First in Man Clinical Trial of Emodepside (BAY 44-4400)
Completed
Bayer
Phase 1
This study will investigate the safety, tolerability, and pharmacokinetics of single
ascending doses of emodepside (BAY 44-4400) in healthy male volunteers. This study will also
conduct an exploratory investigation of the relative bioavailability of emodepside
administered as tablets and determine the effect of food on the pharmacokinetics.
First in Man Clinical Trial of Emodepside (BAY 44-4400)
Completed
Bill and Melinda Gates Foundation
Phase 1
This study will investigate the safety, tolerability, and pharmacokinetics of single
ascending doses of emodepside (BAY 44-4400) in healthy male volunteers. This study will also
conduct an exploratory investigation of the relative bioavailability of emodepside
administered as tablets and determine the effect of food on the pharmacokinetics.
First in Man Clinical Trial of Emodepside (BAY 44-4400)
Completed
Drugs for Neglected Diseases
Phase 1
This study will investigate the safety, tolerability, and pharmacokinetics of single
ascending doses of emodepside (BAY 44-4400) in healthy male volunteers. This study will also
conduct an exploratory investigation of the relative bioavailability of emodepside
administered as tablets and determine the effect of food on the pharmacokinetics.
Relative Bioavailability Study of Emodepside IR-tablets and Solution
Completed
Bayer
Phase 1
This study evaluates 2 new immediate release (IR)-tablet formulations of emodepside and they
will be compared to the oral liquid service formulation (LSF) used in the FIH Single
Ascending Dose study (DNDi-EMO-001 study) (CT.gov identifier: NCT02661178)
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