Persistence of a Posaconazole-Mediated Drug-Drug Interaction With Ranolazine After Cessation of Posaconazole Administration: Impact of Obesity and Implications for Patient Safety
The antianginal agent ranolazine (Ranexa®) is metabolized primarily by cytochrome P450-3A (CYP3A) enzymes. Coadministration with strong CYP3A inhibitors, such as ketoconazole and posaconazole, is contraindicated due to risk of QT prolongation from high levels of ranolazine. This study evaluated the...
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Published in | Journal of clinical pharmacology Vol. 58; no. 11; p. 1436 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
01.11.2018
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Subjects | |
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Abstract | The antianginal agent ranolazine (Ranexa®) is metabolized primarily by cytochrome P450-3A (CYP3A) enzymes. Coadministration with strong CYP3A inhibitors, such as ketoconazole and posaconazole, is contraindicated due to risk of QT prolongation from high levels of ranolazine. This study evaluated the time course of recovery from the posaconazole drug interaction in normal-weight and otherwise healthy obese subjects. Subjects received single doses of ranolazine in the baseline control condition, again during coadministration of posaconazole, and at 4 additional time points during the 2 weeks after posaconazole discontinuation. With posaconazole coadministration, the geometric mean ratio of ranolazine area under the concentration curve (AUC) increased by a factor of 3.9 in normals and by 2.8 in obese subjects. Posttreatment washout of posaconazole was slow in normals (mean half-life 36 hours) and further prolonged in obese subjects (64 hours). Recovery of ranolazine AUC toward baseline was delayed. AUC remained significantly elevated above baseline in normal-weight and obese subjects for 7-14 days after stopping posaconazole. Current product labeling does not address the need for delay or a reduced dose of ranolazine after discontinuation of a strong CYP3A inhibitor before ranolazine can be safely administered. We recommend that administration of ranolazine should be limited to 500 mg twice daily for 7 days after posaconazole discontinuation in patients with body mass index 18.5-24.9 kg/m
and for 12 days in patients with body mass index ≥35 kg/m
after ranolazine is resumed. |
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AbstractList | The antianginal agent ranolazine (Ranexa®) is metabolized primarily by cytochrome P450-3A (CYP3A) enzymes. Coadministration with strong CYP3A inhibitors, such as ketoconazole and posaconazole, is contraindicated due to risk of QT prolongation from high levels of ranolazine. This study evaluated the time course of recovery from the posaconazole drug interaction in normal-weight and otherwise healthy obese subjects. Subjects received single doses of ranolazine in the baseline control condition, again during coadministration of posaconazole, and at 4 additional time points during the 2 weeks after posaconazole discontinuation. With posaconazole coadministration, the geometric mean ratio of ranolazine area under the concentration curve (AUC) increased by a factor of 3.9 in normals and by 2.8 in obese subjects. Posttreatment washout of posaconazole was slow in normals (mean half-life 36 hours) and further prolonged in obese subjects (64 hours). Recovery of ranolazine AUC toward baseline was delayed. AUC remained significantly elevated above baseline in normal-weight and obese subjects for 7-14 days after stopping posaconazole. Current product labeling does not address the need for delay or a reduced dose of ranolazine after discontinuation of a strong CYP3A inhibitor before ranolazine can be safely administered. We recommend that administration of ranolazine should be limited to 500 mg twice daily for 7 days after posaconazole discontinuation in patients with body mass index 18.5-24.9 kg/m
and for 12 days in patients with body mass index ≥35 kg/m
after ranolazine is resumed. |
Author | Harmatz, Jerold S Ryan, Michael J Greenblatt, David J Chow, Christina R |
Author_xml | – sequence: 1 givenname: Christina R orcidid: 0000-0003-3944-4234 surname: Chow fullname: Chow, Christina R organization: Emerald Lake Safety LLC, Newport Beach, CA, USA – sequence: 2 givenname: Jerold S surname: Harmatz fullname: Harmatz, Jerold S organization: Tufts University School of Medicine, Boston, MA, USA – sequence: 3 givenname: Michael J surname: Ryan fullname: Ryan, Michael J organization: Emerald Lake Safety LLC, Newport Beach, CA, USA – sequence: 4 givenname: David J surname: Greenblatt fullname: Greenblatt, David J organization: Tufts University School of Medicine, Boston, MA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29749631$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1002_jcph_1622 crossref_primary_10_1002_cpdd_636 crossref_primary_10_1002_jcph_2306 crossref_primary_10_1002_jcph_2093 crossref_primary_10_1097_FTD_0000000000000952 crossref_primary_10_1111_bcp_14735 crossref_primary_10_1007_s40265_020_01306_y crossref_primary_10_1007_s13679_023_00532_1 crossref_primary_10_1134_S0022476619070205 crossref_primary_10_1002_jcph_2308 crossref_primary_10_3390_pharmaceutics14040789 crossref_primary_10_1002_jcph_1947 |
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Keywords | posaconazole CYP3A ranolazine QT prolongation drug-drug interaction obesity |
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Snippet | The antianginal agent ranolazine (Ranexa®) is metabolized primarily by cytochrome P450-3A (CYP3A) enzymes. Coadministration with strong CYP3A inhibitors, such... |
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Title | Persistence of a Posaconazole-Mediated Drug-Drug Interaction With Ranolazine After Cessation of Posaconazole Administration: Impact of Obesity and Implications for Patient Safety |
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