Active, not recruitingNCT05866614
A Study to Evaluate the Safety of Remsima® SC in the Treatment of RA, AS, PsA and Ps
Studying NON RARE IN EUROPE: Rheumatoid arthritis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celltrion
- Intervention
- Remsima IV(drug)
- Enrollment
- 881 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2027
Study locations (1)
- CHU Purpan Hôpital Pierre Paul Riquet, Toulouse, France, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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