An interim analysis of the small, single-arm ANNEXA-4 study of Portola Pharmaceuticals Inc.'sAndexXa antidote for Factor Xa anticoagulants raised questions about an 18% rate of thrombotic events, but the company explains that this is in line with what would be expected for an at-risk, elderly patient population.
Portola Defends AndexXa Antidote Safety, Says Thrombotic Events In Line
Interim analysis of ANNEXA-4 study published in NEJM supports case for AndexXa approval, but 18% thrombosis rate raised some eyebrows.

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Sponsors of three drugs that are in the final stages of the EU regulatory review cycle are due to make the case for marketing approval before the European Medicines Agency.
The European Medicines Agency is this week set to issue an opinion on whether pan-EU marketing should be granted to Lilly’s Alzheimer’s disease drug donanemab.
The European Medicines Agency is re-evaluating the marketing application for Aplidin. The initial application was rejected in 2018, but that rejection was revoked last year following a court case for another company’s drug that clarified impartiality requirements for experts consulted by the EMA.