Vectus Biosystems Limited (Vectus or the Company) announced that the first cohort consisting of eight subjects has completed all protocol requirements for the 2mg dose in the Single Ascending Dose (SAD) component of its Phase I/IB trial entitled: The results for this cohort have been reviewed by the trial safety committee and it has been deemed safe to proceed with the next dosage level. The trial is registered on the Clinical Trials Protocol Registration and Results Systems (ClinicalTrials.gov) and has been provided with the identifier NCT04925050.