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Clinical Trial Summary

This is a Phase 1, randomized, double-blind, placebo-controlled, single ascending dose and multiple ascending dose study of ECC4703 in healthy volunteers and participants with treatment unnecessary LDL-C under 160 mg/dL


Clinical Trial Description

This study will be conducted in two cohorts of Single Ascending Dose (SAD) with a dose range from 1mg to 400mg and in four cohorts of Multiple Ascending Dose (MAD) with a dose range of 40mg to 160mg to Investigate the Safety, Tolerability, PK, and PD of ECC4703 in Healthy Volunteers and Participants with Treatment Unnecessary LDL-C under 160 mg/dL ;


Study Design


Related Conditions & MeSH terms

  • Fatty Liver
  • Non-alcoholic Fatty Liver Disease
  • Non-alcoholic Steatohepatitis (NASH)

NCT number NCT05552274
Study type Interventional
Source Eccogene
Contact Eccogene Clinical Trials
Phone 86-21-61053022
Email contact@eccogene.com
Status Recruiting
Phase Early Phase 1
Start date August 16, 2022
Completion date July 5, 2023

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