drugset / Trial / NCT05123586

A IMMA Master Protocol: A Study of LY3361237 in Participants With at Least Moderately Active Systemic Lupus Erythematosus

NCT05123586 ↗

Phase 2 Terminated 85 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to assess the efficacy and safety of LY3361237 in participants with at least moderately active systemic lupus erythematosus (SLE). Study will last up to 34 weeks and may include up to 15 visits.

Timeline

Start
2022-03-07
Primary completion
2023-12-29
Completion
2023-12-29

Outcome

Outcome not reported

Stopped: “Study terminated due to lack of efficacy”

Drugs

EvaluationDrugModalityDoseRoute
Subject VENANPRUBART Monoclonal antibody — Subcutaneous