Oxcarbazepine 600 mg Tablets Under Non-Fasting Conditions The objective of this study is to compare the rate and extent of absorption of a test formulation of oxcarbazepine tablets and Trileptal® tablets administered as a 1 x 600 mg dose under fe...

• Pays Canada
• Organes Aucun
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Losartan 100 mg Tablets in Healthy Subjects Under Fasting Conditions The objective of this study is to compare the rate and extent of absorption of losartan 100 mg tablets (test) versus Cozaar® (reference), administered as 1 * 100 mg tablet under fasting co...

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Single and Multiple Ascending Dose Safety Study of XPF-001 in Healthy Volunteers The purpose of this study is to assess the safety, tolerability and pharmacokinetics of single and multiple doses of XPF-001 in healthy volunteers. The effect of food on the pharmacokinet...

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Bioequivalence Study of Sorafenib Tablet and Nexavar Randomized, open-label, 3-way reference replicated crossover bioequivalence study of sorafenib 200 mg tablet and nexavar (reference) following a 200 mg dose in healthy subjects under fasti...

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Levetiracetam 750 mg Tablets Under Fasting Conditions The objective of this study is to compare the rate and extent of absorption of a test formulation of Levetiracetam and the reference Keppra® administered as a 1 x 750 mg tablet under fasti...

• Pays Canada
• Organes Aucun
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Losartan 100 mg Tablet in Healthy Subjects Under Non-Fasting Conditions The objective of this study is to compare the rate and extent of absorption of losartan 100 mg tablets (test) versus Cozaar® (reference), administered as 1 * 100 mg tablet under fed condit...

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Pharmacokinetic and Pharmacodynamic Study of TH9507, a Growth Hormone-Releasing Factor Analog, in HIV Positive Patients The primary objective of the study is to determine the PK (tesamorelin) and PD (IGF-1) profiles of tesamorelin after a single 2 mg subcutaneous administration and after repeated administra...

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Study of Bicalutamide 1 x 50 mg Tablet in Healthy Subjects Under Fed Conditions The objective of this study is to compare the rate and extent of absorption of bicalutamide 50 mg tablets (test) versus Casodex® (reference) administered as 1 x 50 mg tablet under fed cond...

• Pays Canada
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The Impact of Renal Impairment on the Pharmacokinetic and Pharmacodynamic of LEO 27847 The study will investigate the impact of reduced renal function on the pharmacokinetic and pharmacodynamic profile of LEO 27847. Volunteers with different degrees of renal impairment will ...

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Amoxicillin-Clavulanic Acid 400 mg-57 mg Chewable Tablets Under Non-Fasting Conditions The objective of this study is to compare the rate and extent of absorption of amoxicillin-clavulanic acid 400 mg-57 mg chewable tablets (test) versus Augmentin® (reference) administered a...

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