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40%
71%
72%
67%
40% of respondents said they were very familiar with biosimilars, 51% said they were only slightly familiar with biosimilars
72% reported that they were likely to prescribe biosimilars if/when they become available in the US, 49% said they were very likely
71% claimed they were likely to prescribe an interchangeable biosimilar, while only 59% would prescribe a non-interchangeable one
67% of gastroenterologists surveyed favor prohibition of indication extrapolation in approval of biosimilars for IBD
In response to biosimilar standards, quality, and safety:
biosimilars.us | What Do Gastroenterologists Think?
What Do Gastroenterologists Think?
80% are very concerned about clinical similarity between the biosimilar and reference product in regards to effectiveness and safety
78% of respondents are very concerned about the immunogenicity and safety of biosimilars
55% of the gastroenterologists surveyed feel pharmacy level substitution should only be permitted with notification of prescriber
35% believe pharmacy level substitution should be ruled out all together
When considering the use of a biosimilar:
80% 78%
55% 35%
69% said their reasoning is lack of experience with biosimilars
65% said more time is needed to examine the effectiveness of biosimilars
Out of those who said they were unlikely to prescribe biosimilars:
69% 65%
Source:Gastro.org,. 'National Survey Reveals Gastroenterologists' Views On Biosimilar Drugs'. N.p., 2015. Web. 17 Aug. 2015.
In late July, the American Gastroenterological Association released findings from a national survey of gastroenterologists on biosimilars and biologics. Biologics are used regularly for the treatment of inflammatory bowel disease (IBD), and biosimilars for the treatment of IBD, such as Remsima/Inflectra are globally on the rise.
This survey reveals that many gastroenterologists are concerned about the safety and efficacy of biosimilars and that some are still unfamiliar with the type of drug itself.