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Published in 2018 at "Revista Espanola De Enfermedades Digestivas"
DOI: 10.17235/reed.2018.5456/2018
Abstract: : In 2013, the European Medicines Agency (EMA) approved the biosimilar infliximab (CT-P13) for the full range of indications of the originator product, based on data from two trials conducted in rheumatoid arthritis and ankylosing…
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Keywords:
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