An Observational Study to Evaluate Safety and Efficacy of Remsima™ in Patients With Ankylosing Spondylitis
N/A
Terminated
NCT02557308
| Condition | Ankylosing Spondylitis |
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| Phase | N/A |
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| Sponsor | Celltrion |
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| Status | Terminated |
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| Enrollment | 329 participants |
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| Start date | May 26, 2015 |
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| Completion date | Feb 28, 2021 |
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| Results posted | Dec 9, 2024 |
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Summary
An Observational, Prospective Cohort Study to Evaluate Safety and Efficacy of RemsimaTM in Patients with Ankylosing Spondylitis
The Number and Percentage of Patients With the Following Adverse of Events of Special Interest (ESI)
Duration of study participation (up to 5 years) · Participants
| Remsima | 1 Participants |
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| Switch to Remsima I | 0 Participants |
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| Switch to Remsima II | 0 Participants |
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| Remicade | 0 Participants |
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| Switch to Remicade I | 0 Participants |
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| Switch to Remicade II | 0 Participants |
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Open in BENITIONS
View on ClinicalTrials.gov
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