Table 2.
Clinical trials | Clinical trials’ number | Year | Phase | Paticipants (n) | Intervention | Follow-up | Main outcome |
---|---|---|---|---|---|---|---|
Dipeptidyl peptidase-4 (DPP-4) inhibitors | |||||||
CARMELINA502 | NCT01897532 | 2013–2018 | 4 | 6991 |
I: Linagliptin C: Placebo |
2.2 years | Reduced proteinuria, control blood glucose. |
Glucagon-like peptide-1 receptor (GLP-1) agonizts | |||||||
REWIND503 | NCT01394952 | 2011–2018 | 3 | 9901 |
I: Dulaglutide C: placebo |
5.4 years | Reduced compound renal outcome. |
PIONEER 5504 | NCT02827708 | 2016–2018 | 3 | 424 |
I: Semaglutide C: Placebo |
0.54 years | Effective in patients with type 2 diabetes and moderate renal impairment, but with higher adverse events. |
BETENT-4505 | NCT03730662 | 2018–2021 | 3 | 2002 |
I: Tirzepatide C: Insulin Glargine |
2 years | Slowed down eGFR decline rate, reduced UACR (urinary albumin creatinine ratio). |
Sodium-glucose cotransporter-2 (SGLT2) inhibitors | |||||||
DAPA-CKD506 | NCT03036150 | 2017–2020 | 3 | 4304 |
I: Dapagliflozin C: Placebo |
3.2 years | Reduced the risk of GFR and major renal and cardiovascular adverse events in diabetic and non-diabetic patients with chronic kidney disease. |
CREDENCE487 | NCT02065791 | 2014–2018 | 3 | 4401 |
I: Canagliflozin C: Placebo |
2.62 years | Reduced the risk of kidney failure and cardiovascular events. |
SCORED507 | NCT03315143 | 2017–2020 | 3 | 10584 |
I: Sotagliflozin C: Placebo |
1.3 years | Reduced risk of cardiovascular-related hospitalization and death from diabetes and CKD, but associated with adverse events. |
VERTIS CV508 | NCT01986881 | 2013–2019 | 3 | 8223 |
I: Ertugliflozin C: Placebo |
3.5 years | Ertugliflozin reduced the risk of composite renal end points and was associated with reduced eGFR and UACR. |
Mineralcorticoid receptor antagonists | |||||||
FIDELIO-DKD191 | NCT02540993 | 2015–2021 | 3 | 5734 |
I: Finerenone C: Placebo |
2.6 years | Reduced the risk of the cardio-renal outcome. |
PRIORITY509 | NCT02040441 | 2014–2018 | 2/3 | 209 |
I: Spironolactone C: Placebo Standard care |
2.5 years | Can’t prevent disease progression of high-risk patients with DKD. |
SONAR510 | NCT01858532 | 2013–2018 | 3 | 2648 |
I: Atrasentan C: Placebo Standard care |
4.4 years | Reduced the risk of renal events in patients with diabetes and CKD. |
Others | |||||||
CKD-FIX181 | ACTRN12611000791932 | 2014–2016 | 3 | 369 |
I: Allopurinol C: Placebo Standard care |
2.17 years | Decreased serum urate but did not affect the renal outcome and did not alleviate the decline in eGFR. |
ALBUM197 | NCT02358096 | 2015–2017 | 2 | 125 |
I:ASP8232 C: Placebo |
2 years | Reduced albuminuria in DKD patients, safe and well tolerated. |
NA196 | NCT01683409 | 2012–2017 | 2 | 130 |
I: Baricitinib C: Placebo |
0.46 years | Reduced albuminuria. |
NA | NCT03804879 | 2018–2021 | 2 | 83 |
I: Nidufexor C: Placebo |
0.54 years | UACR and 24-hour urinary albumin were decreased in DKD patients. |
NA201 | NCT03016832 | 2017–2021 | 1 | 413 |
I: HuangKui capsule C: Irbesartan tablets |
0.46 years | The combination of Huangkui capsule and irbesartan had the best effect on reducing ACR in DKD patients. |
NA no official trial name