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Healthy Subjects clinical trials

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NCT ID: NCT01611428 Completed - Healthy Subjects Clinical Trials

Absolute Bioavailability Study With Ipragliflozin

Start date: June 2011
Phase: Phase 1
Study type: Interventional

A study to assess the absolute bioavailability of ipragliflozin in healthy subjects.

NCT ID: NCT01611415 Completed - Healthy Subjects Clinical Trials

Drug to Drug Interaction Study With Ipragliflozin and Furosemide

Start date: July 2011
Phase: Phase 1
Study type: Interventional

A study to investigate if there are any pharmacodynamic and pharmacokinetic interactions between furosemide and ipragliflozin (ASP1941) in healthy volunteers.

NCT ID: NCT01590667 Completed - Healthy Subjects Clinical Trials

Effect of Litramine on Fat Excretion

Start date: May 2012
Phase: Phase 4
Study type: Interventional

The study aims to evaluate the effect of Litramine on fecal fat excretion in healthy subjects, to provide more comprehensive and robust clinical evidence in its mode of action for the treatment of obesity and weight management through dietary fat binding.

NCT ID: NCT01590368 Unknown status - Healthy Subjects Clinical Trials

A Comparative Wear Test of Two Adhesives on the Unilect ™ Biotab Short Term Monitoring Electrode

Start date: June 2012
Phase: Phase 3
Study type: Interventional

It is hypothesised that the adhesion of electrodes and acceptability of the Electrocardiogram (ECG) trace is comparable between the two groups (marketed and test products) after 30 minutes (the intended period of use) of the electrodes.

NCT ID: NCT01579461 Completed - Healthy Subjects Clinical Trials

A Study to Investigate the Effect of Mirabegron (YM178) on Subjects With Mild or Moderate Hepatic Impairment Compared to Healthy Subjects

Start date: November 2008
Phase: Phase 1
Study type: Interventional

The study aims to investigate and compare the effect of Mirabegron (YM178) on subjects with mild and moderate hepatic impairment compared to healthy subjects.

NCT ID: NCT01577459 Completed - Healthy Subjects Clinical Trials

A Phase 1 Crossover Study of Blood Pressure and Heart Rate Response

Start date: April 23, 2012
Phase: Phase 1
Study type: Interventional

This is a randomized, double-blinded, placebo-controlled, crossover study to evaluate the pressor effects of pseudoephedrine when administered with TR-701 FA in healthy adult volunteers.

NCT ID: NCT01571921 Completed - Healthy Subjects Clinical Trials

Gamma-delta Tocotrienol as Potential Maintenance Treatment in Women With Metastatic Breast Cancer

GEMM1a
Start date: January 2013
Phase: Phase 1
Study type: Interventional

Twelve healthy volunteers who fit the inclusion and exclusion criteria and provide written informed consent to participate in the trial will be recruited to compare the rate and extent of absorption and pharmacokinetics of the newly formulated Gamma-Delta formulation with TRF.

NCT ID: NCT01568697 Recruiting - Healthy Subjects Clinical Trials

Oral Bacteria and Immune System Problems Involved in Gum Disease (Periodontitis)

Start date: October 5, 2012
Phase:
Study type: Observational

Background: - Gum disease is a condition in which the tissue around the tooth root becomes swollen and infected. This condition can cause tooth loss if it is not treated. Who gets gum disease and how bad it will be depends on (1) the different bacteria in the mouth and (2) how the immune system of an individual handles these bacteria. Researchers want to look at the oral bacteria and genetic immune problems of different people to learn how these affect gum disease and other conditions of the mouth. Objectives: - To study how immune system problems may lead to problems in the mouth, including gum disease. Eligibility: - Children and adults at least 7 years of age who have genetic problems with their immune system. - Healthy adults that have periodontal disease - Health adults that do not have periodontal disease Design: - This study will involve a screening visit and a study visit. - Participants will be screened with a medical history, blood work and a full oral and dental exam, including dental x-rays and photos. - The study visit will involve collection of blood, urine, and other samples, including saliva, plaque, and gum swabs. Any abnormal tissue will sampled for a biopsy. Additional oral and dental exams will be performed. Participants will also answer questions about any current medical or dental problems.

NCT ID: NCT01566825 Completed - Healthy Subjects Clinical Trials

The Influence of Amitriptyline on Learning in a Visual Discrimination Task

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether 75 mg amitriptyline affect the sleep dependent consolidation of procedural memory (visual discrimination task, Karni-Sagi-paradigm).

NCT ID: NCT01561963 Completed - Healthy Subjects Clinical Trials

A Drug-Drug Interaction Study to Evaluate the Effect of Rifampin on the Pharmacokinetics of Apremilast

Start date: February 1, 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate how the pharmacokinetics of apremilast may be affected by a single intravenous dose of rifampin and multiple oral doses of rifampin.