Active, not recruitingPhase 2NCT06293365
Two-period Crossover Study to Demonstrate the Comparability of Pharmacokinetics of Subcutaneous Ianalumab Between 2mL Auto-injector/2mL PFS with1mL Pre-filled Syringe in Adult Participants With Autoimmune Disease
Studying Systemic lupus erythematosus
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
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- VAY736 1ml PFS(biological)
- Enrollment
- 155 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2024 – 2029
Study locations (30)
- Pinnacle Research Group Llc, Anniston, Alabama, United States
- Providence Medical Foundation, Fullerton, California, United States
- Advanced Medical Research, La Palma, California, United States
- Conquest Research, Winter Park, Florida, United States
- Parris and Associates Rheumatology, Lawrenceville, Georgia, United States
- Indiana Univ School of Dentistry, Indianapolis, Indiana, United States
- Ochsner Health System, Baton Rouge, Louisiana, United States
- Ahmed Arif Medical Research Center, Grand Blanc, Michigan, United States
- Paramount Med Rsrch and Consult LLC, Middleburg Heights, Ohio, United States
- RAO Research LLC, Oklahoma City, Oklahoma, United States
- Altoona Center for Clin Res, Duncansville, Pennsylvania, United States
- West Tennessee Research Institute, Jackson, Tennessee, United States
- Shelby Research LLC, Memphis, Tennessee, United States
- Novel Research LLC, Bellaire, Texas, United States
- Southwest Rheum Rsrch LLC, Mesquite, Texas, United States
- +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.
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