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To Determine the Bioequivalence Study Under Fed
Clinical trial pipeline · Data from ClinicalTrials.gov
See which To Determine the Bioequivalence Study Under Fed trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which To Determine the Bioequivalence Study Under Fed trials you may qualify forComparative, Randomized, Single Dose, Two-way Crossover Bioequivalence Study to determine the bioequivalence of Metformin HCl From Gleptomet 50/1000 mg F.C.Tabl…
The purpose on this study was to determine whether the test product, Haloperidol Tablets, 2 mg (Cycle Pharmaceuticals Ltd), and the reference product, Haloperid…
To evaluate and compare the relative bioavailability and therefore the bioequivalence of fixed dose combination of Metformin and Vildagliptin Tablets 850/50 mg…
To evaluate and compare the relative bioavailability and therefore the bioequivalence of fixed dose combination of Metformin and Vildagliptin Tablets 1000/50 mg…
Two tamsulosin HClformulations will be tested in fed state
In Brazil, duloxetine is currently available as hard gelatinous capsule with delayed release microgranules for oral administration containing enteric-coated pel…
This is an open-label, randomized, single dose, two-sequence, two-periods crossover study, separated by 7 days washout interval from the first Study Drug Admini…
To compare the relative bioavailability of Kali and Ortho-McNeil's products
To compare the single-dose Bioavailability of Kali and Aventis
The purpose of this study is to compare the single-dose Bioavailability of Kali and G.D. Searle, Inc.