Table 1.
Emerging therapeutic approaches for cardiovascular complications in CKD.
| Medication | Clinical Trial | Population (Number of Patients) |
Intervention | Comparison | Outcome | Notable Effects/ Considerations |
Ref |
|---|---|---|---|---|---|---|---|
| Atrasentan | SONAR | Diabetic nephropathy, CKD patients (2648) | Endothelin receptor antagonist (atrasentan) | Placebo or standard therapy | Slows CKD progression and reduces vasoconstriction, fibrosis, inflammation, and cardiovascular risk | Particularly beneficial in diabetic nephropathy | [179] |
| Finerenone | FIDELIO-DKD | Diabetic kidney disease patients with CKD (5734) | Non-steroidal mineralocorticoid receptor antagonist | Placebo or steroidal MRAs | Reduced CKD progression and cardiovascular events | Lower risk of hyperkalemia compared to steroidal MRAs | [180] |
| Finerenone | FIGARO-DKD | Diabetic kidney disease patients with earlier-stage CKD (7352) | Non-steroidal mineralocorticoid receptor antagonist | Placebo or steroidal MRAs | Reduced cardiovascular events and slower CKD progression | Beneficial even in patients with early CKD | [181] |
| Empagliflozin | EMPA-KIDNEY | CKD patients, particularly with type 2 diabetes (6609) | SGLT2 inhibitor | Placebo or standard therapy | Decreases CKD progression and cardiovascular mortality | Provides cardiovascular and renal protection independent of glycemic control | [183] |
| Semaglutide | FLOW | CKD patients with type 2 diabetes (3000) | GLP-1 receptor agonist | Placebo or standard therapy | Slowed CKD progression | Potential to slow kidney disease progression alongside glucose control | [184] |
| Semaglutide | SELECT | Obese patients with cardiovascular disease (17,604) | GLP-1 receptor agonist | Placebo or standard therapy | Reduced risk of MACE by 20% in patients with obesity and cardiovascular disease | Cardiovascular benefits independent of glucose control | [185] |
| CRISPR Gene Therapy | Ongoing research | Patients with genetic causes of CKD (ongoing) | CRISPR-based gene editing | Standard treatment or no gene therapy | Potential for long-lasting correction of genetic mutations; still experimental | Promising but undergoing ongoing research | [177] |
| Canakinumab | CANTOS | CKD patients with increased cardiovascular risk (10,061) | IL-1β inhibitor | Placebo or standard therapy | Reduces cardiovascular events by targeting inflammatory pathways | Anti-inflammatory effects | [191] |
| Ziltivekimab | RESCUE | CKD patients with high CRP levels (623) | IL-6 inhibitor | Placebo | Reduces inflammation and thrombosis | Shows promise in managing inflammation-related CKD complications | [192] |
| Mesenchymal Stem Cells (MSCs) | Early-stage trials | CKD patients, particularly with diabetic or hypertensive nephropathy (ongoing) | Stem cell therapy | Standard therapy or no MSC therapy | Repairs damaged kidney tissue and reduces fibrosis and inflammation; early-stage trials | Promising for nephroprotection and delivery of Klotho | [208,209] |