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The principal endpoint compared the ACR20 measurements at week 24. The ACR20 was within the prespecified margin for ABP 501 compared to adalimumab, showing clinical equivalence. Safety and immunogenicity of ABP 501 were comparable to adalimumab. Crucial secondary endpoints included ACR50, DAS and ACR70 28-CRP. The positive results from Amgen's biosimilar Phase 3 rheumatoid arthritis research showed clinical equivalence in efficacy, and comparable basic safety and immunogenicity, to adalimumab. Amgen's success on both our ABP 501 psoriasis and arthritis rheumatoid studies underscores our knowledge in the research and advancement of high-quality biologic therapies, said Sean E.