drugset / Trial / NCT05123586
A IMMA Master Protocol: A Study of LY3361237 in Participants With at Least Moderately Active Systemic Lupus Erythematosus
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | VENANPRUBART | Monoclonal antibody | — | Subcutaneous |