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Updated: Apr 11, 2026

Acute Kidney Injury Model Induced by Cisplatin in Adult Zebrafish
Published on: May 15, 2021
Effects of a DPP4 inhibitor on cisplatin-induced acute kidney injury: study protocol for a randomized controlled
Seon Ha Baek1, Se Hyun Kim2, Jin Won Kim3
1Division of Nephrology, Department of Internal Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam, Gyeonggi-do, 463-707, South Korea. haya2001@hanmail.net.
Background:
Cisplatin is a potent chemotherapeutic agent, but its nephrotoxicity, which results in acute kidney injury (AKI), often limits its clinical application. Although many studies have attempted to target the mechanism responsible for its nephrotoxicity, no such method has been demonstrated to be effective in clinical trials. Recently, a dipeptidyl peptidase-4 (DPP4) inhibitor has been reported to have a renoprotective effect in a mouse model of cisplatin-induced AKI. Therefore, we will evaluate whether a DPP4 inhibitor protects the kidney from cisplatin-induced injury in humans.
Methods/Design:
This is a single-center, prospective, randomized, double-blind, placebo-controlled trial. A total of 182 participants who are scheduled for cisplatin treatment will be enrolled and randomly assigned to receive either a DPP4 inhibitor (gemigliptin) or a placebo. Participants will take the study drugs for 8 days starting 1 day before cisplatin treatment. The primary outcome of interest is the incidence of AKI at 7 days after finishing treatment with cisplatin. The secondary outcomes include changes in serum creatinine levels and estimated glomerular filtration rates from baseline to 7 days after cisplatin treatment.
Discussion:
This is the first clinical trial to investigate the effect of a DPP4 inhibitor on cisplatin-induced AKI.
Trial Registration:
ClinicalTrials.gov number NCT02250872, December 26, 2014.
Insights
This study investigates if gemigliptin, a dipeptidyl peptidase-4 (DPP4) inhibitor, can prevent acute kidney injury (AKI) caused by cisplatin chemotherapy in humans. The trial aims to determine the drug
Area of Science:
- Nephrology
- Oncology
- Pharmacology
Background:
- Cisplatin chemotherapy can cause significant kidney damage, known as acute kidney injury (AKI), limiting its use.
- Previous research in mice suggested that dipeptidyl peptidase-4 (DPP4) inhibitors may protect the kidneys from cisplatin-induced damage.
- No effective clinical interventions currently exist to prevent cisplatin-induced nephrotoxicity.
Purpose of the Study:
- To evaluate the efficacy of a DPP4 inhibitor, gemigliptin, in preventing cisplatin-induced AKI in human patients.
- To assess the renoprotective effects of gemigliptin in the context of cancer chemotherapy.
Main Methods:
- A single-center, prospective, randomized, double-blind, placebo-controlled trial involving 182 participants.
- Participants received either gemigliptin or a placebo for 8 days, starting one day before cisplatin treatment.
- Primary outcome: incidence of AKI at 7 days post-treatment. Secondary outcomes: changes in serum creatinine and estimated glomerular filtration rate.
Main Results:
- The study is the first clinical trial to examine the effect of a DPP4 inhibitor on cisplatin-induced AKI.
- Results regarding the incidence of AKI and changes in renal function markers are pending analysis.
Conclusions:
- This trial represents a novel investigation into a potential therapeutic strategy for mitigating chemotherapy-induced kidney damage.
- Findings will inform future clinical practice regarding the use of DPP4 inhibitors in patients undergoing cisplatin treatment.
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Acute Kidney Injury II: Pathophysiology
Dipeptidyl Peptidase 4 Inhibitors
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Acute Kidney Injury V: Interprofessional Care

