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

Dengue Fever Clinical Trial

Official title:

Safety and Immunogenicity of a 2-Dose Regimen of rDEN2/4Δ30 Dengue Vaccine With Boosting at 4 Versus 6 Months

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00920517
• Other study ID #: CIR 250
• Status: Completed
• Phase: Phase 1
• First received: June 11, 2009
• Last updated: December 31, 2012
• Start date: January 2009
• Est. completion date: January 2010

Study information

• Verified date: December 2012
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

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.

Description:

Dengue viruses, which cause dengue fever and dengue shock syndrome, are a major cause of morbidity and mortality in several of the world's tropical and subtropical regions. The rDEN2/4delta30(ME) vaccine is a live attenuated dengue virus vaccine that may be protective against dengue virus serotype 2 (DEN2). The purpose of this study is to evaluate the safety and immunogenicity of the rDEN2/4delta30(ME) vaccine in healthy adults.

This study will last approximately 5 to 7 months with 25 study visits. Participants will be randomly assigned into one of two cohorts. Participants in Cohort 1 will receive an injection of rDEN2/4delta30(ME) or placebo vaccine at Days 0 and 180. Participants in Cohort 2 will receive an injection of rDEN2/4delta30(ME) or placebo vaccine at Days 0 and 120. Participants will be asked to record their temperature in a diary for 16 days after each vaccination. At each study visit a physical examination, symptom history, and blood and urine collection will occur.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: January 2010
• Est. primary completion date: January 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Good general health as determined by means of the screening procedures.

• Available for the duration of the study (32 weeks for cohort 1 and 23 weeks for cohort 2)

• Willing to use effective methods of contraception

Exclusion Criteria:

• Evidence of clinically significant neurologic, cardiac, pulmonary, hepatic, rheumatologic, autoimmune, or renal disease by history, physical examination, and/or laboratory studies

• Behavioral, cognitive, or psychiatric disease that in the opinion of the investigator will affect the ability of the volunteer to understand and cooperate with the requirements of the study protocol

• Neutropenia as defined by an ANC =1500/mm3

• ALT level above the laboratory-defined upper limit of normal

• Serum creatinine level above the laboratory-defined upper limit of normal

• Any other condition that, in the opinion of the investigator, would jeopardize the safety or rights of a volunteer participating in the trial or would render the subject unable to comply with the protocol.

• Medical, occupational, or family problems as a result of alcohol or illicit drug use during the past 12 months

• History of a severe allergic reaction or anaphylaxis

• Severe asthma (emergency room visit or hospitalization within the last 6 months)

• Positive HIV-1 serology by screening and confirmatory assays

• Positive for hepatitis C virus (HCV) by screening and confirmatory assays

• Positive hepatitis B surface antigen (HBsAg) by enzyme-linked immunosorbent assay (ELISA)

• Known immunodeficiency syndrome

• Use of corticosteroids (excluding topical or nasal) or immunosuppressive drugs within 30 days of starting this study

• Receipt of a live vaccine within the 4 weeks or a killed vaccine within the 2 weeks prior to entry into the study

• Has had spleen surgically removed

• Receipt of blood products within the 6 months prior to study entry

• History or serologic evidence of previous dengue virus infection or other flavivirus infection (e.g. yellow fever virus, St. Louis encephalitis, West Nile virus).

• Previous receipt of yellow fever or dengue vaccine (licensed or experimental)

• Persons who have received any investigational agent in the 30 days prior to study entry

• Persons who have definite plans to travel to a dengue endemic area during the study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Dengue
• Dengue Fever

Intervention

Biological:
• rDEN2/4delta30(ME) vaccine
10^3 PFU dose
• Placebo
placebo for rDEN2/4delta30(ME) vaccine

Locations

Country	Name	City	State
United States	Center for Immunization Research	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine the frequency of vaccine related AEs for each dose, graded by severity.		Throughout study	Yes
Primary	Compare the immunogenicity of the two 2-dose regimens of the rDEN2/4?30(ME) candidate vaccine as assessed by neutralizing antibody titers to DEN2		At 4 and 6 weeks after each vaccination	No
Secondary	Assess the frequency, quantity, and duration of viremia after each dose of vaccine.		Throughout study	No
Secondary	Determine the number of vaccinees infected with rDEN2/4?30(ME)		Throughout study	No
Secondary	Comparison of infectivity rates, safety, and immunogenicity between dose 1 and dose 2 withhin cohort and between cohorts		Throughout study	No
Secondary	Evaluation of the phenotype and activation of peripheral blood mononuclear cells at primary infection and upon reinfection with the DEN2/4?30(ME) vaccine.		Throughout study	No