An application seeking conditional European approval for avacopan to treat active anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis has been withdrawn.
Vifor Pharma (VTX: VIFN) and ChemoCentryx, a US company that the Swiss drugmaker has a 21.2% stake in, made the announcement on Thursday.
The application had been based only on Phase II data, and now the companies want to apply for full marketing approval in Europe and the USA in 2020, in light of the upcoming availability of data from the pivotal Phase III ADVOCATE trial.
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