drugset / Trial / NCT05278663

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of E6742 in Systemic Lupus Erythematosus Participants

NCT05278663 ↗

Phase 1/2 Completed 26 enrolled Eisai Inc.
RandomizedSequentialDouble-blindTreatment

Summary

The primary purpose of the study is to evaluate the safety and tolerability of multiple oral doses of E6742 in participants with systemic lupus erythematosus (SLE).

Timeline

Start
2022-04-14
Primary completion
2023-09-04
Completion
2023-09-04

Drugs

EvaluationDrugModalityDoseRoute
Subject E6742 Unknown 100 mg Oral
Subject E6742 Unknown 200 mg Oral