FDA approves a new treatment for primary immunoglobulin A nephropathy

FDA

25 November 2025 - The US FDA has granted accelerated approval to Voyxact (sibeprenlimab-szsi) injection to reduce proteinuria in adults with primary immunoglobulin A nephropathy at risk for disease progression. 

The efficacy and safety of Voyxact were evaluated in a randomised, double-blind, placebo-controlled trial in adults with biopsy-confirmed immunoglobulin A nephropathy.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Registration