Key result
Teprasiran reduces postoperative AKI ~42% vs. placebo in high-risk cardiac surgery.
Why the study?
Does a single dose of teprasiran reduce the incidence of acute kidney injury in high-risk patients undergoing cardiac surgery?
RCT
Double-blind
1:1
Yes
Does a single dose of teprasiran reduce the incidence of acute kidney injury in high-risk patients undergoing cardiac surgery?
Odds Ratio: 0.58 (95% CI 0.37–0.92)
p-value: p=0.02
A single dose of teprasiran significantly reduced the incidence, severity, and duration of early acute kidney injury in high-risk patients undergoing cardiac surgery.
BACKGROUND: Acute kidney injury (AKI) affects up to 30% of patients undergoing cardiac surgery, leading to increased in-hospital and long-term morbidity and mortality. Teprasiran is a novel small interfering RNA that temporarily inhibits p53-mediated cell death that underlies AKI. METHODS: This prospective, multicenter, double-blind, randomized, controlled phase 2 trial evaluated the efficacy and safety of a single 10 mg/kg dose of teprasiran versus placebo (1:1), in reducing the incidence, severity, and duration of AKI after cardiac surgery in high-risk patients. The primary end point was the proportion of patients who developed AKI determined by serum creatinine by postoperative day 5. Other end points included AKI severity and duration using various prespecified criteria. To inform future clinical development, a composite end point of major adverse kidney events at day 90, including death, renal replacement therapy, and ≥25% reduction of estimated glomerular filtration rate was assessed. Both serum creatinine and serum cystatin-C were used for estimated glomerular filtration rate assessments. RESULTS: =0.02; odds ratio, 0.58 (95% CI, 0.37-0.92). AKI severity and duration were also improved with teprasiran: 2.5% of teprasiran- versus 6.7% of placebo-treated patients had grade 3 AKI; 7% teprasiran- versus 13% placebo-treated patients had AKI lasting for 5 days. No significant difference was observed for the major adverse kidney events at day 90 composite in the overall population. No safety issues were identified with teprasiran treatment. CONCLUSIONS: The incidence, severity, and duration of early AKI in high-risk patients undergoing cardiac surgery were significantly reduced after teprasiran administration. A phase 3 study with a major adverse kidney event at day 90 primary outcome that has recently completed enrollment was designed on the basis of these findings (NCT03510897). Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02610283.
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Thielmann et al. (2021) conducted an RCT in Acute kidney injury (AKI). Teprasiran vs. placebo was evaluated on proportion of patients who developed AKI determined by serum creatinine by postoperative day 5 (OR 0.58, 95% CI 0.37-0.92, p=0.02). Teprasiran significantly reduced the incidence of acute kidney injury by postoperative day 5 compared to placebo in high-risk patients undergoing cardiac surgery (OR 0.58; 95% CI 0.37-0.92; P=0.02).