RecruitingPhase 2NCT07203001
A Phase II Trial to Evaluate the Clinical Efficacy, Safety and Tolerability of MAS825 in Pediatric and Adult Participants With Still's Disease
Studying Adult-onset Still disease
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
- Novartis Pharmaceuticals
- Intervention
- MAS825(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 1-100 years · All sexes
- Timeline
- 2025 – 2029
Study locations (20)
- Cincinnati Childrens Hospital, Cincinnati, Ohio, United States
- Legacy Emanuel Research Hosp Portland, Portland, Oregon, United States
- Novartis Investigative Site, Montreal, Quebec, Canada
- Novartis Investigative Site, Bordeaux, France
- Novartis Investigative Site, Bron, France
- Novartis Investigative Site, Le Kremlin-Bicêtre, France
- Novartis Investigative Site, Lille, France
- Novartis Investigative Site, Paris, France
- Novartis Investigative Site, Sankt Augustin, North Rhine-Westphalia, Germany
- Novartis Investigative Site, Heidelberg, Germany
- Novartis Investigative Site, Münster, Germany
- Novartis Investigative Site, Florence, FI, Italy
- Novartis Investigative Site, Genova, GE, Italy
- Novartis Investigative Site, Roma, RM, Italy
- Novartis Investigative Site, Utrecht, Netherlands
- +5 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.
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