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Etude de phase IV, milticentrique, randomisee, ouverte, comparant les reactions et la douleur aux sites d'injection apres administrartion sous-cutaneed' interferon beta-1b (Betaferon(RM)) ou interferon beta-1a (Rebif(RM)) pendant la periode de troi mois d'initiation de la therapie chez des patients atteints d'une forme recurrente/remittente de sclerose en plaques. AVANTAGE: Analyse comparative des reactions aux sites d'injection sur venues apres administration de betaferon 25 microg ou rebif 44 microg

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Etude de phase IV, milticentrique, randomisee, ouverte, comparant les reactions et la douleur aux sites d'injection apres administrartion sous-cutaneed' interferon beta-1b (Betaferon(RM)) ou interferon beta-1a (Rebif(RM)) pendant la periode de troi mois d'initiation de la therapie chez des patients atteints d'une forme recurrente/remittente de sclerose en plaques. AVANTAGE: Analyse comparative des reactions aux sites d'injection sur venues apres administration de betaferon 25 microg ou rebif 44 microg

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 03 Nov 2021

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At a glance

  • Drugs Interferon beta-1b (Primary) ; Interferon beta-1a
  • Indications Multiple sclerosis
  • Focus Adverse reactions
  • Acronyms AVANTAGE
  • Sponsors Bayer HealthCare Pharmaceuticals

    • Most Recent Events

    • 12 Jan 2012 Company (Bayer Healthcare) added as reported by ClinicalTrials.gov.
    • 25 Sep 2008 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 25 Sep 2008 Actual end date changed from 1 Dec 2007 to 1 May 2008 as reported by ClinicalTrials.gov.

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