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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