Exposure-QT analysis for sonidegib (LDE225), an oral inhibitor of the hedgehog signaling pathway, for measures of the QT prolongation potential in healthy subjects and in patients with advanced solid tumors
Autor: | Dalila Sellami, Eunju Hurh, Jocelyn Zhou, Michelle Quinlan |
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Rok vydání: | 2016 |
Předmět: |
Adult
Male 0301 basic medicine medicine.medical_specialty Pyridines Antineoplastic Agents Torsades de pointes QT interval Sonidegib Electrocardiography 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Heart Rate Neoplasms Internal medicine Heart rate medicine Humans Hedgehog Proteins Pharmacology (medical) Pharmacology medicine.diagnostic_test business.industry Biphenyl Compounds Prolongation General Medicine Middle Aged medicine.disease Healthy Volunteers Confidence interval Biphenyl compound 030104 developmental biology chemistry 030220 oncology & carcinogenesis Anesthesia Cardiology Female business Signal Transduction |
Zdroj: | European Journal of Clinical Pharmacology. 72:1427-1432 |
ISSN: | 1432-1041 0031-6970 |
DOI: | 10.1007/s00228-016-2128-8 |
Popis: | Sonidegib prevents activation of the Hedgehog signal transduction pathway. This PK-QT analysis has been performed to test for potential prolongation of the QT/QTc interval during extended use, and to understand the exposure-QT relationship for sonidegib in patients and in healthy volunteers (HV). A pooled analysis of the change in QT interval corrected for heart rate according to Fridericia’s formula was conducted across four patient studies from a total of 341 patients (n = 211, 102, 21, and 7 from the phase II pivotal study A2201, study X2101, study X1101, and study B2209, respectively), and across four healthy volunteer studies from a total of 204 healthy volunteers (n = 146, 36, 16, and 6 from study A2114, study A1102, study A2108, and study A2110, respectively). A PK/ECG subgroup of 62 patients from the pivotal study A2201 was also analyzed to assess the QT prolongation risk at steady-state exposures. Sonidigib PK and ECG data were matched to determine the change from baseline in QTcF using a linear mixed-effect model. Clinical data indicate sonidegib does not cause QTc prolongation. ΔQTcF at steady-state concentrations for both 200 and 800-mg doses were all below 5 ms. The highest mean ΔQTcF at steady state was −3.9 ms at week 17 pre-dose in the sonidegib 200-mg group and 2.7 ms at 2-h post-dose in the sonidegib 800-mg group. The upper one-sided 95 % confidence interval of the estimated ΔQTcF at steady-state concentrations from the linear mixed-effect models were all |
Databáze: | OpenAIRE |
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