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Dengue clinical trials

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NCT ID: NCT01084291 Completed - Dengue Virus Clinical Trials

Evaluation of the Safety and Immune Response to an Investigational Dengue Type 1 Vaccine

Start date: April 2010
Phase: Phase 1
Study type: Interventional

Dengue viruses can cause dengue fever and other serious health conditions, primarily affecting people living in tropical regions of the world. There are four types of dengue virus, and infection with one does not offer protection against the others. This study will test whether a vaccine developed to prevent infection with dengue virus type 1 (DEN1) causes a response in people's immune system and is safe.

NCT ID: NCT01073306 Completed - Dengue Virus Clinical Trials

Safety and Immune Response to an Investigational Dengue Type 2 Vaccine

Start date: February 2010
Phase: Phase 1
Study type: Interventional

Dengue viruses can cause dengue fever and other serious health conditions, primarily affecting people living in tropical regions of the world. This study will test whether a vaccine developed to prevent infection with dengue virus type 2 causes a response in people's immune system and is safe.

NCT ID: NCT01072786 Completed - Dengue Clinical Trials

Evaluation of the Safety and Immune Response of Five Admixtures of a Tetravalent Dengue Virus Vaccine

Start date: July 2010
Phase: Phase 1
Study type: Interventional

Dengue viruses can cause dengue fever and other serious health conditions, primarily affecting people living in tropical regions of the world. This study will evaluate the safety and immune responses of five formulations of a tetravalent dengue virus vaccine in healthy adults.

NCT ID: NCT01064141 Completed - Dengue Fever Clinical Trials

A Study of Dengue Vaccine in Healthy Toddlers Aged 12 to 15 Months in the Philippines

Start date: January 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the potential for co-administration of the first dose of CYD Dengue vaccine with childhood vaccination. Primary Objectives: - To describe the safety of CYD Dengue vaccine after each dose; first dose given alone or coadministered with childhood vaccines. Secondary Objectives: - To describe the immunogenicity of CYD Dengue vaccine after each dose; first dose given alone or co-administered with childhood vaccines.

NCT ID: NCT01030211 Completed - Dengue Fever Clinical Trials

Adult Dengue Platelet Study

ADEPT
Start date: January 2010
Phase: N/A
Study type: Interventional

Retrospective data in children with dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS), and in adults with dengue fever (DF), suggested a lack of benefit from prophylactic platelet transfusion for severe thrombocytopenia in dengue patients without bleeding. However, in Taiwan and Singapore, platelet transfusion was given to 13-50% of hospitalised dengue patients. This is a prospective randomised study to examine the safety and efficacy of prophylactic platelet transfusion in adults with dengue and severe thrombocytopenia without bleeding. The hypotheses are: 1. Prophylactic platelet transfusion is safe in hospitalised dengue patients with severe thrombocytopenia. 2. Prophylactic platelet transfusion is effective in preventing bleeding in hospitalised dengue patients with severe thrombocytopenia.

NCT ID: NCT00993447 Completed - Dengue Clinical Trials

Immunogenicity and Safety of Sanofi Pasteur's CYD Dengue Vaccine in Healthy Children and Adolescents in Latin America

Start date: October 2009
Phase: Phase 2
Study type: Interventional

Primary objectives: - To describe the immune response to each dengue serotype before and after each vaccination with sanofi pasteur's CYD dengue vaccine. - To evaluate the safety of each vaccination with sanofi pasteur's CYD dengue vaccine.

NCT ID: NCT00946218 Completed - Dengue Fever Clinical Trials

Diagnosis and Characterization of Dengue Fever in Children

Start date: July 2009
Phase: N/A
Study type: Observational

Dengue virus is an arbovirus transmitted by mosquitoes which causes significant morbidity and mortality among children in tropical regions, especially in resource limited countries. The objective of this protocol is to compare the sensitivity and specificity of clinical gestalt and two rapid antigen tests for dengue virus and to compare the gene expression of leukocytes in distinct dengue fever disease phenotypes module-based RNA microarray technology.

NCT ID: NCT00936429 Completed - Dengue Fever Clinical Trials

Study of HBV-001 D1 in Healthy Adults

Start date: July 2009
Phase: Phase 1
Study type: Interventional

This is a single-center, double-blind, randomized, Phase 1 study to assess the safety and tolerability of HBV-001 D1 in healthy adult subjects.

NCT ID: NCT00920517 Completed - Dengue Fever Clinical Trials

Safety and Immune Response to Two Doses of rDEN2/4delta30 Dengue Vaccine

Start date: January 2009
Phase: Phase 1
Study type: Interventional

Dengue fever, caused by dengue viruses, is a major health problem in the tropical and subtropical regions of the world. The purpose of this study is to test the safety of and immune response to a new dengue virus vaccine in healthy adults.

NCT ID: NCT00919178 Completed - Clinical trials for Dengue Hemorrhagic Fever

Safety of and Immune Response to DEN4 Vaccine Component Candidate for Dengue Virus

Start date: July 2009
Phase: Phase 1
Study type: Interventional

Infection with dengue viruses is one of the leading causes of hospitalization and death in children in several tropical Asian counties. The World Health Organization (WHO) estimates that these viruses are responsible for more than 50 million cases of dengue fever (DF) and approximately 0.5 million cases of the more severe disease, dengue hemorrhagic fever/ shock syndrome (DHF/DSS) annually. Because dengue viruses are endemic in most tropical and subtropical regions, keeping more than 2 billion persons at risk for acquiring dengue, the WHO has made development of a dengue vaccine a top priority. The purpose of this study is to evaluate the safety and effectiveness of a candidate DEN4 vaccine aimed at preventing infection with dengue virus serotype 4.