TDENV PIV and LAV Dengue Prime-boost Strategy

NCT ID: NCT02239614

Last Updated: 2018-08-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-12-31
• Study Completion Date: 2017-02-17

Brief Summary

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.

Conditions

Dengue

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Group 1: LAV (T=0), PIV (T=28)

Tetravalent live-attenuated dengue virus vaccine formulation 17 (TDENV-LAV) reconstituted with 0.7 mL of water-for-injection; administered subcutaneously on day 0 of the study.

Tetravalent dengue purified inactivated vaccine 4 μg/serotype with alum adjuvant (TDENV-PIV 4 µg + alum adjuvant) administered intramuscularly on day 28 of the study.

Group Type: EXPERIMENTAL

TDENV-LAV

Intervention Type: BIOLOGICAL

0.5 mL of the post-transfection LAV F17 vaccine

TDENV-PIV 4 µg + alum adjuvant

Intervention Type: BIOLOGICAL

0.5 mL of DENV serotypes 1-4 (4 µg / serotype) in alum adjuvant

Group 2: PIV (T=0), LAV (T=28)

Tetravalent dengue purified inactivated vaccine 4 μg/serotype with alum adjuvant (TDENV-PIV 4 µg + alum adjuvant) administered intramuscularly on day 0 of the study.

Tetravalent live-attenuated dengue virus vaccine formulation 17 (TDENV-LAV) reconstituted with 0.7 mL of water-for-injection; administered subcutaneously on day 28 of the study.

Group Type: EXPERIMENTAL

TDENV-LAV

Intervention Type: BIOLOGICAL

0.5 mL of the post-transfection LAV F17 vaccine

TDENV-PIV 4 µg + alum adjuvant

Intervention Type: BIOLOGICAL

0.5 mL of DENV serotypes 1-4 (4 µg / serotype) in alum adjuvant

Group 3: LAV (T=0), PIV (T=180)

Tetravalent live-attenuated dengue virus vaccine formulation 17 (TDENV-LAV) reconstituted with 0.7 mL of water-for-injection; administered subcutaneously on day 0 of the study.

Tetravalent dengue purified inactivated vaccine 4 μg/serotype with alum adjuvant (TDENV-PIV 4 µg + alum adjuvant) administered intramuscularly on day 180 of the study.

Group Type: EXPERIMENTAL

TDENV-LAV

Intervention Type: BIOLOGICAL

0.5 mL of the post-transfection LAV F17 vaccine

TDENV-PIV 4 µg + alum adjuvant

Intervention Type: BIOLOGICAL

0.5 mL of DENV serotypes 1-4 (4 µg / serotype) in alum adjuvant

Group 4: PIV (T=0), LAV (T=180)

Tetravalent dengue purified inactivated vaccine 4 μg/serotype with alum adjuvant (TDENV-PIV 4 µg + alum adjuvant) administered intramuscularly on day 0 of the study.

Tetravalent live-attenuated dengue virus vaccine formulation 17 (TDENV-LAV) reconstituted with 0.7 mL of water-for-injection; administered subcutaneously on day 180 of the study.

Group Type: EXPERIMENTAL

TDENV-LAV

Intervention Type: BIOLOGICAL

0.5 mL of the post-transfection LAV F17 vaccine

TDENV-PIV 4 µg + alum adjuvant

Intervention Type: BIOLOGICAL

0.5 mL of DENV serotypes 1-4 (4 µg / serotype) in alum adjuvant

Interventions

TDENV-LAV

0.5 mL of the post-transfection LAV F17 vaccine

Intervention Type: BIOLOGICAL

TDENV-PIV 4 µg + alum adjuvant

0.5 mL of DENV serotypes 1-4 (4 µg / serotype) in alum adjuvant

Intervention Type: BIOLOGICAL

Other Intervention Names

TDENV-LAV F17; Tetravalent dengue live attenuated virus formulation 17; Tetravalent dengue virus purified inactivated vaccine with alum adjuvant

Eligibility Criteria

Inclusion Criteria

1. Male or female between 18 and 49 years of age (inclusive) at the time of consent

2. Able to provide written informed consent

3. Healthy as established by medical history and clinical examination before entering into the study

4. Able and willing to comply with the requirements of the protocol (eg, document events in memory aid, return for follow-up visits, etc.)

5. 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)

6. Female subject is not breastfeeding and agrees not to breastfeed for 3 months after last vaccination

7. Female subject of childbearing potential may be enrolled in the study, if the subject has:

1. Practiced adequate contraception for 30 days prior to vaccinations, and

2. A negative urine pregnancy test on each day of vaccination, and

3. Agreed to continue adequate contraception until 3 months after completion of the vaccination series.

Exclusion Criteria

1. 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

2. 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

1. For corticosteroids, this will mean prednisone ≥ 20 mg/d or equivalent

2. Inhaled and topical steroids are allowed

3. 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

4. Planned administration of any flavivirus vaccine for the entire study duration

5. 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)

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

7. Family history of congenital or hereditary immunodeficiency

8. History of, or current, auto-immune disease

9. History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine or related to a study procedure

10. Major congenital defects or serious chronic illness

11. History of any neurological disorders or seizures. (except for a childhood febrile seizures)

12. 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)

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

14. 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

15. History of chronic alcohol and/or drug abuse

16. Pregnant or breastfeeding female or female planning to become pregnant or planning to discontinue contraceptive precautions

17. A planned move to a location that will prohibit participating in the trial prior to the study end for the participant

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

19. Safety laboratory test results that are outside the acceptable values at screening:

1. > 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)

2. < 100% lower limit of normal (LLN) or > 120% ULN for hemoglobin, hematocrit and platelet count

3. < 75% LLN or >110% ULN for total white blood cell count (WBC)

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 49 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

U.S. Army Medical Research and Development Command

FED

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

MAJ Leyi Lin, MD

Role: PRINCIPAL_INVESTIGATOR

Walter Reed Army Institute of Research (WRAIR)

Locations

Clinical Trials Center, Walter Reed Army Institute of Research (CTC, WRAIR)

Silver Spring, Maryland, United States

Countries

United States

References

Lin L, Koren MA, Paolino KM, Eckels KH, De La Barrera R, Friberg H, Currier JR, Gromowski GD, Aronson NE, Keiser PB, Sklar MJ, Sondergaard EL, Jasper LE, Endy TP, Jarman RG, Thomas SJ. Immunogenicity of a Live-Attenuated Dengue Vaccine Using a Heterologous Prime-Boost Strategy in a Phase 1 Randomized Clinical Trial. J Infect Dis. 2021 May 28;223(10):1707-1716. doi: 10.1093/infdis/jiaa603.

Reference Type: DERIVED

PMID: 32966573 (View on PubMed)

Other Identifiers

ADVP-003

Identifier Type: OTHER

Identifier Source: secondary_id

WRAIR #2136

Identifier Type: OTHER

Identifier Source: secondary_id

S-13-10

Identifier Type: -

Identifier Source: org_study_id