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Completed Phase 2 Interventional Results available

A Study to Evaluate the Long-Term Safety of MEDI-545 in Adult Participants With Systemic Lupus Erythematosus or Myositis

ClinicalTrials.gov ID: NCT00979654

Public ClinicalTrials.gov record NCT00979654. 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 Sep 6, 2026, 1:16 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 2 Open-label Study to Evaluate the Long-term Safety of Sifalimumab in Adult Subjects With Systemic Lupus Erythematosus or Myositis

Brief summary

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

The objective of this study is to assess the safety and tolerability of sifalimumab in adult participants with active systemic lupus erythematosus (SLE) or active dermatomyositis (DM) or polymyositis (PM) who participated in the following clinical studies: MI-CP151, MI-CP152, or MI-CP179.

Study identification

NCT ID
NCT00979654
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
118 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 99 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
Jul 31, 2010
Primary completion
Feb 28, 2015
Completion
Feb 28, 2015
Last update posted
Oct 26, 2016

2010 – 2015

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Research Site Anniston Alabama
Research Site Scottsdale Arizona
Research Site San Leandro California
Research Site Upland California
Research Site Colorado Springs Colorado
Research Site Fort Lauderdale Florida
Research Site Ocala Florida
Research Site Tampa Florida
Research Site Baltimore Maryland
Research Site Cumberland Maryland
Research Site Boston Massachusetts
Research Site Ann Arbor Michigan
Research Site Lansing Michigan
Research Site Lake Success New York
Research Site Manhasset New York
Research Site New York New York
Research Site Charlotte North Carolina
Research Site Cincinnati Ohio
Research Site Oklahoma City Oklahoma
Research Site Portland Oregon
Research Site Duncansville Pennsylvania
Research Site Columbia South Carolina
Research Site Dallas Texas
Research Site Houston Texas

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00979654, 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 Oct 26, 2016 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00979654 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →