ProKidney Corp. reported cash, cash equivalents, and marketable securities totaling $271.7 million as of September 30, 2025, compared to $358.3 million at the end of 2024. The company expects these funds to support operations into mid-2027. More than half of the patients required for the Phase 3 PROACT 1 study for rilparencel have been enrolled, with topline results expected in the second quarter of 2027. The FDA confirmed that estimated glomerular filtration rate (eGFR) slope can serve as the primary endpoint for a Biologics License Application submission for rilparencel under the accelerated approval pathway. Full Phase 2 results for rilparencel were recently presented, showing statistically significant stabilization of kidney function.