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NCT00828204 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by Biogen.

Completed
Registry status
Phase 3
Development phase
95
Enrollment target

NCT00828204: Completed Phase 3 study, sponsored by Biogen.

NCT00828204 is a Phase 3 study that has completed, run by Biogen. The registered enrollment target is 95 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00828204, a Phase 3 study, has completed, sponsored by Biogen.

COMPLETED
Registry status
Phase 3
Development phase
95 participants
Enrollment target

Study Summary

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).

Primary Outcome

A trainer/observer documented the participant's ability to self-inject with the Avonex single-use autoinjector and completed an observation form. Overall success in using the device for each participant was defined as no failures occurring in any step (ie, device set-up, self-administration of injection, and capping/disposal of the device) during the participant's use of the single-use Avonex autoinjector.

Interventions

  • DEVICE single-use autoinjector with a prefilled liquid Avonex syringe
  • DEVICE Avonex prefilled syringe via manual IM injection
  • DRUG BG9418 (interferon beta-1a)

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2009-01
Est. Completion 2010-10
Phase Phase 3
Biogen

334 total trials

What the finished NCT00828204 record still lists

NCT00828204 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 95 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 3 interventions - of which single-use autoinjector with a prefilled liquid Avonex syringe is the first listed.

NCT00828204 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00828204 about?

NCT00828204 is a clinical study titled "Evaluate the Safe and Effective Use of the Avonex® Single-Use Autoinjector in Multiple Sclerosis Subjects". 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).

What is the current status of trial NCT00828204?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 95 participants. The study started on 2009-01. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00828204?

The interventions under investigation include: single-use autoinjector with a prefilled liquid Avonex syringe (DEVICE), Avonex prefilled syringe via manual IM injection (DEVICE), BG9418 (interferon beta-1a) (DRUG).

Who is sponsoring clinical trial NCT00828204?

This trial is sponsored by Biogen, which has 334 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00828204's enrollment target sits among peer trials

95 1719th of 2000 higher than 282 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00828204, the US trial registry maintained by the National Library of Medicine. NCT00828204 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.