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Completed Phase 1 Interventional

A Study to Evaluate the Safety and Tolerability of Multiple Intravenous Doses of MEDI 545 in Patients With Systemic Lupus Erythematosus

ClinicalTrials.gov ID: NCT00482989

Public ClinicalTrials.gov record NCT00482989. 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 May 5, 2026, 3:18 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 Phase 1b, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety and Tolerability of Multiple Intravenous Doses of MEDI-545, a Fully Human Anti-Interferon-Alpha Monoclonal Antibody, in Patients With Systemic Lupus Erythematosus

Study identification

NCT ID
NCT00482989
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
MedImmune LLC
Industry
Enrollment
183 participants

Conditions and interventions

Conditions

Interventions

  • MEDI 545 Biological
  • Placebo Other

Biological · Other

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
May 31, 2007
Primary completion
Jun 30, 2010
Completion
Aug 31, 2010
Last update posted
Jul 10, 2012

2007 – 2010

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Research Site Anniston Alabama 36207
Research Site La Jolla California 92037-0943
Research Site Los Angeles California 90048
Research Site Clearwater Florida 37765
Research Site Fort Lauderdale Florida 33334
Research Site Ocala Florida 34474
Research Site Tampa Florida 33614
Research Site Shreveport Louisiana 71130
Research Site Baltimore Maryland 21205
Research Site Bethesda Maryland 20892
Research Site Manhasset New York 11030
Research Site New York New York 10003
Research Site New York New York 10021
Research Site Greenville North Carolina 27858
Research Site Oklahoma City Oklahoma
Research Site Portland Oregon 97223
Research Site Dallas Texas 75235
Research Site Dallas Texas 75390-8577

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00482989, 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 Jul 10, 2012 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00482989 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →