy of artificial intelligence (AI) device GI Genius(TM) as an aid for the detection of colorectal polyps in combination with colonoscopy. The DETECT study was designed to provide evidence of the advantages of using GI Genius(TM) in the real-time detection of colorectal polyps and to assess if the use of GI Genius(TM) would decrease the miss rates of colorectal polyps and adenomas when compared to white light endoscopy. The topline results show that both the primary and the secondary endpoint of the study were met with very high statistical significance: the adenoma miss rate (AMR) was significantly lower when GI Genius(TM) was used in the first colonoscopy as compared to when white light endoscopy was used in the first colonoscopy (15.5% vs 32.4%; p-value <0.001). The polyp miss rate (PMR) was significantly lower when GI Genius(TM) was used in the first colonoscopy as compared to when white light endoscopy was used in the first colonoscopy (16.9% vs 31.1%; p-value <0.001). These findings demonstrate that the use of GI Genius(TM) significantly decreases the miss rate of both adenomas and polyps, further confirming the enhancements GI Genius(TM) adds to colonoscopy procedures. The primary endpoint of the study was the adenoma miss rate (AMR), representing the percentage of adenomas or carcinomas that were found at the second colonoscopy and were therefore undetected at the first colonoscopy. The secondary endpoint of the study was the polyp miss rate (PMR), representing the percentage of polyps that were found at the second colonoscopy and were therefore undetected at the first colonoscopy. The objective of the study was to assess if the AMR and PMR were lower when GI Genius(TM) was used in the first colonoscopy, as compared to when white light endoscopy was used in the first colonoscopy. The DETECT study (clinicialtrials.gov identification number: NCT03954548) was conducted in the US and Europe (Italy and United Kingdom). Conducted in university hospitals and community clinics, study subject included male and female patients aged 45 or older undergoing a screening or surveillance colonoscopy for colorectal cancer. In total, 249 subjects were randomized in the study, of whom 229 subjects completed the study and were included in the primary efficacy analysis, undergoing two consecutive colonoscopies that were randomly assigned in order of which they were conducted: one with GI Genius(TM) and a colonoscopy with white light endoscopy. GI Genius(TM) is authorized in the US and approved in Europe; however, indications may differ.