TDENV PIV and LAV Dengue Prime-boost Strategy

Completed · Phase 1

Conditions studied: Dengue

In brief

The potential synergistic effect of administering 2 dengue vaccine candidates that were previously shown to be safe and immunogenic in humans will be evaluated in this study. A prime-boost study of tetravalent dengue virus purified inactivated vaccine (TDENV-PIV) with alum and tetravalent dengue live attenuated virus (TDENV-LAV) vaccine Formulation 17 (F17) will gather data to help better understand the human immune response to dengue vaccination and infection.

Key facts

Study ID

NCT02239614

Run by

U.S. Army Medical Research and Development Command

People needed

80

Starts

2014-12-01

Expected to finish

2017-02-17

Last updated by the study team

2018-08-15

Who can join

Age: 18 and older, up to 49. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female between 18 and 49 years of age (inclusive) at the time of consent
• Able to provide written informed consent
• Healthy as established by medical history and clinical examination before entering into the study
• Able and willing to comply with the requirements of the protocol (eg, document events in memory aid, return for follow-up visits, etc.)
• Female subject of non-childbearing potential (non-childbearing potential is defined as having either a current tubal ligation at least 3 months prior to enrollment or a history of a hysterectomy, ovariectomy, or is post-menopause)
• Female subject is not breastfeeding and agrees not to breastfeed for 3 months after last vaccination
• Female subject of childbearing potential may be enrolled in the study, if the subject has:
• Practiced adequate contraception for 30 days prior to vaccinations, and
• A negative urine pregnancy test on each day of vaccination, and
• Agreed to continue adequate contraception until 3 months after completion of the vaccination series.

You may not qualify if…

• Use of any investigational or non-registered product (drug or vaccine) other than the study vaccines during the period starting 30 days preceding the first dose of study vaccine 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 dose
• For corticosteroids, this will mean prednisone ≥ 20 mg/d 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 14 days before or after each scheduled dose of an investigational product
• Planned administration of any flavivirus vaccine for the entire study duration
• 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 or related to a study procedure
• Major congenital defects or serious chronic illness
• History of any neurological disorders or seizures. (except for a childhood febrile seizures)
• Acute disease and/or fever (oral body temperature ≥ 100.4°F/38.0°C) at the time of enrollment (a subject with a minor illness, ie, 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 or planned administration during the study period
• History of chronic alcohol and/or drug abuse
• Pregnant or breastfeeding 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 prior to the study end for the participant
• 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 acceptable values at screening:
• > 110% upper limit of normal (ULN) for alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase, creatinine, serum urea nitrogen (SUN) and bilirubin (total and direct)
• < 100% lower limit of normal (LLN) or > 120% ULN for hemoglobin, hematocrit and platelet count
• < 75% LLN or >110% ULN for total white blood cell count (WBC)
• Any other condition which, in the opinion of the investigator, prevents the subject from participating in the study.

Where it is running

• Clinical Trials Center, Walter Reed Army Institute of Research (CTC, WRAIR) — Silver Spring, Maryland, United States

Full record on ClinicalTrials.gov

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