CLINICAL TRIALS PROFILE FOR EMODEPSIDE
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Clinical Trials for Emodepside
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT02661178 ↗ | 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. |
NCT02661178 ↗ | 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. |
NCT02661178 ↗ | 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. |
NCT03383523 ↗ | 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) |
NCT03383523 ↗ | Relative Bioavailability Study of Emodepside IR-tablets and Solution | Completed | Bill and Melinda Gates Foundation | 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) |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for Emodepside
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Clinical Trial Locations for Emodepside
Clinical Trial Progress for Emodepside
Clinical Trial Phase
Clinical Trial Sponsors for Emodepside
Sponsor Name