Phase III Results Position Selecta/Sobi’s SEL-212 As Tough Competition For Krystexxa In Gout

Analysts pointed to SEL-212’s more favorable dosing and adverse event profile with fewer limitations that may harm compliance versus Krystexxa from Horizon, which is soon to be acquired by Amgen.

Selecta and Sobi posted positive topline results from their Phase III trials of SEL-212 in chronic refractory gout • Source: Shutterstock

Selecta Biosciences, Inc.’s and Swedish Orphan Biovitrum AB’s (Sobi’s) Phase III results for SEL-212 in gout will likely be sufficient for the drug’s US Food and Drug Administration approval, but they also point to potential commercial advantages over Horizon Therapeutics plc’s Krystexxa (pegloticase) in terms of adverse events, convenience and issues that affect adherence.

Selecta and Sobi announced 21 March positive topline results from the DISSOLVE I and DISSOLVE II trials, which were placebo-controlled...

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