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A Phase I, Open Label, Randomized, Single Dose, Crossover Study in Healthy Subjects to Compare the Oral Bioavailability of a Prototype Tablet Formulation of Darunavir 800mg(G002) to That of the Commercial 400mg(F030) Tablet Formulation Under Fed & Fasted Conditions, in Presence of Low-dose Ritonavir
Conditions
Interventions
DRV commercial formulation/ DRV new formulation/ rtv 100mg tab
DRV commercial formulation/ DRV new formulation/ rtv 100mg tab
+2 more
Start Date
March 1, 2010
Primary Completion Date
June 1, 2010
Completion Date
July 1, 2010
Last Updated
September 4, 2013
NCT04142047
NCT06694805
NCT07428330
NCT07225530
NCT05897099
NCT06665646
Lead Sponsor
Tibotec Pharmaceuticals, Ireland
Data Source & Attribution
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