Odyssey Health, Inc. Completes Safety Evaluation of Cohort II for Concussion Drug

Las Vegas, NV, June 29, 2022 (GLOBE NEWSWIRE) – Odyssey Health, Inc. (OTC Pink: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-saving medical products, today announced positive safety findings from Cohort II of their Phase I clinical trial. Odyssey’s trial involves administering PRV-002, the Company’s novel drug to treat concussion, to healthy human subjects. Data from Cohort II indicates that the drug was safe and well-tolerated.

The trial is being conducted at Nucleus Network, a leading clinical research organization. Cohort II was unblinded and evaluated by the Safety Review Committee. Cohort II included six healthy human volunteers who received one dose of PRV-002 or placebo followed by evaluations for abnormal responses. No severe adverse events were noted, as PRV-002 was well-tolerated. Vital signs, EKG readings, sleep patterns and breathing function were all normal.  Blood labs showed no alterations associated with the PRV-002 treatment. Pharmacokinetic analysis was done by comparing these results to the animal findings of max concentration (NOEL) prior to toxicity to determine the highest concentration (Cmax) of PRV-002 and the time course (AUC) of PRV-002 concentrations in the blood to ensure that elevating the dose would be safe.