None
Conditions
Interventions
Phase1: Baseline data is obtained by orally administering Atobacon proguanil combination tablet. Phase2: Inhibitor 1 Esomeprazole magnesium hydrate 20 mg is continuously administered orally for 5 con
Sponsors
Kameda Medical Center
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Healthy volunteers
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Concentration of esomeprazole, Vonoprazan in plasma Plasma and urinary concentrations of atovaquone / cycloguanil | — |
Secondary
| Measure | Time frame |
|---|---|
| endogenous metabolites which change with administration of inhibitor are identified. | — |
Countries
Japan
Contacts
Public Contactryokan funakoshi
Kameda Medical Center Pharmacy
Outcome results
None listed