Found 116 matching trials
Bioequivalence Study of Metformin Component of Fixed Dose Combination (FDC) Immediate Release (IR) Tablet of Canagliflozin and Metformin Compared to Metformin IR Tablet Co-administered With Canagliflozin in Healthy Fed and Fasted Participants PHASE1 The purpose of this study is to evaluate the bioequivalence of metformin co...
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Multiple Locations
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Bioequivalence Study for Acarbose / Metformin FDC PHASE1 To establish the bioequivalence between Acarbose / Metformin FDC (50mg / 50...
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Multiple Locations
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Glyburide/Metformin 5 mg/500 mg Film-Coated Tablets, Fed PHASE1 The objective of this study is to compare the rate and extent of absorption...
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Dose Proportionality Study About Amaryl M Slow Release (SR) 1/500 mg PHASE1 The pharmacokinetics of glimepiride and metformin will be compared after si...
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Seoul National University Hospital
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Bioequivalence Study of Sitagliptin/Metformin Extended-Release Tablets in Healthy Subjects PHASE1 The main purpose of this study is to compare the pharmacokinetics (how the ...
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The Affiliated Hospital of Qingdao University
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Study in Healthy Subjects to Measure Amount of Drug in Blood After Dosing With Different Saxagliptin / Metformin Produc PHASE1 Study in healthy subjects to measure amount of drug in blood after dosing w...
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Fed Bioequivalence Study of 2 Metformin 500 mg Prolongued Release Tablets in 28 Healthy Male and Female Volunteers PHASE1 The objective of the study is to compare the bioavailability of the Test an...
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QUINTA-ANALYTICA s.r.o.
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Glucophage Immediate Release (GIR) China Bioequivalence Study PHASE1 The study will assess the bioequivalence between single doses of glucophage...
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Bioequivalence Study in Healthy Volunteers for Empagliflozin/Metformin Fixed Dose Combination Compared to Separate Tablets PHASE1 The trial is being conducted to establish the bioequivalence of emp/met (12...
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1276.24.001 Boehringer Ingelheim Investigational Site
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A Bioequivalence Study of the Fixed Dose Combinations of Saxagliptin/Metformin XR Relative to Co-Administration PHASE1 The primary objective of this study is to assess the pharmacokinetic parame...
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