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Evaluation of the Switch From the Original Infliximab ( REMICADE®) to Its Biosimilar (INFLECTRA®) in Daily Practice at Cochin Hospital (SIC)
The purpose of this study is to evaluate the effectiveness of the switch from the original infliximab ( REMICADE®) to its biosimilar (INFLECTRA®) in all the patients at Cochin hospital receiving REMICADE® for either a rheumatic, gastro-enterologic or ophthalmic condition
Details
| Lead sponsor | Assistance Publique - Hôpitaux de Paris |
|---|---|
| Status | COMPLETED |
| Enrolment | 262 |
| Start date | 2015-10 |
| Completion | 2016-06-29 |
Conditions
- Rheumatoid Arthritis
- Spondyloarthritis
- Crohn's Disease
- Uveitis
Interventions
- Switch from REMICADE® to INFLECTRA®
Primary outcomes
- Percentage of patients continuing INFLECTRA® — after the third infusion of INFLECTRA®, up to 24 weeks
Evaluation of the percentage of patients continuing INFLECTRA® after its third infusion
Countries
France