ContRAst-1 und ContRAst-2 erreichten ihre primären Endpunkte, d. h. ein statistisch signifikantes Ansprechen auf die ACR20-Bewertungskriterien (American College of Rheumatology-Kriterien), im Vergleich zu Placebo in Woche 12 bei Patienten mit unzureichendem Ansprechen auf Methotrexat (ContRAst-1) und konventionelle synthetische oder
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