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Healthy Subjects clinical trials

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NCT ID: NCT01980329 Completed - Healthy Subjects Clinical Trials

Polymorphic Effects of Cytochrome P450 3A5 on Pharmacokinetics of Maraviroc and Its Metabolites

Start date: January 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the influence of genetic polymorphism of cytochrome P450 3A5 on pharmacokinetics of maraviroc and its oxidative metabolites

NCT ID: NCT01959399 Completed - Healthy Subjects Clinical Trials

Drug-Drug Interaction Study Evaluating Effects of ASP015K on Rosuvastatin

Start date: May 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study will be to assess the effect of multiple-doses of ASP015K on the pharmacokinetics of rosuvastatin in healthy adult male and female subjects.

NCT ID: NCT01958645 Completed - Healthy Subjects Clinical Trials

To Assess Safety, Tolerability and Pharmacodynamics of Intravenous MEDI8111 After Single Ascending Doses.

Start date: November 2013
Phase: Phase 1
Study type: Interventional

A study to investigate the safety, tolerability and pharmacodynamics of MEDI8111 after single ascending doses in healthy male.

NCT ID: NCT01958047 Completed - Healthy Subjects Clinical Trials

A Study to Assess the Effect of Race on How a Single Dose of ASP3652 is Taken up, Metabolized and Distributed Through the Bodies of Young, Healthy Male and Female Subjects, and Its Safety and Tolerability

Start date: July 2012
Phase: Phase 1
Study type: Interventional

This study investigates how ASP3652 is taken up, broken down, and distributed through the body and excreted in individuals of different races. The study also investigates levels of biochemical markers in the bloodstream, and determines how safe the study drug is and how well it is tolerated after dosing. A further aim is to look at how the processes of metabolism, distribution and excretion of the study drug are possibly altered by the daily diet of the volunteers taking part.

NCT ID: NCT01955447 Completed - Healthy Subjects Clinical Trials

Post-prandial Glucose in Healthy Subjects

Start date: November 2013
Phase: N/A
Study type: Interventional

The study is designed to determine the extent to which foods containing different levels of plant-based ingredients affect blood glucose responses in healthy subjects.

NCT ID: NCT01953887 Completed - Healthy Subjects Clinical Trials

A Study to Compare the Amount of Drug in the Blood After a Single Tablet EC905 Containing Solifenacin and Tamsulosin is Taken by Healthy Males Compared to Separate Tablets of Solifenacin and Tamsulosin

Start date: March 2010
Phase: Phase 1
Study type: Interventional

A study to assess the amount of drug in the blood of young to middle aged, healthy, male subjects after they received the final formulation of EC905 compared to solifenacin (Vesicare®) and tamsulosin OCAS (Omnic OCAS®). Subjects are given a single dose of the combination tablet EC905, Vesicare® and Omnic OCAS® in 3 separate periods.

NCT ID: NCT01953861 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate Whether Food Has an Effect on the Uptake of Solifenacin and Tamsulosin When Administered in a Combination Tablet

Start date: April 2010
Phase: Phase 1
Study type: Interventional

To evaluate the effect of food (low and high fat breakfast vs. fasting) on the pharmacokinetics (what the body does to the drug) of a single dose of solifenacin and tamsulosin administered as combination tablet EC905. Also to evaluate the safety and tolerability of single doses of EC905 in young, healthy male subjects, when administered under fed (low and high fat) or fasting conditions.

NCT ID: NCT01953848 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate How Tamsulosin (at 1 Dose) and Solifenacin (at 2 Different Doses) Are Taken up From the Intestine, Distributed Through the Body and Eliminated From the Body When Administered in Combination as a Single Tablet (Called EC905)

Start date: April 2010
Phase: Phase 1
Study type: Interventional

Tamsulosin (sold under the name Omnic OCAS) is used for treatment of voiding complaints related to an enlarged prostate. Solifenacin (sold under the name Vesicare) is used for the treatment of patients suffering from problems related to overactive bladder, such as needing to go to the toilet frequently and often having a sudden urgent need to go to the toilet. Certain patients with an enlarged prostate have complaints that may benefit from a combination of tamsulosin and solifenacin. EC905 is a single tablet containing both tamsulosin and solifenacin. The current study aims at investigating how tamsulosin and solifenacin are taken up from the intestine, distributed through the body and eventually eliminated from the body when taken as a single EC905 tablet.

NCT ID: NCT01950988 Terminated - Healthy Subjects Clinical Trials

Effectiveness of a Novel Concept for a Manual Toothbrush Broscyl®

BROSCYL
Start date: July 16, 2013
Phase: N/A
Study type: Interventional

The aim is to determine the efficacy and the satisfaction/adaptability of the manual Broscyl® toothbrush as compared with a standard " soft " manual toothbrush ADA (American Dental Association) reference using the modified Stillman brushing technique, in children, adults and elderly persons, after 3 months of daily use.

NCT ID: NCT01943487 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate Whether Verapamil Has an Effect on the Uptake and Elimination of Solifenacin and Tamsulosin When Administered in a Combination Tablet

Start date: August 2009
Phase: Phase 1
Study type: Interventional

This study investigates the effect of the co-administration of verapamil on the steady-state pharmacokinetics (PK) of solifenacin succinate and tamsulosin given as a combination tablet, EC905.