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Healthy Volunteers clinical trials

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NCT ID: NCT01650597 Completed - Healthy Volunteers Clinical Trials

A Single Ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of JNJ-42165279 in Healthy Male Participants

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

The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of single ascending doses as well as repeated doses of JNJ-42165279 in healthy male participants.

NCT ID: NCT01648790 Completed - Healthy Volunteers Clinical Trials

A Study of Prasugrel in Healthy Participants

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

The purpose of this study is to evaluate the amount of drug available in the body when given to healthy participants as two different formulations with or without a meal. In addition, this study will evaluate how much of the drug gets into the blood stream and how long the body takes to get rid of it. Information about any side effects that may occur will also be collected. Each participant will receive a total of five different treatments. Each treatment is given by mouth, once a day. The treatment period lasts for five consecutive days.

NCT ID: NCT01648283 Completed - Healthy Volunteers Clinical Trials

CYP2B6 Polymorphisms in Methadone Disposition

Start date: November 2012
Phase: N/A
Study type: Interventional

This research study will determine if genetic variation in CYP2B6 affects how the body metabolizes methadone.

NCT ID: NCT01647815 Completed - Healthy Volunteers Clinical Trials

Ultrasound Comparison of the Surface of the Subclavian and the Axillary Vein Versus the Surface of the Subclavian Vein

AnatoAbord
Start date: August 2012
Phase: N/A
Study type: Interventional

The main objective of this study is the demonstration of an increase of over 50% of the surface visible on ultrasound (mm2) of the axillary vein and subclavian vein in arm abduction (90 °) and external rotation (90 °) with respect to the surface of the subclavian vein along the arm body.

NCT ID: NCT01645085 Completed - Healthy Volunteers Clinical Trials

A Study to Assess the Bioequivalence of R406 in Healthy Volunteers When Given 100mg and 150 mg of Fostamatinib

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

A study in Healthy Volunteers to Compare the Amount of R406 in Blood When Given Different Formulations of Fostamatinib.

NCT ID: NCT01644071 Completed - Healthy Volunteers Clinical Trials

Serotonergic System and Violent Video Games

Serogen
Start date: February 2012
Phase: N/A
Study type: Interventional

Aggressive behavior (AB) is a major burden to society with severe socio-economic consequences. Genetic studies suggest a high heritability of AB; in particular, the low expressing allele of the MAOA gene (MAOA-L) has been associated with increased AB. Recent neural aggression models have suggested a dysfunctional emotion regulation circuit including amygdala, orbitofrontal, and anterior cingulate cortex. Dysregulated serotonergic (5-HT) projections from the anterior cingulate cortex to the amygdala have been suggested to promote aggressive behavior. This finding is well in line with the observation that the MAOA-L allele leads to a reduced expression of monoamine oxidase A and thus to an overflow of 5-HT in serotonergic cortico-amygdalar projections. However, due to methodological and ethical constraints, the neural substrates of AB are difficult to assess. A possible solution is the use of virtual violence which permits AB against virtual characters without direct consequences for any real person and can be easily applied in functional imaging experiments. There is evidence that virtual and real aggression share common neural substrates. AB in violent video games inhibits rostral anterior cingulate cortex (ACC) and amygdala in line with the suggested neurophysiological circuits underlying real-life AB.

NCT ID: NCT01638104 Completed - Healthy Volunteers Clinical Trials

ANX-042 Healthy Volunteer Dose Escalation Study

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

The purpose of this study was to investigate the safety and tolerability of ANX-042 when administered by continuous intravenous (IV) infusion in healthy volunteers.

NCT ID: NCT01636531 Completed - Healthy Volunteer Clinical Trials

A Study of A High Concentration Liquid Formulation Versus A Lyophilized Formulation of Gantenerumab in Healthy Volunteers

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

This multi-center, randomized, open-label, single-dose, parallel group study will assess the relative bioavailability, tolerability and dose-exposure relationship of a high concentration liquid formulation (HCLF) versus a lyophilized formulation (LyoF) of gantenerumab (RO4909832) in healthy volunteers. Subjects will be randomized to receive single subcutaneous doses of either HCLF or LyoF. Anticipated time for treatment period and follow-up will be 13 weeks.

NCT ID: NCT01636492 Completed - Healthy Volunteer Clinical Trials

A Study of Bitopertin (RO4917838) in Healthy Male Volunteers

Start date: November 2005
Phase: Phase 1
Study type: Interventional

This randomized, double-blind, placebo-controlled, dose-escalating study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of bitopertin in healthy male volunteers. Subjects will be randomized in cohorts to receive single oral doses of either bitopertin or placebo.

NCT ID: NCT01636440 Completed - Healthy Volunteers Clinical Trials

Reliability of Measuring Conditioned Pain Modulation With the Nociceptive Withdrawal Reflex

Start date: June 2012
Phase: N/A
Study type: Interventional

Conditioned pain modulation is the ability of the spine to describe changes in pain perception, if two different painful stimulations take place. The reliability of the conditioned pain modulation has not been studied, the instruments used to measure the conditioned pain modulation are sparse and have proven difficult to use in a well reproductible way. This study is using an existing pain test, relying on the reflex in a muscle after a painful electrical stimulation. We will test 34 healthy volunteers in order to test the reliability of the conditioned pain modulation with the nociceptive withdrawal reflex combined to a ice water test.