TORONTO--(BUSINESS WIRE)--Antibe Therapeutics Inc. (“Antibe” or the “Corporation”) (TSXV:ATE; OTCQX:ATBPF) is pleased to report that the pre-scheduled single ascending dose portion of its Phase I program has been completed and has reached its primary objectives of safety and tolerability of ATB-346, up to the maximum dose tested (1500 mg). The results of this portion of the Phase I program have met the corporation’s expectations based on extensive pre-clinical studies, and support the continuation of the Phase I program into the multiple ascending dose and food-effect portions, both of which are underway and are expected to be completed by January 2015.
Help employers find you! Check out all the jobs and post your resume.
