Source:http://linkedlifedata.com/resource/pubmed/id/21209236
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2011-6-13
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pubmed:abstractText |
This study evaluated the effects of single-dose administration and steady-state concentrations of tipranavir 500 mg and ritonavir 200 mg (TPV/r) combination on the pharmacokinetics of tadalafil 10 mg (TAD) in an open-label study. Seventeen healthy male volunteers received sequential dosing of the studied product: TAD (day 1) alone in a single dose for 7 days followed by TAD (day 8) in a single dose with TPV/r (500/200 mg twice daily, days 8-18). Pharmacokinetic parameters were determined in a noncompartmental analysis. The geometric mean ratio and 90% confidence interval were used to evaluate drug interactions. The effect of a single dose of TAD on the pharmacokinetics of TPV/r resulted in a small decrease in exposure after either first-dose or steady-state TPV/r (geometric mean ratios [90% confidence interval]: area under the concentration-time curve, 0.85 [0.74-0.97]). In contrast, coadministration of TAD exposure was increased significantly (2.33 [2.02-2.69]) when administered with the first dose of TPV/r but not when TPV/r steady state was reached (1.01 [0.83-1.21]). Antiretroviral activity may not be reduced, but the dose of TAD should be reduced at the start of TPV/r therapy and then a full dose can be resumed after steady state is reached.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carbolines,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Protease Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase 5 Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridines,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrones,
http://linkedlifedata.com/resource/pubmed/chemical/Ritonavir,
http://linkedlifedata.com/resource/pubmed/chemical/tadalafil,
http://linkedlifedata.com/resource/pubmed/chemical/tipranavir
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1552-4604
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1071-8
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pubmed:meshHeading |
pubmed-meshheading:21209236-Adult,
pubmed-meshheading:21209236-Biological Availability,
pubmed-meshheading:21209236-Carbolines,
pubmed-meshheading:21209236-Cross-Over Studies,
pubmed-meshheading:21209236-Drug Interactions,
pubmed-meshheading:21209236-HIV Protease Inhibitors,
pubmed-meshheading:21209236-Half-Life,
pubmed-meshheading:21209236-Humans,
pubmed-meshheading:21209236-Male,
pubmed-meshheading:21209236-Metabolic Clearance Rate,
pubmed-meshheading:21209236-Phosphodiesterase 5 Inhibitors,
pubmed-meshheading:21209236-Pyridines,
pubmed-meshheading:21209236-Pyrones,
pubmed-meshheading:21209236-Ritonavir,
pubmed-meshheading:21209236-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Effect of tipranavir/ritonavir combination on the pharmacokinetics of tadalafil in healthy volunteers.
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pubmed:affiliation |
Pharmacology Department, Pasteur University Hospital, Nice, France. garraffo.r@chu-nice.fr
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Controlled Clinical Trial,
Research Support, Non-U.S. Gov't
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