A Two-dose Primary Vaccination Study of a Tetravalent Dengue Virus Purified Inactivated Vaccine vs. Placebo in Healthy Adults (in Puerto Rico)

Dengue Fever Clinical Trial

— DPIV-002  

Official title:

A Phase I, Randomized, Placebo-Controlled, Observer-blind, Two-dose (0-28 Day Schedule) Primary Vaccination Study of WRAIR Tetravalent Dengue Virus Purified Inactivated Vaccine (TDENV-PIV) in Healthy Adults in Puerto Rico

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01702857
• Other study ID #: S-12-12
• Secondary ID: 116614WRAIR 1945
• Status: Completed
• Phase: Phase 1
• First received: October 4, 2012
• Last updated: May 22, 2017
• Start date: November 2012
• Est. completion date: March 23, 2017

Study information

• Verified date: May 2017
• Source: U.S. Army Medical Research and Materiel Command
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a first time in humans (FTiH) study designed to assess the experimental TDENV-PIV vaccine in a predominantly dengue-primed adult population. The study is designed to afford a first time in humans (FTiH) safety and immunogenicity assessment of three TDENV-PIV vaccine candidates, each formulated with a different adjuvant: either aluminum hydroxide, AS01E or AS03B (adjuvants used in GSK Biologicals' hepatitis B candidate vaccine, malaria candidate vaccine and pandemic flu vaccine, respectively). Each vaccine candidate will contain 1 µg of purified virus antigen per each of the four DENV types. Additionally, the study will evaluate an alum adjuvanted TDENV-PIV vaccine candidate containing 4 µg of purified virus antigen per each of the four DENV types. The control group will receive a saline placebo. All experimental vaccinations will be administered according to a 2-dose schedule, 28 days apart. There is a parallel FTiH study that is conducted in the United States in a dengue-naive population using the same investigational vaccines.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: March 23, 2017
• Est. primary completion date: January 20, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 39 Years

Eligibility

Inclusion Criteria:

• Subjects who the investigator believes can and will comply with the requirements of the protocol (e.g., completion of the diary cards, return for follow-up visits, etc.)

• A male or female between 20 and 39 years of age (inclusive) at the time of consent

• Written informed consent obtained from the subject

• Healthy subjects as established by medical history and clinical examination before entering into the study

• Subject has lived in the Caribbean for more than 10 years

• Female subjects of non-childbearing potential (non-childbearing potential is defined as having either a current tubal ligation at least three months prior to enrollment, hysterectomy, ovariectomy, or is post-menopause).

• Female subjects of childbearing potential may be enrolled in the study, if the subject has:

• practiced adequate contraception for 30 days prior to vaccination, and

• a negative urine pregnancy test on the day of vaccination, and

• agreed to continue adequate contraception until two months after completion of the vaccination series

Exclusion Criteria:

• Use of any investigational or non-registered product (drug or vaccine) other than the study vaccines/placebo during the period starting 30 days preceding the first dose of study vaccine/placebo and/or planned use during the study period

• Chronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting 180 days prior to the first vaccine/placebo dose (for corticosteroids, this will mean prednisone = 20 mg/day or equivalent; inhaled and topical steroids are allowed)

• Planned administration or administration of a vaccine/product not foreseen by the study protocol during the Exclusion:

• Use of any investigational or non-registered product (drug or vaccine) other than the study vaccines/placebo during the period starting 30 days preceding the first dose of study vaccine/placebo and/or planned use during the study period

• Chronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting 180 days prior to the first vaccine/placebo dose (for corticosteroids, this will mean prednisone = 20 mg/day or equivalent; inhaled and topical steroids are allowed)

• Planned administration or administration of a vaccine/product not foreseen by the study protocol during the period starting 30 days prior to the first dose of vaccine/placebo until after the visit at Day 56 (if influenza activity warrants vaccination of healthy young adults, influenza vaccination will be encouraged and will not lead to study exclusion)

• Previous or planned administration of any other flavivirus vaccine (approved or investigational) for the entire study duration

• Previous receipt of any investigational dengue virus vaccine

• Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product (pharmaceutical product or device).

• Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination (no laboratory testing required).

