AI Article Synopsis

  • Belumosudil is a selective inhibitor tested in a study with 34 subjects to evaluate its effects on heart function using electrocardiograms (ECGs).
  • The study found that neither therapeutic (200 mg) nor supratherapeutic (1000 mg) doses of belumosudil caused significant changes in the QTc interval, a measure of heart rhythm, with any changes being less than 10 milliseconds.
  • Overall, the results showed no clinically relevant impact on heart rate or conduction, confirming that belumosudil is safe in terms of ECG parameters.

Article Abstract

Belumosudil is a selective Rho-associated, coiled-coil-containing protein kinase-2 inhibitor. In this crossover design thorough QT/QTc study, single therapeutic (200 mg) and supratherapeutic (1000 mg) oral doses of belumosudil, moxifloxacin (positive control), and placebo were administered to 34 subjects. Twelve-lead electrocardiograms and serial pharmacokinetic sampling were acquired. The effect of belumosudil on the placebo-corrected, change-from-baseline QTcF was small, and an effect exceeding 10 ms could be excluded across all time points with both doses. Using concentration-QTc analysis, an effect on ΔΔQTcF >10 ms can be excluded up to belumosudil concentrations of ≈12 080 ng/mL, more than 2-fold above mean C after the supratherapeutic dose. There was no clinically relevant effect on heart rate or cardiac conduction (ie, the PR and QRS intervals) for belumosudil. No differences in safety were noted between belumosudil and placebo treatment. Assay sensitivity was demonstrated by moxifloxacin's effect on the QTc interval. In conclusion, belumosudil at therapeutic and supratherapeutic doses did not have a clinically meaningful effect on electrocardiogram parameters.

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Source
http://dx.doi.org/10.1002/cpdd.1142DOI Listing

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