Evaluate the Safe and Effective Use of the Avonex® Single-Use Autoinjector in Multiple Sclerosis Subjects

Completed · Phase 3

Conditions studied: Multiple Sclerosis

In brief

The primary objective of the study was to evaluate the safe and effective use of the single-use autoinjector for the intramuscular (IM) delivery of liquid Avonex® (interferon beta-1a) in participants with multiple sclerosis (MS).

Key facts

Study ID

NCT00828204

Run by

Biogen

People needed

95

Starts

2009-01-01

Expected to finish

2010-10-01

Last updated by the study team

2014-06-03

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local subject privacy regulations.
• Must be 18 to 65 years old, inclusive, at the time of informed consent.
• Must currently be self-administering Avonex Prefilled Syringes to treat MS and must have been self-administering Avonex Prefilled Syringes for the 12 weeks prior to the Screening Visit.
• In the investigator's opinion, subjects must be willing and able to self-administer all injections required by the protocol.
• Must speak English.
• All male subjects and female subjects of child-bearing potential must practice effective contraception during the study.

You may not qualify if…

• History of seizure disorder or unexplained blackouts OR history of a seizure within 3 months prior to the Screening Visit.
• History of suicidal ideation within 3 months prior to Day 1 or an episode of severe depression within 3 months prior to Day 1. Severe depression is defined as any episode of depression that requires hospitalization, or the initiation of antidepressant therapy, or an increase in the dose of an existing regimen of antidepressant therapy. NOTE: Subjects receiving ongoing antidepressant therapy are not excluded from the study unless the dose has been increased within the 3 months prior to the Screening Visit.
• Clinically significant local infection (for example cellulitis, abscess) or systemic infection (pneumonia, septicemia), at the discretion of the Investigator.
• Known history of Human Immunodeficiency Virus (HIV).
• Known history of, or positive test result for hepatitis C virus (test for hepatitis C virus antibody [HCV Ab]) or Hepatitis B virus (test for Hepatitis B Surface Antigen [HBsAg] and/or Hepatitis B Core Antibody [HBcAb]).

Where it is running

• Research Site — Gilbert, Arizona, United States
• Research Site — Phoenix, Arizona, United States
• Research Site — Maitland, Florida, United States
• Research Site — Atlanta, Georgia, United States
• Fort Wayne Neurological Center — Fort Wayne, Indiana, United States
• Research Site — Boston, Massachusetts, United States
• Michigan Institute for Neurological Disorders — Farmington Hills, Michigan, United States
• Research Site — Buffalo, New York, United States
• Comprehensive Multiple Sclerosis Care Center — Patchogue, New York, United States
• Research Site — Charlotte, North Carolina, United States
• Neurology & Neuroscience Associates, Inc. — Akron, Ohio, United States
• Research Site — Dallas, Texas, United States
• Research Site — Round Rock, Texas, United States
• Research Site — Salt Lake City, Utah, United States
• Research Site — Richmond, Virginia, United States
• Research Site — Charleston, West Virginia, United States

Full record on ClinicalTrials.gov

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