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Healthy Volunteers clinical trials

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NCT ID: NCT02122692 Completed - Healthy Volunteers Clinical Trials

Effect of Multiple Doses of Itraconazole on the Multiple Dose Pharmacokinetics of Lu AE58054 in Healthy Subjects

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

To examine the effect of the strong CYP3A4/5 inhibitor itraconazole (200 mg QD) on the multipledose exposure of Lu AE58054 (30 mg QD) in healthy subjects (CYP2D6 extensive metabolisers).

NCT ID: NCT02121834 Completed - Healthy Volunteers Clinical Trials

A Study of LY3050258 in Healthy Participants

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

This is a multiple dose study of LY3050258 in healthy men and postmenopausal women. This study will evaluate the safety and how well the body tolerates LY3050258. It will last approximately 14 weeks with a 2 week follow-up appointment after the last treatment with study drug.

NCT ID: NCT02121080 Completed - Healthy Volunteers Clinical Trials

Study of the Safety and Tolerability of REGN2222(SAR438584) in Healthy Adult Volunteers

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

This is a phase 1, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, pharmacokinetic (PK) profile, and immunogenicity of REGN2222 ascending in cohorts of healthy adult volunteers.

NCT ID: NCT02119637 Completed - Healthy Volunteer Clinical Trials

Effects of Transcranial Magnetic Stimulation (TMS) on Somatosensory Perception

Start date: April 17, 2014
Phase:
Study type: Observational

Background: - Different parts of the brain are involved in feeling touch. Researchers want to study whether repetitive magnetic stimulation (rTMS) to the sensory cortex affects how sensation feels. rTMS is a repeated magnetic pulse that interferes with brain activity. It affects a small part of the brain beneath the scalp. Researchers want to find out the role of sensory cortex in sensing different types of touch. Objectives: - To find out the role of sensory cortex, a brain area, in sensing different types of touch. Eligibility: - Healthy adults ages 18 45. Design: - Participants will be pre-screened with a telephone interview. Then they will be screened with physical and psychological exams and a urine test. - In Session 1, participants will have an MRI brain scan and fill out questionnaires. - For MRI, a magnetic field and radio waves take pictures of the brain. Participants will lie on a table that slides in and out of a metal cylinder. A coil will be placed over their head. They will perform a task during the scan. The scanner makes loud knocking noises. Participants will get earplugs. They will be in the scanner for up to 60 minutes. - In Sessions 2 and 3, participants will take urine tests. Their perception of touch will be measured. Then rTMS will be used to stimulate their sensory cortex and scalp for about 20 minutes. Their perception of touch will be measured again. - For rTMS, a wire coil is held on the scalp. A brief electrical current passes through the coil and creates a magnetic pulse that affects activity in the brain.

NCT ID: NCT02119221 Completed - Healthy Volunteers Clinical Trials

Copanlisib Mass Balance Study

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

The study aims to provide understanding of the relative relevance of the different excretion pathways of Copanlisib in humans, as well as to characterize its metabolite profile.

NCT ID: NCT02118909 Completed - Healthy Volunteers Clinical Trials

Evaluate the Effects of Itraconazole and Ciprofloxacin on Single-Dose PK of Pracinostat in Healthy Nonsmoking Subjects

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

This study is designed as a 2-part, open-label study to assess the effect of pracinostat with itraconazole (part 1) and pracinostat with ciprofloxacin (part 2) on the bioavailability of pracinostat. Secondarily to evaluate the safety and tolerability of pracinostat administered with itraconazole or ciprofloxacin.

NCT ID: NCT02117752 Completed - Healthy Volunteers Clinical Trials

Dermal Tolerability of Dapsone Gel in Healthy Volunteers

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

This study will determine the cumulative irritation potential and sensitization potential of dapsone gel and vehicle after repeat applications on the skin of healthy volunteers.

NCT ID: NCT02117739 Completed - Healthy Volunteers Clinical Trials

Photoallergy Potential of Dapsone Gel in Healthy Volunteers

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

This study will evaluate the potential of dapsone gel and its vehicle to cause a photoallergic reaction after repeated application and irradiation to the skin of healthy volunteers under controlled conditions.

NCT ID: NCT02111083 Completed - Healthy Volunteers Clinical Trials

A Study of 2 Different Formulations of Insulin Lispro in Healthy Participants

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

The study involves 4 injections of insulin lispro and its purpose is to: - Determine if 2 formulations of insulin lispro are treated by the body in a similar way. - Compare how the 2 formulations of insulin lispro affect blood sugar level. - Determine the safety of each insulin lispro formulations and any side effects that might be associated with them when given to healthy participants. The study is expected to last up to approximately 9 weeks for each participant.

NCT ID: NCT02110875 Completed - Healthy Volunteers Clinical Trials

Strength and Balance in Gender- and Age-Matched Controls

VITDC
Start date: June 2013
Phase: N/A
Study type: Observational

The purpose of this study is to learn more about balance and strength in an elderly population (60 and older). Data will be compared between controls and the age/gender- matched PD participants in study "The Effects of vitamin D on Balance in Parkinson's disease" (OHSU IRB # 6482). Specifically a t-test will be used to compare total work and total power on leg extension and flexion, composite SOT score conditions 1-3 and 4-6, response strength and latency on MCT, and turn duration from the iMOBILITY between the two groups.