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Comparative Bioavailability Study of Two Test Products of Fixed Dose Combination Capsule of ASA (Acetylsalicylic Acid) and Pantoprazole (Each Capsule Contains ASA 100 mg and Pantoprazole 20 mg) Under Fasting Conditions PHASE1 An open label, balanced, randomized, three-treatment, three-period, six-seq...
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GSK Investigational Site
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Randomized, Single-dose, Crossover Study of 4 Decitabine and Tetrahydrouridine (EPI01) Formulations in Healthy Subjects PHASE1 To study the pharmacokinetic profiles of decitabine and tetrahydrouridine (...
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Worldwide Clinical Trial
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Bioavailability of Duloxetine 60 mg With Regards to Reference Product in Fasting Conditions PHASE1 This Study will investigate the bioavailability in fasting subjects of 1 ca...
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To Demonstrate the Relative Bioequivalence of Cefdinir and Omnicef 300 mg Capsule Fasting Conditions PHASE1 To demonstrate the relative bioequivalence of Cefdinir and Omnicel 300 mg c...
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Multiple Locations
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A Bioequivalence Study of SKF101804 Cefixime Versus Cefixime Reference Formulation in Healthy Adults Under Fasting Conditions PHASE1 Cefixime is an orally active third generation cephalosporin indicated for t...
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Multiple Locations
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Evaluating Bioequivalence of a Fixed Dose Combination Versus Individual Tablets of Bempedoic Acid / Ezetimibe, and Atorvastatin PHASE1 Monotherapies for lowering LDL-C often do not achieve target lipid levels b...
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Bioequivalence of Two Fixed-dose Combination Tablets Containing Estradiol and Nomegestrol Acetate PHASE1 This study will investigate the bioavailability in fasting post-menopausal ...
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Investigacíon Farmacológica y Biofarmacéutica (IFaB), S.A.P.I. de C.V.
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A Study to Investigate the Safety, Tolerability, and Pharmacokinetics (PK) of Oral AZD6793 in Healthy and Chronic Obstructive Pulmonary Disease Participants, to Assess the Relative Oral Bioavailability Between Two Formulations, and the Food Effect on the PK of AZD6793 Compared to Fasting State. PHASE1 The purpose of the study is to assess the safety and tolerability of AZD679...
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Single Dose Study With a New Insulin Glargine Formulation and Lantus® in Japanese Patients With Type 1 Diabetes Mellitus PHASE1 Primary Objective:
To compare the pharmacodynamic properties of two differ...
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Investigational Site Number 392001
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A Single Dose Bioequivalence Study Of Neratinib In Healthy Subjects N/A The purpose of the study is to demonstrate the bioequivalence of the propos...
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Investigational Site
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