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Clinical trialNCT00099489CompletedPhase 2Interventional

Safety and Efficacy of Avonex in Subjects With Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)

SponsorBiogenEnrollment67Chronic Inflammatory Demyelinating Polyradiculoneuropathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to determine whether AVONEX (Interferon Beta-1a), when compared to placebo, reduces the total dose of IVIg that is administered after Visit 5 and through Visit 9 (Week 32, End of Study).

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

20 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Liverpool Hospital

    Liverpool, New South Wales, Australia

  • Institute of Clinical Neurosciences

    Sydney, New South Wales, Australia

  • St. Vincent'S Hospital

    Fitzroy, Victoria, Australia

  • Royal Melbourne Hospital

    Parkville, Victoria, Australia

Canada
  • London Health Sciences Center

    London, Ontario, Canada

  • Montreal Neurological Hospital

    Montreal, Quebec, Canada

United Kingdom
  • Guy'S Hospital/dept. of Neuroimmunology

    London, United Kingdom

United States
  • Phoenix Neurological Associates, Ltd.

    Phoenix, Arizona, United States

  • Neuromuscular Research Center

    Scottsdale, Arizona, United States

  • University of Florida, Jacksonville

    Jacksonville, Florida, United States

  • University of Miami

    Miami, Florida, United States

  • University of Kansas

    Kansas City, Kansas, United States

  • Louisiana State University

    New Orleans, Louisiana, United States

  • Harvard University/mgh

    Boston, Massachusetts, United States

  • Tufts University/ St. Elizabeths

    Boston, Massachusetts, United States

  • University of Minnesota

    Minneapolis, Minnesota, United States

  • Weill Medical College of Cornell University

    New York, New York, United States

  • Raleigh Neurology Associates

    Raleigh, North Carolina, United States

  • University of Texas Southwestern

    Dallas, Texas, United States

  • University of Utah

    Salt Lake City, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
29 Feb 2004
Primary completion
28 Feb 2006
Completion
28 Feb 2006
Last update posted
5 Mar 2010
Registered enrollment
67
Registry id
NCT00099489

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.