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Clinical Trial Summary

The aim of this first-in-human study is to assess the safety, tolerability, PK and exploratory pharmacodynamics (PD) of single and multiple oral ascending doses of OMT-28 in healthy male subjects to support further clinical development of OMT-28 in the indication of atrial fibrillation (AF) and to obtain data on food and gender effects of OMT-28 to guide dosing for Phase II trials.


Clinical Trial Description

This first-in-human study will be carried out in one study center involving multiple steps. Up to 100 healthy male and female subjects will be enrolled. The study consists of 4 parts:

1. a single ascending dose (SAD) part

2. a multiple ascending dose (MAD) part

3. a single dose, double cross-over food effect (FE) part.

4. a single dose gender effect part (female subjects group) The safety and PK data will be evaluated by the DSMC after each cohort to decide on further dose escalation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03078738
Study type Interventional
Source Omeicos Therapeutics GmbH
Contact
Status Completed
Phase Phase 1
Start date February 8, 2017
Completion date March 12, 2018

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