The attribution to Lonsurf does not appear to be accurate.
It is an interesting contention as Taiho Oncology's trifluridine/ tipiracil has considerable adverse side effects, modest OS improvements and is short lived compared with SRX's.
The FDA did approve Taiho's Lonsurf on Sep 22, 2015 however that approval on such a date does not allow for such considerable marketing by Taiho and the EMA only approved in the April of 2015 so that contention appears inconsistent with the facts and timelines required for such marketing by Taiho Oncology.
The takeup of such a drug with such adverse side effects produced by a Japanese biopharma is not to my mind compelling.
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