VERA · Vera Therapeutics, Inc. · Documents
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Vera Therapeutics reported $10.3 million in Trutacna revenue and approximately 700 patient start forms. It submitted an SBLA seeking full FDA approval, anticipated in mid-2027, supported by a 76% reduction in kidney disease progression risk through 104 weeks.
Vera Therapeutics’ TRUTAKNA received FDA accelerated approval on July 7, 2026, for adults with primary IgAN at risk for progression; it generated $10.3 million in product revenue through September 30, 2026, while requesting full approval on November 3, 2026.
Vera Therapeutics reported a 76% reduction in composite kidney progression through week 104 and an annualized eGFR difference of 5 mL per minute per year for atachycept. An FDA submission supporting potential full approval is planned for 2027.