drugset / Trial / NCT07515014
A Study of E6742 in Participants With Systemic Lupus Erythematosus
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | E6742 | Unknown | — | Oral |