drugset / Trial / NCT06456567

A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-2)

NCT06456567

Phase 3 Withdrawn Vor Biopharma
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of moderately to severely active SLE.

Timeline

Start
2024-09
Primary completion
2025-01-02
Completion
2025-01-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Telitacicept Protein / enzyme biologic Subcutaneous