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Clinical Trial Summary

This is a clinical study aiming to assess pharmacokinetics and biomarker evidence of ZE46-0134 efficacy in Healthy Volunteers after single and multiple daily doses of the study drug


Clinical Trial Description

This is a Phase 1, double-blind, placebo-controlled, dose escalation study to evaluate the safety, tolerability, PK, PD of orally administered ZE46-0134 in Healthy Volunteers. The study will be conducted in 2 parts: a single ascending dose (SAD) part at up to 5 dose levels and a multiple ascending dose (MAD) part at up to 3 dose levels. Evaluation of dose levels will be conducted in a sequential fashion with lower dose levels evaluated first in the sequence. Dosing in each cohort will start with two sentinel participants with one of the two sentinels randomised to receive ZE46-0134 and the other randomised to receive placebo. The food-effect will be investigated in SAD part and safety/PK of co-administration with rabeprazole will be investigated in MAD part. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06399315
Study type Interventional
Source Eilean Therapeutics
Contact Ekaterina Dokukina, MD, Mphil
Phone 069728309
Email kdokukina@eileanther.com
Status Recruiting
Phase Phase 1
Start date July 28, 2023
Completion date November 2024

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