Choose your kidney diagnosis to see recently approved treatments and actively enrolling clinical trials for that condition — with plain-language evidence and links to ClinicalTrials.gov.
For information only — not medical advice. Always talk to your nephrologist.
17 FDA-approved therapies since 2018 — 8 in the last two years — plus 3 trials enrolling now.
New U.S. FDA approvals for a kidney indication, by year — across IgA nephropathy, lupus nephritis, C3 glomerulopathy, FSGS, diabetic and polycystic kidney disease, and more. Sources on each treatment card below. Verified July 2026.
Blood-pressure control with ACE inhibitors or ARBs, and SGLT2 inhibitors, are standard first-line therapy for most CKD. Your nephrologist typically starts here.
These are newer and recently approved therapies for IgA nephropathy (Berger disease) — not the full standard of care. Ask your care team whether any fit your situation.
Dual endothelin & angiotensin receptor antagonist
Evidence: 42.8% reduction in proteinuria vs 4.4% with irbesartan.
Source: FDA prescribing information; PROTECT, Lancet 2023Verified 2026-07-18
Oral factor B inhibitor (complement pathway)
Evidence: 38.3% reduction in proteinuria vs placebo at 9 months.
Source: FDA prescribing information; APPLAUSE-IgAN, NEJM 2025Verified 2026-07-18
Anti-APRIL monoclonal antibody
Evidence: Significant proteinuria reduction vs placebo; FDA accelerated approval in 2025.
Source: FDA prescribing information (Voyxact); VISIONARY (Phase 3)Verified 2026-07-18
Selective endothelin A receptor antagonist
Evidence: Meaningful proteinuria reduction vs placebo (ALIGN interim); first selective ETA blocker for IgAN.
Source: FDA prescribing information (Vanrafia); ALIGN (Phase 3)Verified 2026-07-18
Targeted-release budesonide (gut-directed)
Evidence: A 9-month course preserved kidney function vs placebo over 2 years.
Source: FDA prescribing information; NefIgArd, Lancet 2023Verified 2026-07-18
Dual BAFF / APRIL inhibitor (TACI-Fc fusion protein)
Approved treatment: Granted FDA accelerated approval on July 7, 2026 to reduce proteinuria in adults with primary IgAN at risk of progression; long-term kidney-function benefit not yet confirmed.
Evidence: 46% reduction in proteinuria from baseline at week 36 (42% vs placebo) in the Phase 3 ORIGIN trial.
Source: FDA prescribing information (Trutakna); ORIGIN 3, NEJM 2026Verified 2026-07-18
Actively enrolling studies related to IgA nephropathy (Berger disease). Whether a trial is right for you — and whether you qualify — is decided by the study team together with your nephrologist.
No actively enrolling trials we're tracking for IgA nephropathy (Berger disease) right now.
For information only — this is not medical advice, and nothing here is a recommendation to start, stop, or switch treatment. Every treatment decision should go through your nephrologist.
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