drugset / Trial / NCT07515014

A Study of E6742 in Participants With Systemic Lupus Erythematosus

NCT07515014 ↗

Phase 2 Recruiting 256 enrolled Eisai Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of the study is to demonstrate the efficacy based on dose response of E6742 compared with placebo as defined by the proportion of participants achieving a response using the British Isles Lupus Assessment Group (BILAG) based Composite Lupus Assessment (BICLA) with a low dose of oral corticosteroids (OCS) (prednisone or equivalent) at Week 24 in participants with systemic lupus erythematosus (SLE).

Timeline

Start
2026-03-31
Primary completion
2028-08-05
Completion
2029-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject E6742 Unknown — Oral