Active, not recruitingPHASE1, PHASE2NCT06015230
Clinical Study to Investigate the Safety, Tolerability, and Pharmacokinetics of GR1603 in SLE
Studying Autosomal 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
- Genrix (Shanghai) Biopharmaceutical Co., Ltd.
- Principal Investigator
- xiaofeng zeng, PHDPeking Union Medical College Hospital
- Intervention
- low dose GR1603 in phase Ⅰb(biological)
- Enrollment
- 136 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2022 – 2028
Study locations (1)
- Peking union Medical Hosipital, Beijing, Beijing Municipality, China
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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