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Terminated Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT05123586

Public ClinicalTrials.gov record NCT05123586. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Two-Arm, Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of LY3361237 as a Treatment for Adults With At Least Moderately Active Systemic Lupus Erythematosus

Study identification

NCT ID
NCT05123586
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
85 participants

Conditions and interventions

Interventions

  • LY3361237 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 6, 2022
Primary completion
Dec 28, 2023
Completion
Dec 28, 2023
Last update posted
Jan 19, 2025

2022 – 2023

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Arizona Arthritis & Rheumatology Associates, P. C. Mesa Arizona 85210
Arizona Arthritis & Rheumatology Associates Phoenix Arizona 85037
Arizona Arthritis & Rheumatology Research - Sun City Sun City Arizona 85351
Newport Huntington Med Grp Huntington Beach California 92648
Desert Medical Advances Rancho Mirage California 92270
Clinical Research of West Florida, Inc. (Clearwater) Clearwater Florida 33765
Ezy Medical Research Miami Florida 33175
Clinical Research of West Florida Tampa Florida 33606
Atlanta Research Center for Rheumatology Marietta Georgia 30060
Qualmedica Research, LLC Evansville Indiana 47715
Tekton Research, Inc Wichita Kansas 67218
Clinvest Research LLC Springfield Missouri 65807
SUNY Upstate Medical University Syracuse New York 13210
University of North Carolina Hillsborough North Carolina 27278
Paramount Medical Research Middleburg Heights Ohio 44130
Tekton Research, Inc. Moore Oklahoma 73160
Tekton Research, Inc Austin Texas 78745
Rheumatology Center Of Houston Houston Texas 77004
Houston Rheumatology & Arthritis Specialists Katy Texas 77494

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05123586, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 19, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05123586 live on ClinicalTrials.gov.

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