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Celltrion’s Remsima SC Biosimilar Starts Strong In EU5 Countries

New Study Follows Approval For IBD Indications Last Year

 
• By Dean Rudge

Celltrion is capitalizing on the earlier strength of its intravenous Remsima formulation to make waves with its innovative subcutaneous version, according to the results of a new study sampling nearly 250 gastroenterologists in EU5 countries.

IBD
The report sampled 246 EU5 gastroenterologists in November and December last year. • Source: Shutterstock

Less than a year after its introduction in Europe, Celltrion’s Remsima SC subcutaneous infliximab biosimilar has captured material market share among inflammatory bowel disease patients in the EU5 countries, including the UK, according to a newly-released report sampling nearly 250 EU5 gastroenterologists in November and December last year.

Aided by the cannibalization of the intravenous formulation of Remsima – a biosimilar to Janssen’s Remicade – and the decline in use of AbbVie’s Humira (adalimumab) for inflammatory bowel disease, Remsima SC was able to achieve an 8% patient share among ulcerative colitis infliximab

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