Safety of and Immune Response to a Dengue Virus Vaccine (rDEN3/4delta30[ME]) in Healthy Adults

Dengue Clinical Trial

Official title:

Phase 1 Study of the Safety and Immunogenicity of rDEN3/4delta30(ME), a Live Attenuated Virus Vaccine Candidate for the Prevention of Dengue Serotype 3

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00375726
• Other study ID #: CIR 228
• Secondary ID: WIRB Protocol Nu
• Status: Completed
• Phase: Phase 1
• First received: September 12, 2006
• Last updated: December 13, 2010
• Start date: October 2006
• Est. completion date: September 2008

Study information

• Verified date: December 2010
• 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 rDEN3/4delta30(ME) vaccine is a live attenuated dengue virus vaccine that may be protective against dengue virus serotype 3 (DEN3). The purpose of this study is to evaluate the safety and immunogenicity of the rDEN3/4delta30(ME) vaccine in healthy adults.

This study will last 40 weeks. Participants will be randomly assigned to receive one of three doses of rDEN3/4delta30(ME) or placebo. Participants in Group 1 will receive the middle dose of rDEN3/4delta30(ME) or placebo at study entry. Group 2a will begin enrollment after the immunogenicity review of all participants in Group 1. Participants in Group 2a will receive the highest dose of rDEN4delta30(ME) or placebo at study entry. Group 2b will begin enrollment after the immunogenicity review of all participants in Group 2a. Participants in Group 2b will receive the lowest dose of rDEN4delta30(ME) or placebo.

After vaccination, participants in all groups will be followed closely every other day for the first 16 days of the study. Participants will take their temperature three times a day through Day 16 and record each measurement in a diary. After Day 16, participants will have study visits on Days 21, 28, 42, and 180; a physical exam and blood collection will occur at all visits. Some participants may be asked to join a skin biopsy substudy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 58
• Est. completion date: September 2008
• Est. primary completion date: September 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Good general health

• Available for the duration of the study

• Willing to use acceptable forms of contraception for the duration of the study

Exclusion Criteria:

• Significant neurologic, heart, lung, liver, rheumatologic, autoimmune, or kidney disease

• Behavioral, cognitive, or psychiatric disease that, in the opinion of the investigator, may interfere with the study

• Significant laboratory abnormalities

• Medical, work, or family problems as a result of alcohol or illegal drug use within 12 months prior to study entry

• History of severe allergic reaction or anaphylaxis

• Emergency room visit or hospitalization for severe asthma within 6 months prior to study entry

• HIV-1 infected

• Hepatitis C virus (HCV) infected

• Hepatitis B surface antigen positive

• Immunodeficiency syndrome

• Use of corticosteroids or immunosuppressive medications within 30 days prior to study entry. Participants using topical or nasal corticosteroids are not excluded.

• Live vaccine within 4 weeks prior to study entry

• Killed vaccine within 2 weeks prior to study entry

• Absence of spleen

• Blood products within 6 months prior to study entry

• Previous dengue virus or other flavivirus (e.g., yellow fever virus, St. Louis encephalitis, West Nile virus) infection

• Previously received yellow fever or dengue vaccine

• Plans to travel to an area where dengue infection is common

• Received an investigational agent within 30 days prior to study entry

• Other condition that, in the opinion of the investigator, would interfere with the study

• Pregnancy or breastfeeding

Study Design

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

Related Conditions & MeSH terms

• Dengue

Intervention

Biological:
• rDEN3/4delta30(ME)
Live attenuated rDEN3/4delta30(ME) vaccine (one of three doses)
• Placebo
Placebo for rDEN3/4delta30(ME)

Locations

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

Sponsors (2)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	Johns Hopkins Bloomberg School of Public Health

Country where clinical trial is conducted

United States, 

References & Publications (4)

Blaney JE Jr, Durbin AP, Murphy BR, Whitehead SS. Development of a live attenuated dengue virus vaccine using reverse genetics. Viral Immunol. 2006 Spring;19(1):10-32. Review. — View Citation

Blaney JE Jr, Hanson CT, Firestone CY, Hanley KA, Murphy BR, Whitehead SS. Genetically modified, live attenuated dengue virus type 3 vaccine candidates. Am J Trop Med Hyg. 2004 Dec;71(6):811-21. — View Citation

Blaney JE Jr, Matro JM, Murphy BR, Whitehead SS. Recombinant, live-attenuated tetravalent dengue virus vaccine formulations induce a balanced, broad, and protective neutralizing antibody response against each of the four serotypes in rhesus monkeys. J Virol. 2005 May;79(9):5516-28. — View Citation

Durbin AP, Whitehead SS, McArthur J, Perreault JR, Blaney JE Jr, Thumar B, Murphy BR, Karron RA. rDEN4delta30, a live attenuated dengue virus type 4 vaccine candidate, is safe, immunogenic, and highly infectious in healthy adult volunteers. J Infect Dis. 2005 Mar 1;191(5):710-8. Epub 2005 Jan 27. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety, as defined by frequency of vaccine-related adverse events, as classified by both intensity and severity through active and passive surveillance		Throughout study	Yes
Primary	Immunogenicity, as determined by anti-DEN3 neutralizing antibody measured on Days 0, 21, 28, 42, and 180		Throughout study	No
Secondary	Assess the frequency, quantity, and duration of viremia in each dose cohort studied		Throughout study	No
Secondary	Determine the number of vaccinees infected with rDEN3/4delta30(ME)		Throughout study	No
Secondary	Determine cellular targets of vaccine infection, including peripheral blood mononuclear cells (PBMCs) and skin from participants who are willing to undergo skin biopsy		Throughout study	No
Secondary	Compare the infectivity rates, safety, and immunogenicity between dose groups		At study completion	No
Secondary	Evaluate the immunopathological mechanism of vaccine-associated rash in those volunteers who are willing to undergo skin biopsy		Throughout study	No