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Completed Phase 2 Interventional

A Study to Evaluate Safety and Tolerability of Subcutaneous Doses of MEDI-545 in Subjects With Lupus

ClinicalTrials.gov ID: NCT00657189

Public ClinicalTrials.gov record NCT00657189. 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, 9:10 AM 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 Phase 2A , Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Dose Study to Evaluate the Safety and Tolerability of Multiple Subcutaneous Doses of MEDI-545, A Fully Human Anti-Interferon-Alpha Monoclonal Antibody, In Subjects With Systemic Lupus Erythematosus

Study identification

NCT ID
NCT00657189
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
87 participants

Conditions and interventions

Interventions

  • MEDI-545 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jun 30, 2008
Primary completion
Apr 30, 2010
Completion
Apr 30, 2010
Last update posted
Aug 8, 2016

2008 – 2010

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Research Site Anniston Alabama 36207
Research Site Huntington Beach California 92646
Research Site Upland California 91786
Research Site Colorado Springs Colorado 80910
Research Site Farmington Connecticut 06030-5353
Research Site Clearwater Florida 33765-2616
Research Site Ocala Florida 34474
Research Site Atlanta Georgia 30303
Research Site Decatur Georgia 30033
Research Site Marrietta Georgia 30060
Research Site West Fayetteville Georgia 30269
Research Site Baltimore Maryland 21205
Research Site Lansing Michigan 48910
Research Site Brooklyn New York 10003
Research Site Charlotte North Carolina 28210
Research Site Cincinnati Ohio 45219
Research Site Oklahoma City Oklahoma 73104
Research Site Charleston South Carolina 29406
Research Site Columbia South Carolina 29204
Research Site Houston Texas 77004
Research Site Sugarland Texas 77479
Research Site Seattle Washington 98111

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00657189, 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 Aug 8, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00657189 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →