upper gastrointestinal tract disease gastroesophageal reflux disease
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients treated with vonoprazan for upper gastrointestinal disease 2. Patients receiving written informed consent
Exclusion criteria
Exclusion criteria: 1. Patients discontinuing vonoprazan treatment 2. Patients who are judged by physicians as in appropriate for study enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Concentration of vonoprazan and its metabolite before dosing on day 4 or later | — |
Countries
Japan
Contacts
Hamamatsu University School of Medicine Department of Hospital pharmacy