drugset / Trial / NCT05917288

A Study of Belimumab in Chinese Pediatric Participants With Systemic Lupus Erythematosus

NCT05917288

Phase 1 Completed 16 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the pharmacokinetic characteristics and safety of belimumab subcutaneous (SC) in Chinese pediatric participants with SLE who have completed 48 weeks belimumab Intravenous (IV) treatment in 213560 study (NCT04908865)

Timeline

Start
2023-07-07
Primary completion
2024-10-30
Completion
2024-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Belimumab Monoclonal antibody 200 mg Subcutaneous