Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
J Cardiovasc Pharmacol ; 61(1): 83-9, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23107871

ABSTRACT

INTRODUCTION: Vismodegib was assessed as being of low risk for QT interval prolongation based on prior nonclinical and clinical experience. A dedicated study was conducted to further assess the potential for vismodegib to prolong the QTc interval. METHODS AND RESULTS: Given the nonlinear pharmacokinetics of vismodegib, a thorough QTc study as is typically designed was not possible, and an innovative design was employed. This dedicated QTc study was powered to exclude a 20-millisecond change from the baseline QTc interval. The subjects were administered daily oral 150 mg of vismodegib for 7 days, or a single dose of 400 mg of moxifloxacin, with corresponding matching placebos. The upper limits of the 90% confidence intervals for the difference in ΔQTcF between vismodegib and placebo at steady state were <20 milliseconds at all timepoints with a maximum of 10 milliseconds at 12 hours postdose. Exposure-response analysis yielded an estimated slope equal to 0.11 ms/µM, which was not statistically significant. After a single dose of moxifloxacin was administered, the lower limits of the 90% confidence interval of the difference in ΔQTcF between moxifloxacin and placebo were >5 milliseconds from 1-12 hours postdose, thereby establishing assay sensitivity. CONCLUSIONS: There was no effect of vismodegib on the QTc interval when dosed daily at 150 mg to steady state.


Subject(s)
Anilides/administration & dosage , Antineoplastic Agents/administration & dosage , Pyridines/administration & dosage , Administration, Oral , Aged , Anilides/adverse effects , Anilides/pharmacokinetics , Antineoplastic Agents/adverse effects , Antineoplastic Agents/pharmacokinetics , Aza Compounds/administration & dosage , Double-Blind Method , Drug Administration Schedule , Electrocardiography , Female , Fluoroquinolones , France , Heart Rate/drug effects , Humans , Linear Models , Long QT Syndrome/chemically induced , Long QT Syndrome/physiopathology , Middle Aged , Models, Biological , Moxifloxacin , Pyridines/adverse effects , Pyridines/pharmacokinetics , Quinolines/administration & dosage , Risk Assessment , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...