• Family history of congenital or hereditary immunodeficiency

• History of, or current auto-immune disease

• History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine/placebo or related to a study procedure

• Major congenital defects or serious chronic illness

• History of any neurological disorders or seizures

• Acute disease and/or fever (=37.5°C/99.5°F oral body temperature) at the time of enrollment (a subject with a minor illness, i.e., mild diarrhea, mild upper respiratory infection, etc., without fever, may be enrolled at the discretion of the investigator)

• Acute or chronic, clinically significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by physical examination or laboratory screening tests

• Administration of immunoglobulins and/or any blood products during the period starting 90 days preceding the first dose of study vaccine/placebo or planned administration during the study period

• History of chronic alcohol consumption and/or drug abuse

• Pregnant or lactating female or female planning to become pregnant or planning to discontinue contraceptive precautions

• A planned move to a location that will prohibit participating in the trial until study end for the participant

• Any other condition which, in the opinion of the investigator, prevents the subject from participating in the study.

• Subject seropositive for hepatitis B surface antigen (HBsAg), hepatitis C virus antibodies (anti-HCV), or human immunodeficiency virus antibodies (anti-HIV)

• Safety laboratory test results that are outside the normal limits for their age, gender, and locality at screening.

Related Conditions & MeSH terms

• Dengue
• Dengue Fever

Intervention

Biological:
• Biological/Vaccine: 4 µg TDENV-PIV with Alum adjuvant

• Biological/Vaccine: 1 µg TDENV-PIV with AS03B adjuvant

Other:
• Phosphate buffered saline

Biological:
• 1 µg TDENV-PIV with Alum adjuvant

• 1 µg TDENV-PIV with AS01E adjuvant

Locations

Country	Name	City	State
Puerto Rico	Clinical Research Center, 1st Floor University Hospital	San Juan

Sponsors (3)

Lead Sponsor	Collaborator
U.S. Army Medical Research and Materiel Command	GlaxoSmithKline, Walter Reed Army Institute of Research (WRAIR)

Country where clinical trial is conducted

Puerto Rico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and reactogenicity of various TDENV-PIV formulations from Day 0 through 28 days after the second dose (Day 0 - Day 56)	Safety and Reactogenicity: Occurrence, intensity and relationship to vaccination of solicited local and general adverse events (AEs) during the 7-day follow-up period post each vaccination (Day 0-6); Occurrence, intensity and relationship to vaccination of unsolicited AEs during the 28-day follow-up period post each vaccination (Day 0-27); Hematological and biochemical levels at study visits on Days 0, 7, 28, 35 and 56; Occurrence of serious adverse events (SAEs) from Day 0 to Day 56; Occurrence of potential immune-mediated diseases (pIMDs) and medically attended AEs from Day 0 to Day 56	Up to Day 56
Primary	Humoral immunogenicity to each of four DENV types of various TDENV-PIV formulations 28 days after the second dose (Day 56)	Humoral Immunogenicity: Neutralizing antibody titers specific to each DENV type at Day 56; Geometric mean titers (GMTs) of neutralizing antibody titers to each DENV type; Rate of fold increases in neutralizing antibody from Day 0 for each DENV type; Seropositivity rates for each DENV type; Trivalent and tetravalent seropositivity rates	Day 56
Secondary	Safety of various TDENV-PIV formulations, from Day 0 to Month 13 (Visits 1-11)	Safety: Hematological and biochemical levels at study visits on Months 4, 7, 10 and Month 13; Occurrence of pIMDs and medically attended AEs from Day 0 to Month 13; Occurrence of any SAE from Day 0 to Month 13	Up to month 13
Secondary	Humoral immunogenicity to each of four DENV types of various TDENV-PIV formulations on Days 0, 7 and 28 and Months 7 and 13	Humoral Immunogenicity: Geometric mean titers (GMTs) of neutralizing antibody titers to each DENV type; Rate of fold increases in neutralizing antibody from Day 0 for each DENV type; Seropositivity rates for each DENV type; Trivalent and tetravalent seropositivity rates	Up to month 13
Secondary	• To evaluate the safety of various TDENV-PIV formulations from Month 14 through the end of the study (Visit 15)	Occurrence of serious adverse events (SAEs) related to study procedures from Month 14 to end of study (Month 37-39)	Up to the end of study (Month 37-39)