RecruitingPhase 2NCT06581198
A Study of Rapcabtagene Autoleucel in Active, Refractory Systemic Lupus Erythematosus (SLE) or Lupus Nephritis (LN) Patients (AUTOGRAPH - SLE/LN)
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
- rapcabtagene autoleucel(biological)
- Enrollment
- 179 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2024 – 2032
Study locations (30)
- University Of Alabama, Birmingham, Alabama, United States
- Loma Linda University, San Bernardino, California, United States
- UCSF, San Francisco, California, United States
- Sutter Health Network, San Pablo, California, United States
- Ann and Robert H Lurie Childs Hosp, Chicago, Illinois, United States
- Northwestern University, Chicago, Illinois, United States
- University Of Iowa, Iowa City, Iowa, United States
- University of Kentucky, Lexington, Kentucky, United States
- Tufts Medical Center, Boston, Massachusetts, United States
- Boston Medical Center, Boston, Massachusetts, United States
- WA Uni School Of Med, St Louis, Missouri, United States
- Oregon Health Sciences University, Portland, Oregon, United States
- Univ Of TX MD Anderson CC, Houston, Texas, United States
- University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- LDS Hospital, Salt Lake City, Utah, 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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