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Healthy Volunteers Clinical Trials

A listing of Healthy Volunteers medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.


Found (15) clinical trials

ICON  Early  Phase  Services  is  conducting  a  research  study  for  healthy  adults  ages 18-65. This study is being  done  to test a  potential treatment for neurodegenerative diseases  (e.g.,  Parkinson's  and Alzheimer's). Vital  signs,  ECGs,  physical  examinations  and  pregnancy,  drug  and  alcohol  screens will be performed.  Blood  and  urine  samples  will ...


Healthy volunteers needed for a vaccine study  Wake Research Associates is enrolling healthy volunteers in a clinical research study of an investigational smallpox vaccine.   Insurance is not needed to participate in this study.

Phase N/A

ICON Early Phase Services is conducting a research study for healthy adults ages 18-55. This study is being done to test the interaction of the study drugs.  This study will help in the development of a potential treatment for pulmonary arterial hypertension (PAH). Vital signs, ECGs, physical examinations and pregnancy, ...


A Study to Evaluate Drug-Drug Interaction of TAK-788 With Itraconazole and Rifampin in Healthy Adult Participants

The drug being tested in this study is called TAK-788. The study will assess the drug-drug interaction of TAK-788 with either a strong cytochrome P-450 (CYP)3A inhibitor, itraconazole (Part 1) or with a strong CYP3A inducer, rifampin (Part 2) in healthy adult participants. The study will enroll approximately 28 healthy ...


Copeptin After an Oral Stimulation With Macimorelin in Healthy Volunteers

Copeptin measurements upon intravenous arginine stimulation discriminate patients with diabetes insipidus versus patients with primary polydipsia with a high diagnostic accuracy. An oral test would be easier to perform, causes less risks and discomfort for the patients and would require less resources in clinical practice. This study investigates stimulation of ...

Phase N/A

Safety and Tolerability of BION-1301 in Healthy Volunteers and Adults With IgA Nephropathy (IgAN)

This is a Phase 1 study of BION-1301, a first-in-class humanized IgG4 anti-a proliferation-inducing ligand (APRIL) monoclonal antibody. The study will be conducted in three parts. Part 1: double-blind, randomized, placebo-controlled, single ascending dose (SAD) in healthy volunteers (HVs). Part 2: double-blind, randomized, placebo-controlled multiple ascending dose (MAD) in HVs. ...


PK Sampling After IV Oxytocin and Effects on Sensory Function in Healthy Volunteers

The primary goal of this protocol is to model change in oxytocin concentrations in plasma after intravenous administration, (oxytocin (Pitocin), 10 IU) the investigators will also acquire tests of sensory function that could be modulated by oxytocin during later time periods when blood samples are widely separated by time. There ...


A Study to Demonstrate the Equivalent Pharmacokinetic Properties of a Single Intravenous Dose of HD201 and EU-Herceptin and US-Herceptin in Healthy Male Subjects

This is a double-blind, randomised, parallel group study, where a total of 105 healthy adult male volunteers, 18 and 55 years of age, non-smoker, will be dosed; 35 subjects per treatment group, randomly assigned to one of the 3 treatment arms.


A Study in Healthy Volunteers and Patients With Mild Asthma to Investigate the Safety Anti-inflammatory Effect of Inhaled AZD0449.

Part 1a of the study with six inhaled dose levels of AZD0449 nebulized suspension are planned to be investigated in 6 cohorts. Depending on emerging safety and PK data, up to 3 additional inhaled dose levels (cohorts), within the pre-specified dose range may be added at the discretion of the ...


Safety Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers

This is a randomized and double-blinded within study group, placebo-controlled trial to evaluate the safety, tolerability and immunological profile of INO-4500 administered by intradermal (ID) injection followed by electroporation using the CELLECTRA 2000 device in healthy adult volunteers.