Crohn'
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients receiving IFX more than 3 times previously
Exclusion criteria
Exclusion criteria: Patients receiving IFX with 10 mg/kg dose Patients receiving IFX at interval of less than 6 weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical remission rate after 104 weeks (Interim analysis performed in 52 weeks) | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation with change of IFX dose and CRP value or fecal concentration of calprotectin | — |
Countries
Japan
Contacts
NationalOrganizationHospital Fukuyama medical center Department of Gastroenterology