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Healthy Male Volunteers clinical trials

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NCT ID: NCT01606462 Completed - Clinical trials for Healthy Male Volunteers

Oxytocin and Social Cognition

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

The purpose of this study is to determine whether oxytocin influences memory of social stimuli and reaction to social stimuli. Furthermore the investigators explore the effect of oxytocin receptor (OXTR) polymorphism in terms of behavioral and neural responses to social stimuli.

NCT ID: NCT01577355 Completed - Clinical trials for Healthy Male Volunteers

A Study of LY2784544 in Healthy Male Subjects

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

This is a single dose study of radiolabelled LY2784544 in healthy male subjects to study the absorption, distribution, metabolism and excretion of LY2784544. This study is for research purposes only and is not intended to treat any medical condition.

NCT ID: NCT01549743 Completed - Clinical trials for Healthy Male Volunteers

The Pharmacokinetic Interaction Between Celecoxib and Rebamipide

Start date: May 9, 2012
Phase: Phase 1
Study type: Interventional

This clinical trial aims to assess the pharmacokinetic interaction between celecoxib and rebamipide in healthy male subjects.

NCT ID: NCT01426906 Completed - Clinical trials for Healthy Male Volunteers

Pharmacokinetic Drug Interaction Study in Healthy Male Subjects

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

A Randomized, Open Label, Drug-Drug interaction study to investigate effect of ketoconazole or rifampicin on the Pharmacokinetic characteristics and safety of LC15-0444 in Healthy Male Volunteers.

NCT ID: NCT01382017 Completed - Clinical trials for Healthy Male Volunteers

Effects of Lacosamide on Human Motor Cortex Excitability: a Transcranial Magnetic Stimulation Study

Start date: June 2011
Phase: N/A
Study type: Interventional

This study has been designed to explore dose-depended effects of lacosamide (LCM) on motor cortex excitability with TMS in a randomized, double-blind, placebo-controlled crossover trial in young healthy human subjects, and to compare the pattern of excitability changes induced by LCM with those of carbamazepine (CBZ). LCM selectively enhances slow inactivation of voltage-gated sodium channel, and, in contrast to CBZ, does not affect steady-state fast inactivation (Errington et al., 2006). The enhancement of slow inactivation of sodium channels by LCM is a novel manner to modulate sodium channels and leads to normalization of activation thresholds and a reduced pathophysiological hyper-responsiveness, thereby effectively controlling neuronal hyperexcitability without affecting physiological activity (Beyreuther et al., 2007). Therefore, it is thought that LCM, compared to CBZ, will be better tolerated in clinical settings while being as or even more effective in controlling seizure activity. On the basis of the results from nonhuman studies, it is hypothesized that the TMS profile of LCM will be distinguishable from that of CBZ. CBZ, like other 'classical' sodium channel blockers such as phenytoin, predominantly demonstrated elevated TMS motor thresholds indicating reduced neuronal membrane excitability, without developing significant changes of synaptic intracortical inhibition and facilitation (Ziemann et al., 1996; Chen et al., 1997; Lee et al., 2005). Because of its novel mode of action it can only be speculated which TMS parameters LCM might affect. For example, more than exclusively affecting neuronal membrane excitability, LCM could possibly also affect inhibitory mechanisms such as short- and long-latency intracortical inhibition (Valls-Sole et al., 1992; Kujirai et al., 1993). This would in line with other well-tolerated modern antiepileptic drugs (Ziemann et al., 1996; Reis et al., 2002; Lang et al., 2006).

NCT ID: NCT01367483 Completed - Clinical trials for Healthy Male Volunteers

Study of the Pharmacokinetics of Intravenous Administered 14C-MNTX

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

This is an open-label, radiotracer study, to be conducted in healthy, normal, male volunteers. It will entail intravenous administration of a single dose of 14C-MNTX, collection of excretions, and periodic drawing of blood samples. Exhaled 14CO2 will also be sampled as a measure of the extent of possible metabolic MNTX demethylation.

NCT ID: NCT01356043 Completed - Clinical trials for Healthy Male Volunteers

CKD-828 Drug Interaction Study (S-amlodipine)

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

The purpose of this study is to evaluate the Pharmacokinetic drug interaction and safety of S-amlodipine between free combination of S-amlodipine and Telmisartan and S-amlodipine monotherapy.

NCT ID: NCT01356017 Completed - Clinical trials for Healthy Male Volunteers

CKD-828 Drug Interaction Study (Telmisartan)

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

The purpose of this study is to evaluate the Pharmacokinetic drug interaction and safety of Telmisartan between free combination of Telmisartan and S-amlodipine and Telmisartan monotherapy.

NCT ID: NCT01342055 Completed - Clinical trials for Healthy Male Volunteers

Pharmacokinetics and Safety Study of Apetrol ES in Healthy Male Volunteers

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

A Randomized, Open Label, Single dose, Cross-over, Phase I Trial to Investigate Safety and Pharmacokinetics of Apetrol ES and Megace® under Fed Conditions in Healthy Male Volunteers.

NCT ID: NCT01290900 Completed - Clinical trials for Healthy Male Volunteers

A Single-centre, Randomised, Double-blind, Placebo-controlled, Four Way Crossover Phase I Study to Investigate the Effect on QT/QTc Interval of Ceftazidime NXL104 or Ceftaroline Fosamil NXL104, Compared With Placebo, Using Moxifloxacin (Avelox®) as a Positive Control, in Healthy Male Volunteers

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

This is a single dose study in healthy male volunteers to investigate the effect of high doses of ceftazidime NXL104 (CAZ104) or ceftaroline fosamil NXL104 (CXL104) on the QT interval