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16th International AIDS ConferenceToronto, Canada - August 13 - 18, 2006 |
OVERVIEW OF DRUG INTERACTIONS BETWEEN BRECANAVIR (BCV) AND OTHER HIV PROTEASE INHIBITORS (PIS)
Int Conf AIDS. 2006 Aug 13-18;16 Abstract No. TuAb0105
M.J. Shelton, S. Ford, M.T. Anderson, S. Murray, J. Ng-Cashin
GlaxoSmithKline, Research Triangle Park, United States
BACKGROUND: BCV is a potent PI, currently in Phase II development. Chronic doses of BCV (150mg, 300mg, and 600mg)/RTV 100mg q12h are currently under investigation in treatment-experienced HIV patients. An overview of BCV drug interactions with other RTV-boosted PIs is provided.
METHODS: Three multiple-dose drug interaction studies were conducted in healthy adults. In Study 1, BCV 300mg q12h was administered with lopinavir/ritonavir (LPV/r) 400mg/100mg q12h and compared to BCV 300mg/RTV 100mg q12h or LPV/r q12h. In Study 2, BCV 300mg/RTV 100mg q12h was administered with atazanavir (ATV) 300mg q24h and compared to BCV 300mg/RTV 100mg q12h or ATV 300mg/RTV 100mg q24h. In Study 3, BCV 600mg/RTV 100mg q12h was given alone in Period 1, followed by BCV 600mg/RTV 200mg q12h or BCV 600mg/RTV 200mg + tipranavir (TPV) 500mg q12h in Period 2. Plasma concentrations of PIs were determined by LC/MS/MS and PK parameters were compared by ANOVA.
RESULTS: Change in PK parameters for BCV/PI combinations In Study 3, combination dosing of BCV/RTV + TPV was discontinued prior to collection of steady-state pharmacokinetic data due to asymptomatic hepatic transaminase elevations (all Grades 1 – 2, except one subject with Grade 3 – 4). All elevations returned to baseline after discontinuation of study drugs.
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| Study | Analyte | AUC(0–τ) | Cmax | Cτ | |
| 1 | BCV | ↓16% ↓7–25% | ↔ | ↓16% ↑2–↓17% | |
| 1 | LPV | ↔ | ↔ | ↔ | |
| 2 | BCV | ↑38% (↑25–53%) | ↑48% (↑29–71%) | ↑44% (↑25–65%) | |
| 2 | ATV | ↑44% (↑32–58%) | ↑21% (↑12–30%) | ↑111% (↑81–145%) | |
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CONCLUSIONS: BCV exposure was slightly reduced and LPV was unaffected following coadministration with LPV/r. Exposure to both BCV and ATV were increased following coadministration with ATV/RTV. BCV should not be coadministered with TPV/RTV. BCV appears to have a generally favorable drug interaction profile with LPV/r and ATV, such that significant reductions in plasma exposure are not apparent.
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2006-08-13
TuAb0105
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