Clinical Trial of the Safety and Immunogenicity of a Tetravalent Dengue Virus Vaccine Admixture TV005 in the Elderly Aged 50-70 Years in Taiwan

NCT04133987 | Completed Phase 2 DMC

• 1 other identifier: 201712180MSD
• Study Type: interventional
• Target: 252
• Locations: 1 country
• Sites: 1

Brief Summary

Phase II, randomized, double-blind, placebo-controlled study of the safety and immunogenicity of the recombinant live attenuated tetravalent dengue virus vaccine admixture TV005 in the elderly in Taiwan

Conditions

Dengue

Keywords

tetravalent dengue vaccine; Phase II clinical trial

Outcome Measures

Primary Outcomes (4)

• Proportion of study participants with solicited local and general adverse events.

  Measured through Day 21

• Proportion of study participants with unsolicited adverse events.

  Measured through Day 29

• Proportion of study participants with serious adverse events.

  Measured through Day 1080

• Evaluation of the immunogenicity of TV005, as assessed by PRNT50 to DENV-1, DENV-2, DENV-3, and DENV-4 at 28, 56, 72 and 180 days after TV005 vaccination

  Measured through Day 180

Secondary Outcomes (2)

• Evaluation of the frequency and quantity of viremia of each monovalent component of the vaccine after vaccination.

  Measured through Day 21

• Number of TV005 vaccinees infected with DENV-1, DENV-2, DENV-3, and DENV-4.

  Measured through Day 72

Study Arms (2)

Tetravalent live attenuated dengue vaccine admixture TV005

EXPERIMENTAL

Tetravalent live attenuated dengue vaccine admixture TV005

Biological: Tetravalent live attenuated dengue vaccine admixture TV005

placebo

PLACEBO COMPARATOR

Plasma-Lyte A

Biological: Placebo

Interventions

Tetravalent live attenuated dengue vaccine admixture TV005 BIOLOGICAL

The admixtures of the candidate vaccines each contain 4 live attenuated dengue viruses, each of a different serotype.

Tetravalent live attenuated dengue vaccine admixture TV005

Placebo BIOLOGICAL

PLASMA-LYTE A Injection pH 7.4 (Multiple Electrolytes Injection, Type 1, USP) is a sterile, nonpyrogenic isotonic solution in a single dose container for intravenous administration.

placebo

Eligibility Criteria

• Age: 50 Years - 70 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Man or non-pregnant / non-lactating woman between the ages of 50 years and 70 years at the time of enrollment into the study.
• 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).
• Subject who allows to access to their Medical Record.
• Subjects whose residence is in Taiwan who will remain available for the duration of the study, approximately 3 years following the first vaccination.
• Good general health as determined by physical examination, laboratory screening, and review of medical history.
• An informed consent form signed and dated by the subject.
• If the subject is female, she must be of non-childbearing potential, i.e. surgically sterilized or one year post-menopausal; or, if of childbearing potential, she must be abstinent or have used adequate contraceptive precautions (i.e. intrauterine contraceptive device; condom and spermicide combination, oral contraceptives or other equivalent hormonal contraception, e.g. progestin implantable, cutaneous hormonal patch or injectable contraceptives) for 30 days prior to vaccination, have a negative pregnancy test prior to vaccination and must agree to continue such precautions for 90 days after completion of the vaccination. For male subject, he must be abstinent or use a condom together with spermicide for 14 days after completion of the vaccination.

You may not qualify if:

• Pregnant or lactating female or female planning to become pregnant within 90 days of receiving an investigational product or planning to discontinue abstinence or contraceptive precautions within 90 days of receiving an investigational product.
• Acute or chronic, clinically significant neurological, pulmonary, cardiovascular, hepatic, renal, autoimmune, hematologic, endocrine disease or functional defect, as determined by history, physical examination or screening tests that in the opinion of the investigator would, will jeopardize the safety or rights of a subject participating in the trial or would render the subject unable to comply with the protocol.
• Psychiatric, behavioral disorder, or seizures (with the exception of a single febrile seizure in childhood) that in the opinion of the investigator, will affect the ability of the subject to understand and cooperate with the requirements of the study protocol.
• Self-reported or suspected congenital or acquired immunodeficiency, or asplenia; or receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within the preceding 6 months, or long-term systemic corticosteroid therapy (prednisone or equivalent, ≥ 0.5 mg/kg/day or 20 mg/day, for more than 2 consecutive weeks within the past 3 months). Inhaled and topical steroids are allowed.
• HIV infection by screening (by HIV Ag/Ab combo test or HIV Ab test) and confirmatory assays (by Western blot), Hepatitis C virus (HCV) infection by Anti-HCV antibody, or Hepatitis B virus (HBV) infection by Hepatitis B surface antigen (HBsAg) screening or, unwilling to allow HIV, HCV and HBV testing.
• Screening laboratory values of hemoglobin \<9.5 gm/dL in female adults or \<11 gm/dL in male adults, neutrophil \<1,000 mm3, platelet \< 100,000/mm3, Creatinine \>1.5 mg/dL, Bilirubin-T \>1.5 times of upper limit, or ALT \> 2 times of upper limit.
• History of allergic disease/reaction likely to be exacerbated by any component of the vaccine, or any history of a severe allergic reaction or anaphylaxis.
• Current alcohol abuse or drug addiction that might interfere with the ability to comply with trial procedures.
• Any other condition that in the opinion of the investigator would jeopardize the safety or rights of a subject participating in the trial or would render the subject unable to comply with the protocol.
• Planned administration of any vaccine not foreseen by the study protocol, during the period starting from 30 days before the study vaccine and ending 30 days after study vaccination; with the exceptions of the inactivated influenza vaccine or the inactivated rabies vaccine (without administration of immunoglobulin) administered.
• Use of any investigational or non-registered drug or vaccine other than the study vaccine within 30 days preceding the study vaccine/placebo or planned use at any time during the study period or history of having received any investigational dengue vaccine at any previous time.
• Administration of immunoglobulins and/or blood products within 90 days preceding the study vaccine dose or planned administration at any time during the study period, which might interfere with assessment of the immune response. Or administration of killed vaccine within 14 days, or attenuated vaccine within 28 days.
• A planned or anticipated move to a location that will prohibit participating in the trial for the 12-month duration and unavailable for schedule visit during 2nd and 3rd year follow-up.
• Potential volunteers who do not have easy access to a fixed or mobile telephone.
• Any subject identified as a site employee of the Investigator or study clinic, with direct involvement in the proposed study or other studies under the direction of that Investigator or study clinic, as well as any family member (i.e., immediate, husband, wife and their children, adopted or natural) of the clinic employees or the Investigator.

Sponsors & Collaborators

• National Taiwan University Hospital: lead
• Centers for Disease Control, Taiwan: collaborator

Study Sites (1)

National Taiwan University Hospital

Taipei, 100, Taiwan

Location

MeSH Terms

Conditions

Dengue

Condition Hierarchy (Ancestors)

Mosquito-Borne Diseases; Vector Borne Diseases; Infections; Arbovirus Infections; Virus Diseases; Flavivirus Infections; Flaviviridae Infections; RNA Virus Infections; Hemorrhagic Fevers, Viral

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: INVESTIGATOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 23, 2019
• First Posted: October 21, 2019
• Study Start: October 15, 2018
• Primary Completion: April 30, 2020
• Study Completion: September 30, 2022
• Last Updated: January 18, 2023

Record last verified: 2023-01

Locations

TW (1)