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Healthy Volunteers clinical trials

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NCT ID: NCT02278393 Completed - Healthy Volunteers Clinical Trials

A Clinical Study for Evaluating the Safety of a Plant Sterol-enriched Fermented Dairy Product in Japanese Healthy Adults

Start date: February 2014
Phase: N/A
Study type: Interventional

Investigate the safety of excessive consumption of plant sterol-enriched fermented dairy product over a 4-week period in Japanese healthy adults

NCT ID: NCT02271425 Completed - Healthy Volunteers Clinical Trials

A Study to Measure the Amount of Evacetrapib That Enters the Blood Stream in Healthy Participants

Start date: October 2014
Phase: Phase 1
Study type: Interventional

Evacetrapib (study drug) is an investigational drug being developed with the aim to help people at high risk of heart problems in the future. In this study we will be comparing how much of the study drug gets into the blood stream when it is given as a single dose (in tablet form) compared to an intravenous injection (given directly into a vein via a small needle). The study is expected to last at least 15 days for each participant, not including screening. Screening will occur up to 28 days before the study drug is given.

NCT ID: NCT02271113 Completed - Healthy Volunteers Clinical Trials

Phase I Study to Assess Safety and Pharmacokinetics of GMI-1271 in Healthy Adult Subjects

Start date: October 2014
Phase: Phase 1
Study type: Interventional

In this study, the investigators will evaluate the safety, pharmacokinetics and effect on target biomarkers of coagulation, cell adhesion, and leukocyte and platelet activation of GMI-1271, an E-selectin antagonist, in healthy volunteers.

NCT ID: NCT02268838 Completed - Healthy Volunteers Clinical Trials

Single/ Multiple-Dose Study of E6007 in Healthy Japanese Male Subjects

Start date: October 2014
Phase: Phase 1
Study type: Interventional

This is a single-center, placebo-controlled, randomized, ascending dose, double-blind study. This study will be evaluating ascending doses of 50, 100, 200, and 400 mg of E6007. This study consists of 5 steps, 1 to 5. In steps 1 to 4 (at ascending doses of 50, 100, 200, and 400 mg), subjects will be randomly assigned in a 6:2 ratio (E6007: placebo) to receive single dose of the study drug under fasted condition. Following 3 days of washout period, subject will receive the study drug once daily for 7 days starting on the fifth day from the single dose administration. For step 3 (200 mg), subjects will subsequently have at least 17 days of washout period before being escalated to step 5 (200 mg) to receive single dose of E6007 under fed condition, to evaluate food effect of the study drug.

NCT ID: NCT02265783 Completed - Healthy Volunteers Clinical Trials

Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable

Start date: September 2014
Phase: N/A
Study type: Observational

The purpose of this study is to validate that the device posts a Sensor-Off message within the time frame stated in the proposed claims.

NCT ID: NCT02263911 Completed - Healthy Volunteers Clinical Trials

A Study of Baricitinib in Healthy Japanese Participants

Start date: November 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to understand the relationship of 3 different dosage forms of baricitinib. This study will also explore the effect of food on how the body absorbs baricitinib. This study will last about 5 weeks, not including screening. Screening is required within 28 days prior to the date of first dosing.

NCT ID: NCT02263781 Not yet recruiting - Obesity Clinical Trials

PREPL in Health and Disease

PHD
Start date: October 2014
Phase: N/A
Study type: Interventional

Evaluation of PREPL activity in healthy controls and known or possible PREPL deficient patients

NCT ID: NCT02263547 Terminated - Healthy Volunteers Clinical Trials

Rapid Elimination Procedure of Teriflunomide With Colestipol Hydrochloride

TERCOL
Start date: March 2015
Phase: Phase 1
Study type: Interventional

Primary Objective To determine if colestipol hydrochloride tablets can accelerate the elimination of teriflunomide. Teriflunomide will be administered for 14 days followed by colestipol dosing of 11 days. Total duration of the study is 40 days. Secondary Objectives To collect information on the pattern of side effects with use of colestipol hydrochloride after teriflunomide administration and to determine the best duration of therapy needed for adequate elimination

NCT ID: NCT02257879 Withdrawn - Healthy Volunteers Clinical Trials

DHB Supplement Interaction Study

Start date: October 3, 2014
Phase:
Study type: Observational

Background: - Drinking grapefruit juice changes how long it takes some medicines to be broken down in the body. Researchers have found that a substance in grapefruit juice called DHB contributes to this effect. Some dietary supplements contain DHB and claim to increase the absorption of any and all supplements, medicine or any other drug. But these usually contain a lot more DHB than a glass of grapefruit juice. Researchers want to study the effects of grapefruit juice and supplements with DHB. Objective: - To compare how a certain dietary supplement (sold as DHB-300 ) versus grapefruit juice affects how long it takes a person s body to break down medicines. Eligibility: - Healthy volunteers ages 18 - 60. Design: - Participants will be screened with medical history, physical exam, and blood and urine tests. - Participants will have 3 treatment visits. Participants cannot drive themselves home from the visits. Each visit lasts about 13.5 hours and includes: - Questions about medications and participant s health. - Vital signs taken. - A finger probe to measure oxygen. - Blood and urine sampling throughout the visit. - An IV line inserted into an arm vein. It will stay there throughout the visit. - Study treatments: - Midazolam hydrochloride a syrup given to make people sleepy. - Loperamide a tablet for treating diarrhea. - 1 glass of water, 1 glass of grapefruit juice, or 1 pill of DHB-300. A different one will be given at each treatment visit. - One week before each visit, participants cannot have certain fruits and juices. They must fast the night before each visit. - For the 3 days after each visit, participants will return to the clinic 4 times. Their vital signs will be checked and blood will be drawn.

NCT ID: NCT02256930 Completed - Healthy Volunteers Clinical Trials

Skin Safety Study to Evaluate the Sensitizing Potential in Healthy Volunteers

Start date: September 2014
Phase: Phase 1
Study type: Interventional

This is a single center, randomized, controlled, within subject comparison, multiple dose study to determine the sensitization potential of M518101 on normal skin under occlusive patch condition.