Relapsing-remitting Multiple Sclerosis Clinical Trial
Official title:
The AVANTAGE Study - A Randomized, Multicenter, Phase IV, Open-label Prospective Study Comparing Injection Site Reaction and Injection Site Pain in Patients With Relapsing Remitting Multiple Sclerosis (RRMS) or After a First Demyelinating Event Suggestive of MS Newly Started on Interferon Beta-1b (Betaferon®) or Interferon Beta-1a (Rebif®).
The purpose of this study is to compare the injection site reaction and injection site pain after subcutaneous administration of either Betaferon 250µg or Rebif 44µg using different autoinjectors.
Original French title of the study: Etude de phase IV, multicentrique, randomisée, ouverte,
comparant les réactions et la douleur aux sites d'injection après administration
sous-cutanée d'interféron β-1b (Betaferon®) ou interféron β-1a (Rebif®) pendant la période
de trois mois d'initiation de la thérapie chez des patients atteints d'une forme
récurrente/rémittente de sclérose en plaques.
The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been
renamed to Bayer HealthCare AG, Germany. Bayer HealthCare AG, Germany is the sponsor of the
trial.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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