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Virus Diseases clinical trials

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NCT ID: NCT00727597 Completed - Clinical trials for Human Immunodeficiency Virus Infections

A Study in Underrepresented Patient Population or Regimen Tolerability: SUPPoRT

SUPPoRT
Start date: July 2008
Phase: Phase 3
Study type: Interventional

The hope of this study is to gather data and information about the tolerability and effectiveness of Lexiva versus Sustiva in patients who have have been generally underrepresented in clinical trials.

NCT ID: NCT00722774 Completed - Influenza Clinical Trials

Safety and Immune Response to Recombinant Live-Attenuated Influenza H2N2 Virus Vaccine

Start date: n/a
Phase: Phase 1
Study type: Interventional

In the 20th century, influenza pandemics occurred in 1918, 1957, and 1968, and were associated with significant morbidity and mortality. It is estimated that, in the United States alone, the next influenza pandemic could cause approximately 200,000 deaths and 750,000 hospitalizations. Thus, the development of a vaccine against potential influenza strains has become a priority. The purpose of this study is to determine the safety and immune response to an H2N2 influenza vaccine candidate.

NCT ID: NCT00717834 Completed - Clinical trials for Ross River Virus Disease (RRVD)

Safety and Immunogenicity Study of a Ross River Virus (RRV) Vaccine

Start date: June 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of this study is to assess the safety and tolerability of the Ross River Virus (RRV) Vaccine in a healthy young adult population. Other objectives of this study are to assess the immunogenicity of the RRV Vaccine in a healthy young adult population and to identify the optimal dose level of the RRV Vaccine in a healthy young adult population.

NCT ID: NCT00711009 Completed - Clinical trials for Human Immunodeficiency Virus Infection

Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxil Fumarate (FTC/TDF) With a Nucleoside Sparing Regimen Consisting of Lopinavir/Ritonavir + Raltegravir (RAL)

PROGRESS
Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the safety, tolerability, and antiviral activity of the lopinavir/ritonavir tablet when administered in combination with reverse transcriptase inhibitors to lopinavir/ritonavir tablets when administered in combination with a human immunodeficiency virus type 1 ( HIV-1) integrase inhibitor in antiretroviral naive HIV-1 infected subjects.

NCT ID: NCT00707642 Completed - Clinical trials for West Nile Virus Disease

Safety Study of HBV-002 West Nile Vaccine in Healthy Adults

Start date: May 2008
Phase: Phase 1
Study type: Interventional

The purpose of this Phase 1 trial is to evaluate the clinical safety of HBV-002 vaccine in healthy adults.

NCT ID: NCT00701922 Completed - Clinical trials for Lung Transplantation

Surveillance Study of Viral Infections Following Lung Transplantation

Start date: October 2005
Phase: N/A
Study type: Observational

The present study was conducted to study the impact community acquired respiratory virus (CARV) infections in an outpatient setting on graft function of lung transplant recipients. The study was aimed to identify risk factors for CARV infections. The study was further intended to investigate an association of Epstein-Barr virus (EBV), cytomegalovirus (CMV) and human adenovirus (HAdV) with the development of BOS and to identify risk factors for virus detection in blood.

NCT ID: NCT00668369 Completed - Clinical trials for Liver Transplantation

Effect of Immunosuppression Drug Weaning on Hepatitis C Virus (HCV)-Induced Liver Damage After Liver Transplantation

Start date: April 2008
Phase: Phase 2
Study type: Interventional

Viral infections can profoundly influence alloimmune responses and hamper allograft tolerance induction. Persistent hepatitis C virus (HCV) infection occurs in 50% of liver and 20% of kidney transplant recipients, but the impact of HCV on the acquisition of allograft tolerance has not been elucidated. Liver transplantation constitutes a unique clinical model to address this question, given that up to 20% of liver recipients can completely discontinue immunosuppressive drugs and attain operational tolerance. The goal of our study is to determine the influence of HCV-driven immune responses on the acquisition of operational tolerance in liver transplant recipients following drug weaning, and to assess whether immunosuppression withdrawal ameliorates HCV-induced liver damage. This is a prospective trial in which immunosuppressive drug weaning will be offered to HCV-positive liver recipients (selected on the basis of a high likelihood of tolerance) as a strategy to improve HCV-mediated liver disease.

NCT ID: NCT00667303 Completed - Clinical trials for Respiratory Virus Infections

Prospective Surveillance For Respiratory Virus Infections In Children Undergoing Hematopoietic Stem Cell Transplantation

Start date: December 2007
Phase: N/A
Study type: Observational

The Study aims to prospectively survey the incidence of respiratory virus infections using molecular methodologies, in children undergoing hematopoietic stem cell transplantation

NCT ID: NCT00658086 Completed - Clinical trials for Respiratory Syncytial Virus Infections

Phase 2 Study of ALN-RSV01 in Lung Transplant Patients Infected With Respiratory Syncytial Virus (RSV)

Start date: April 2008
Phase: Phase 2
Study type: Interventional

To evaluate the safety,tolerability and antiviral activitity of ALN-RSV01 in RSV infected lung transplant patients

NCT ID: NCT00641017 Completed - Virus Diseases Clinical Trials

Safety of and Immune Response to Recombinant Live-Attenuated Parainfluenza Type 1 Virus Vaccine

Start date: March 2008
Phase: Phase 1
Study type: Interventional

Human Parainfluenza Virus Type 1 (HPIV1) is a leading cause of viral respiratory infections in children, the elderly, and those with compromised immune systems. HPIV1 is also the leading cause of viral croup in children under 6 years old. The purpose of this study is to determine the safety of and immune response to a HPIV1 vaccine, rHPIVI1 84/del170/942A, in 2 groups of adults and then in children who have been previously exposed to HPIV1. Once the safety of this vaccine has been established in these groups, an additional 2 groups of infants and children who have not been previously exposed to HPIV1 will be vaccinated. Naïve infants and children are the most vulnerable to naturally circulating HPIV1 and are the target population of this vaccine.