Safety of and Immune Response to a Dengue Virus Vaccine (rDEN3-3'Ddelta30) in Healthy Adults

National Institute of Allergy and Infectious Diseases (NIAID)29 enrolled

Overview

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

Dengue viruses cause dengue fever and the more severe dengue hemorrhagic fever/shock syndrome. More than 2 billion people living in tropical and subtropical regions of the world are at risk of dengue virus infection, which is the leading cause of hospitalization and death in children in several tropical Asian countries. This study will evaluate the safety and immunogenicity of a live attenuated dengue virus vaccine called rDEN3-3'D4delta30. This vaccine is derived from rDEN4delta30, another dengue virus vaccine candidate that has been shown to be safe and immunogenic in Phase I and II trials in healthy adults. There will be two groups in this study. Participants in Group 1 will be randomly assigned to receive rDEN3-3'D4delta30 vaccine or placebo at study entry. The dosing for Group 2 will be determined by a safety review of all participants in Group 1. If less than 90 % of the Group 1 participants seroconvert to DEN3 participants in Group 2 will receive a higher dose of rDEN3-3'D4delta30. If at least 90 % of Group 1 participants seroconvert to DEN3, participants in Group 2 will receive a lower dose of rDEN3-3'D4delta30. All participants will be required to monitor their temperature three times each day for the first 16 days following each vaccination. Study visits will occur 30 minutes following each vaccination and every other day after vaccination until Day 16, followed by four additional visits at selected days through Day 180. Blood collection, vital signs measurement, and a targeted physical exam will occur at each study visit. Some participants will be asked to undergo a skin biopsy or additional blood collection at selected visits.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

DOUBLE

Enrollment

Conditions

Dengue

Interventions

rDEN3-3'D4delta30BIOLOGICAL

Live attenuated 10\^3 dose of rDEN3-3'D4delta30 vaccine.

rDEN3-3'D4delta30BIOLOGICAL

Live attenuated 10\^5 dose of rDEN3-3'D4delta30 vaccine.

rDEN3-3'D4delta30BIOLOGICAL

Live attenuated 10\^1 dose of rDEN3-3'D4delta30 vaccine.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 50 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * General good health * Available for the duration of the study * Willing to use accepted forms of contraception Exclusion Criteria: * Clinically significant neurologic, heart, lung, liver, rheumatologic, autoimmune, or kidney disease by history, physical examination, or laboratory studies including urinalysis * Behavioral, cognitive, or psychiatric disease that, in the opinion of the investigator, may interfere with the study * Certain abnormal laboratory values. More information on this criterion can be found in the protocol. * Medical, work, or family problems as a result of alcohol or illegal drug use within 12 months of study entry * History of severe allergy or anaphylaxis * Severe asthma requiring an emergency room visit or hospitalization within 6 months of study entry * HIV infected * Hepatitis C virus infected * Hepatitis B surface antibody positive * Known immunodeficiency syndrome * Use of corticosteroids or immunosuppressive drugs 30 days prior to study entry. Participants who have used topical or nasal corticosteroids are not excluded. * Receipt of live vaccine within 4 weeks of study entry * Receipt of killed vaccine within 2 weeks of study entry * Absence of spleen * Plan to travel to an area where dengue virus is common * Any investigational product within 30 days of study entry * Other condition that, in the opinion of the investigator, would interfere with the study * Pregnancy or breastfeeding

Locations (2)

Center for Immunization Research, Johns Hopkins School of Public Health

Washington D.C., District of Columbia, United States

Center for Immunization Research, Johns Hopkins University of Public Health

Baltimore, Maryland, United States

Outcomes

Primary Outcomes

Safety and immunogenicity, as assessed by neutralizing antibody titers

Time frame: At 4 weeks and 6 weeks after vaccination

Frequency of vaccine related adverse events as graded by severity

Time frame: Throughout study

Secondary Outcomes

Frequency, quantity, and duration of viremia after a single dose of vaccine

Time frame: Throughout study

Number of vaccines infected with rDEN3-3'D4delta30

Time frame: Throughout study

Infectivity rates, safety, and immunogenicity of a single dose of rDEN3-3'D4delta30 vaccine

Time frame: Throughout study

Durability of antibody response

Time frame: At 26 Weeks after vaccination

Obtain an estimate for the Human Infectious Dose-50% (HID50) idf dose dependent infectivity is observed

Time frame: Throughout study

Data from ClinicalTrials.gov

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