Although Novartis’s immunoglobulin A nephropathy (IgAN) franchise will face considerable competition from other firms, the accelerated approval in the US of Vanrafia (atrasentan) further solidifies its market position by helping it to cover multiple stages of the pathogenesis of IgAN.
Key Takeaways
- The FDA gave accelerated approval to Novartis’s Vanrafia for IgA nephropathy, making it the second drug in the company’s portfolio for the disease, after Fabhalta.
The US Food and Drug Administration approved Vanrafia for proteinuria reduction in primary IgAN on 2 April, making it the...
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