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Clinical Trial Summary

KAE609 will be evaluated primarily for hepatic safety of single and multiple doses in sequential cohorts with increasing doses.This study aims to determine the maximum safe dose of the investigational drug KAE609 in malaria patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03334747
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date November 16, 2017
Completion date November 23, 2019

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