| Drug | Class | Adult | Paediatric | Notes |
|---|---|---|---|---|
| ACE inhibitor or ARB[1] | RAS inhibitor | Ramipril 2.5–10 mg PO daily; lisinopril 10–40 mg PO daily; losartan 50–100 mg PO daily; titrate to maximum tolerated | — | All with diabetic CKD or UACR ≥30 mg/g; titrate to maximum tolerated; tolerate eGFR fall up to 30%; check K and creatinine 1–2 weeks after change |
| Dapagliflozin or empagliflozin[1] | SGLT2 inhibitor | Dapagliflozin 10 mg PO daily; empagliflozin 10 mg PO daily | — | Adults with CKD and ACR ≥30 mg/g regardless of diabetes status; start at eGFR ≥20; continue until KRT initiation; sick-day rules; risk of euglycaemic DKA, mycotic genitourinary infection |
| Finerenone[1] | Non-steroidal mineralocorticoid receptor antagonist | 10–20 mg PO once daily — start 10 mg if eGFR 25–60 or K ≤4.8; titrate after 4 weeks | — | Adults with T2DM and CKD with persistent ACR ≥30 mg/g despite optimal RAS inhibitor + SGLT2 inhibitor; avoid eGFR <25 or K >5.0 |
| Atorvastatin or rosuvastatin[1] | HMG-CoA reductase inhibitor | Atorvastatin 20–80 mg PO daily; rosuvastatin 5–20 mg PO daily (renal-adjusted) | — | Primary and secondary cardiovascular prevention in CKD G3a–G5 not on dialysis; benefit unproven in dialysis patients started afresh |
| GLP-1 receptor agonist[1] | Glucagon-like peptide-1 receptor agonist | Semaglutide 0.25 mg SC weekly start, titrate to 1 mg; liraglutide 0.6 mg SC daily start, titrate to 1.8 mg | — | T2DM + CKD with elevated cardiovascular risk; complementary to SGLT2 inhibitor; nausea and weight loss expected; not a primary kidney protector |
Diagnosis, classification by eGFR and albuminuria, prognosis, and progression-modifying therapy in adults with CKD; SGLT2 + RAS + finerenone framework.