Proarrhythmic safety of repeat doses of mirabegron in healthy subjects: a randomized, double‐blind, placebo‐, and active‐controlled thorough QT study

M Malik, EM Van Gelderen, JH Lee… - Clinical …, 2012 - Wiley Online Library
M Malik, EM Van Gelderen, JH Lee, DL Kowalski, M Yen, R Goldwater, SK Mujais…
Clinical Pharmacology & Therapeutics, 2012Wiley Online Library
Potential effects of the selective β3‐adrenoceptor agonist mirabegron on cardiac
repolarization were studied in healthy subjects. The four‐arm, parallel, two‐way crossover
study was double‐blind and placebo‐and active (moxifloxacin)‐controlled. After 2 baseline
ECG days, subjects were randomized to one of eight treatment sequences (22 females and
22 males per sequence) of placebo crossed over with once‐daily (10 days) 50, 100, or 200
mg mirabegron or a single 400‐mg moxifloxacin dose on day 10. In each period, continuous …
Potential effects of the selective β3‐adrenoceptor agonist mirabegron on cardiac repolarization were studied in healthy subjects. The four‐arm, parallel, two‐way crossover study was double‐blind and placebo‐ and active (moxifloxacin)‐controlled. After 2 baseline ECG days, subjects were randomized to one of eight treatment sequences (22 females and 22 males per sequence) of placebo crossed over with once‐daily (10 days) 50, 100, or 200 mg mirabegron or a single 400‐mg moxifloxacin dose on day 10. In each period, continuous ECGs were recorded at two baselines and on the last drug administration day. The lower one‐sided 95% confidence interval for moxifloxacin effect on QTcI was >5 ms, demonstrating assay sensitivity. According to ICH E14 criteria, mirabegron did not cause QTcI prolongation at the 50‐mg therapeutic and 100‐mg supratherapeutic doses in either sex. Mirabegron prolonged QTcI interval at the 200‐mg supratherapeutic dose (upper one‐sided 95% CI >10 ms) in females, but not in males.
Clinical Pharmacology & Therapeutics (2012); 92 6, 696–706. doi:10.1038/clpt.2012.181
Wiley Online Library