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Clinical Trial Summary

This is a first in human, randomized, double blind, SAD (with food effect) followed by a MAD study of Trichomylin® conducted in healthy adult participants.

Clinical Trial Description

The study is designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and food effect of Trichomylin® in healthy adult participants. Up to 56 participants will be enrolled into 1 of 4 SAD cohorts (8 per cohort) and 3 MAD cohorts (8 per cohort). Participants will undergo a Screening period between 21 days and 28 days prior to randomization/dose administration (for SAD and MAD respectively), admission to the clinical research unit (CRU), pre-dose assessment, post-dose assessment, and a final end of study (EOS)/follow-up or early termination (ET) visit (if applicable). ;

Study Design

Related Conditions & MeSH terms

NCT number NCT04867057
Study type Interventional
Source ZYUS Life Sciences Inc.
Contact Mahsa Abrishami, Dr
Phone +1 (306) 651-7734
Email [email protected]
Status Recruiting
Phase Phase 1
Start date April 29, 2021
Completion date February 10, 2022

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