RecruitingPhase 3NCT06847724
Comparative PK, PD, Efficacy, and Safety Assessment of the Proposed Ocrelizumab Biosimilar CYB704 and Ocrevus in Participants With Relapsing Multiple Sclerosis
Studying Opsoclonus-myoclonus syndrome
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
- Sandoz
- Intervention
- CYB704(biological)
- Enrollment
- 175 target
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2025 – 2029
Study locations (30)
- Sandoz Investigational Site, Maitland, Florida, United States
- Sandoz Investigational Site, Ormond Beach, Florida, United States
- Sandoz Investigational Site, Banja Luka, Bosnia and Herzegovina
- Sandoz Investigational Site, Bihać, Bosnia and Herzegovina
- Sandoz Investigational Site 2, Sarajevo, Bosnia and Herzegovina
- Sandoz Investigational Site, Sarajevo, Bosnia and Herzegovina
- Sandoz Investigational Site, Pleven, Bulgaria
- Sandoz Investigational Site 2, Plovdiv, Bulgaria
- Sandoz Investigational Site, Plovdiv, Bulgaria
- Sandoz Investigational Site 2, Sofia, Bulgaria
- Sandoz Investigational Site 3, Sofia, Bulgaria
- Sandoz Investigational Site 4, Sofia, Bulgaria
- Sandoz Investigational Site 5, Sofia, Bulgaria
- Sandoz Investigational Site, Sofia, Bulgaria
- Sandoz Investigational Site, Varaždin, Croatia
- +15 more locations on ClinicalTrials.gov
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.
Open NCT06847724 on ClinicalTrials.govOther trials for Opsoclonus-myoclonus syndrome
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