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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 Oct 23, 2026, 8:21 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 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the safety and tolerability of multiple IV doses of the MEDIMUNNE antibody in adult patients with SLE.

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

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
Jun 2007 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
Sep 2010 (Actual)
Last update posted
Jul 11, 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 11, 2012 · Synced Oct 23, 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 public registry record, listed eligibility criteria, and available contact information for NCT00482989 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →