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Healthy Volunteers clinical trials

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NCT ID: NCT02876601 Completed - Healthy Volunteers Clinical Trials

Defibrotide in the Human Endotoxemia Model --‐ an Exploratory Trial Investigating the Effects and the Mechanisms of Defibrotide

LPS_DF
Start date: April 18, 2017
Phase: Phase 4
Study type: Interventional

Defibrotide is an anti-inflammatory and anti-coagulatory agent approved for treatment of veno-occlusive disease. Although it has been in clinical use for almost 30 years, the exact mechanism of action has never been fully elucidated. Thus, the effects of defibrotide will be investigated in the human endotoxemia model in order to gather further information on its actions.

NCT ID: NCT02875028 Completed - Healthy Volunteers Clinical Trials

Vorapaxar in the Human Endotoxemia Model

Start date: June 2016
Phase: Phase 4
Study type: Interventional

Vorapaxar is a recently approved protease activated receptor - 1 (PAR-1) inhibitor. Platelet inhibition may also exert positive results on coagulation activation and may beneficially influence the inflammatory response. Since vorapaxar is the first available substance of a new class of platelet inhibitors its effects on the human coagulation system and the inflammatory response will be assessed in the well-established human endotoxemia model.

NCT ID: NCT02873767 Completed - Healthy Volunteers Clinical Trials

A First-In-Human Study With a Single Dose UCB4019 in Healthy Volunteers

Start date: August 2016
Phase: Phase 1
Study type: Interventional

This study is designed to evaluate the safety and tolerability of single ascending doses of UCB4019 administered by subcutaneous injection in healthy subjects.

NCT ID: NCT02872688 Completed - Healthy Volunteers Clinical Trials

Influence of GanedenBC30 (Bacillus Coagulans GBI-30, 6086) on the Gut Microbiome in Healthy Adults

Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of a GanedenBC30, a probiotic bacteria (Bacillus coagulans strain GBI-30, 6086), on the gut microbiome in healthy adults. Subjects will complete a 2-week run-in period prior to receiving GanedenBC30. The study is open-label and subjects will act as their own controls as the microbiome is unique to individuals. During the run-in period, subjects will collect two stool samples and complete daily bowel habit diaries in order to understand usual habits and profile the microbiome for each subject. 30 subjects will take part in this research study conducted at Nutrasource Diagnostics Inc. Subjects will take GanedenBC30 for four weeks. Stool samples will be collected at the end of the study and daily bowel habit diaries maintained for the duration of the study.

NCT ID: NCT02871648 Completed - Healthy Volunteers Clinical Trials

The Role of Minerelocorticoid Receptor on Modulating Aldosterone Production

Start date: January 2016
Phase: Phase 1
Study type: Interventional

The purpose of this research protocol is to determine if the same effects are observed in vivo in humans using a similar approach. Demonstrating that mineralocorticoid acts on zona glomerulosa cells to regulate aldosterone production in a short feedback loop would provide important insight into hormone regulation, and explain variability in pathophysiologic states such as hypertension and cardiovascular diseases.

NCT ID: NCT02870400 Completed - Healthy Volunteers Clinical Trials

A Study to Examine the Safety and Tolerability of Single Ascending Doses of REGN2477

Start date: July 2016
Phase: Phase 1
Study type: Interventional

The primary objective of the study is to assess the safety and tolerability of single ascending doses of REGN2477 in healthy women not of childbearing potential.

NCT ID: NCT02869893 Completed - Healthy Volunteers Clinical Trials

MRCP: A Reliable, Non Invasive Method for Staging Chronic Pancreatitis in Pediatrics

Start date: August 10, 2016
Phase: N/A
Study type: Interventional

The goal of this research study is to learn more about the pancreas. The investigators want to use Magnetic Resonance Cholangiopancreatography (MRCP) to learn more about the size of a normal pancreas. MRCP is a special kind of MRI exam that produces detailed images of the pancreas. The investigators also want to figure out how much fluid the pancreas releases in response to secretin. Secretin is a chemical in the body that causes the pancreas to release fluid that helps with digestion. Secretin is used during the MRCP (MR-PFT) to help identify dysfunction of the pancreas. MR elastography (MRE) will be used to measure how hard the pancreas is. MRE is a special kind of MRI that uses vibrations to image tissue.

NCT ID: NCT02867098 Completed - Healthy Volunteers Clinical Trials

XmAb5871 Bioavailability Study

Start date: July 2016
Phase: Phase 1
Study type: Interventional

An open label comparison of concentration of the study medication administered intravenously (IV) versus subcutaneously (SC) in healthy volunteers.

NCT ID: NCT02858973 Completed - Healthy Volunteers Clinical Trials

A Dose-Escalation Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of Q203 in Normal Healthy Male and Female Volunteers

Start date: August 2016
Phase: Phase 1
Study type: Interventional

This is randomized, double-blind, placebo-controlled, multiple ascending dose study of Q203 in healthy volunteers conducted at one study center in the United States

NCT ID: NCT02856633 Completed - Hypertension Clinical Trials

Preliminary Testing of the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station

Start date: July 2016
Phase: N/A
Study type: Observational

The study objective is to satisfy the testing requirements for the Qualcomm Tricorder XPRIZE Competition. This requires an oversight model using the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station to continuously monitor the patient's five core vital signs and to detect the health conditions required by the competition.