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Expert Insights: Biosimilar Clinical Development Boom for Three Roche Oncology Products

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09:18, January 10 2018

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Heather Leach, GlobalData, explores how the growth of biosimilars has impacted the oncology space

Over the course of 2017, there has been an explosion of news regarding biosimilars for oncology products. This year marked the first U.S. and European approvals for biosimilars in oncology, with the February 2017 approval of Celltrion’s rituximab biosimilar by the EMA (which is marketed under four names, Blitzima, Ritemvia, Rituzena, and Truxima, and officially launched in April) and the September 2017 FDA approval of Amgen’s Mvasi, a bevacizumab biosimilar. Counting the U.S. and EU, there are now biosimilar products approved for three key drugs in Roche’s oncology portfolio: Avastin (bevacizumab), Herceptin (trastuzumab), and Rituxan (rituximab). In the U.S., there is another approved trastuzumab biosimilar in addition to the above-mentioned bevacizumab product, although Avastin and Herceptin will not lose U.S. patent protection until 2019. The EU has seen a similar surge, with an additional competing rituximab biosimilar from Sandoz and one trastuzumab biosimilar.

GlobalData predicts that biosimilar news will continue to escalate in the coming years. An analysis of clinical trials for all planned, ongoing, and completed trials revealed a total of 135 trials of biosimilars for four oncology products. Roche’s three products are under threat with a total of 36, 47, and 47 trials for rituximab, bevacizumab, and trastuzumab biosimilars, respectively, by various other developers. There is far less commercial interest in developing a biosimilar for Eli Lilly’s Erbitux (cetuximab), a product with 2016 sales of $1.6B. Compared with $7.6B, $7.1B, and $7.1B in 2016 sales for Rituxan, Avastin, and Herceptin, respectively, it is obvious why biosimilar developers are keen to cash in with a copy of these blockbuster drugs.

Among the analyzed trials, there were 57 ongoing and completed Phase III clinical trials. By drug, this represents two trials for cetuximab, 18 each for rituximab and trastuzumab, and 19 for bevacizumab. Close to half of these trials, 43.9 percent (25 out of 57), were completed trials. Of particular interest, rituximab and trastuzumab seem to have a higher proportion of completed trials than bevacizumab. This large number of completed Phase III trials could signal an increased number of filings for oncology biosimilars in the near future.

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