Study to Evaluate the Influence of Tegoprazan on the Pharmacokinetics of

Clinical Trial Description

Evaluation criteria - Pharmacokinetic assessment with plasma concentrations of proguanil and cycloguanil - Safety assessments with adverse event monitoring including subjective/objective symptoms, physical examination, vital signs, electrocardiogram, and laboratory tests ;

Study Design

See also
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NCT number	NCT04568772
Study type	Interventional
Source	Seoul National University Hospital
Contact
Status	Completed
Phase	Phase 1
Start date	November 25, 2020
Completion date	August 3, 2021

Study to Evaluate the Influence of Tegoprazan on the Pharmacokinetics of Proguanil in Healthy Volunteers

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms