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Last Updated: April 25, 2024

CLINICAL TRIALS PROFILE FOR EMODEPSIDE


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Clinical Trials for Emodepside

Trial ID Title Status Sponsor Phase Summary
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 >Phase >Summary

Clinical Trial Conditions for Emodepside

Condition Name

Condition Name for
Intervention Trials
Filariasis 2
Hookworm Infections 2
Trichuris Trichiura; Infection 1
Healthy Volunteers 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Ancylostomiasis 2
Filariasis 2
Hookworm Infections 2
Onchocerciasis 1
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Clinical Trial Locations for Emodepside

Trials by Country

Trials by Country for
Location Trials
United Kingdom 3
Tanzania 2
Ghana 1
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Clinical Trial Progress for Emodepside

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 2 3
Phase 1 3
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Completed 3
Recruiting 2
Not yet recruiting 1
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Clinical Trial Sponsors for Emodepside

Sponsor Name

Sponsor Name for
Sponsor Trials
Bayer 4
Drugs for Neglected Diseases 4
Bill and Melinda Gates Foundation 3
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Sponsor Type

Sponsor Type for
Sponsor Trials
Other 11
Industry 4
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