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NCT01272128: AVAIL

A Multicenter, Prospective Non-interventional Study to Evaluate the Quality of Life in Belgian Patients With CIS or RRMS in Whom Interferon Beta-1a IM Treatment Has Been Initiated

Completed Last updated 16 October 2015
What this trial tests

trial testing Interferon beta-1a in Multiple Sclerosis in 100 participants. Completed in 1 September 2015.

Timeline
1 December 2012
Primary endpoint
1 September 2014
1 September 2015

Quick facts

Lead sponsorBiogen
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date1 December 2012
Primary completion1 September 2014
Estimated completion1 September 2015
Sites17 locations across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Biogen — full company profile →

Who can join

18 and older, any sex, with Multiple Sclerosis. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The primary objective is to assess the quality of life of intramuscular (IM) Interferon Beta-1a in participants with relapsing remitting multiple sclerosis (RRMS) or Clinically Isolated Syndrome (CIS) in a clinical practice setting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Interferon beta-1a

Trials testing the same drug.

Other recruiting trials for Multiple Sclerosis

Currently open trials in the same condition.

Other Biogen trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01272128.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing