Why the study?
Peramivir was reported to induce QT-interval prolongation in some phase III studies despite a negative thorough QT/QTc study, leaving this clinical discrepancy unexplained.
Does intravenous peramivir prolong the QT interval and delay ventricular repolarization in an isoflurane-anesthetized dog model?
Does intravenous peramivir prolong the QT interval and delay ventricular repolarization in an isoflurane-anesthetized dog model?
Peramivir delays ventricular repolarization in vivo, supporting clinical observations of QT prolongation and highlighting the need for caution in patients predisposed to torsade de pointes.
Suggests a mechanistic basis for peramivir-induced QT prolongation; supports clinical caution in patients at.
An injectable anti-influenza drug peramivir has been reported to induce QT-interval prolongation in some phase III studies, although its thorough QT/QTc study was negative. We investigated the discrepancy among those clinical studies using isoflurane-anesthetized beagle dogs (n = 4). Peramivir in doses of 1 mg/kg/10 min (sub-therapeutic dose) followed by 10 mg/kg/10 min (clinically-relevant dose) was intravenously administered. Peramivir prolonged QT interval/QTcV and Tpeak-Tend, and tended to delay ventricular repolarization with reverse-frequency dependency, indicating IKr inhibition in vivo. Meanwhile, peramivir did not alter P-wave duration, PR interval or QRS width, indicating a lack of impact on cardiac conduction via Na + or Ca2+ channel inhibition in vivo. Peramivir prolonged Tpeak-Tend and tended to prolong terminal repolarization period, which would develop substrates for initiating and maintaining spiral reentry, respectively. Meanwhile, peramivir did not prolong J-Tpeakc, which could not induce early afterdepolarization, a trigger inducing torsade de pointes. Thus, our results support that clinical dose exposure of peramivir can delay the ventricular repolarization in influenza patients. Peramivir has a small potential to induce torsade de pointes in patients with the intact hearts, but caution should be paid on its use for patients formerly having the trigger for torsade de pointes.
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Kambayashi et al. (2024) studied this question.
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