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Published in 2022 at "Clinical Pharmacology in Drug Development"
DOI: 10.1002/cpdd.1126
Abstract: Sulfobutyl ether‐beta‐cyclodextrin sodium salt contained in the marketed intravenous voriconazole injection as a solubilizer may cause harmful accumulations. This study aimed to evaluate the safety, tolerability, and pharmacokinetics (PKs) of two intravenous voriconazole formulations containing…
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Keywords:
safety;
two intravenous;
chinese volunteers;
dose administrations ... See more keywords
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Published in 2022 at "Clinical Pharmacology in Drug Development"
DOI: 10.1002/cpdd.1157
Abstract: To assess the bioequivalence of a generic safinamide tablet (test) vs a brand‐name safinamide tablet (reference) and effects of food on the pharmacokinetics of safinamide in healthy Chinese subjects, a single‐center, single‐dose, randomized, open‐label, 2‐preparation,…
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Keywords:
time;
fasting fed;
chinese volunteers;
fed conditions ... See more keywords
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Published in 2023 at "Clinical Pharmacology in Drug Development"
DOI: 10.1002/cpdd.1229
Abstract: Lopinavir/ritonavir is an important protease inhibitor for treating HIV‐1 infection in patients aged >2 years in combination with other antiretrovirals. The antiviral activity of lopinavir/ritonavir in vivo is mainly derived from lopinavir, while ritonavir improves…
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Keywords:
chinese volunteers;
bioequivalence;
lopinavir ritonavir;
healthy chinese ... See more keywords
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Published in 2017 at "International journal of clinical pharmacology and therapeutics"
DOI: 10.5414/cp202762
Abstract: PURPOSE To develop a sensitive, two-dimensional liquid chromatography (2D-LC) method for determination of valsartan, applied to investigate bioequivalence of two valsartan tablets in Chinese volunteers under fasting condition. METHODS A full automatic 2D-HPLC system was…
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Keywords:
bioequivalence;
hplc;
valsartan;
bioequivalence study ... See more keywords