A Study of 2 Doses of Tetravalent Dengue Vaccine (TDV) in Infants and Toddlers

NCT ID: NCT06665035

Last Updated: 2025-07-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE3

Total Enrollment

212 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-16

Study Completion Date

2030-03-03

Brief Summary

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Dengue fever is caused by an infection with the dengue virus. Vaccination with Dengue Tetravalent Vaccine (TDV) can help prevent dengue fever. The purpose of this study is to collect information of vaccination with TDV when given to children younger than 2 years. The main aims of this study are to learn how safe the vaccine is and how well it works to activate a young child's immune system (this is called immunogenicity). Children between the age of 6 and 21 months will receive two vaccinations with either TDV or placebo 3 months apart. Blood samples will be taken before and after the vaccination as well as throughout the study. These are necessary to check how well the vaccine works to activate the immune system. During the study, participants will visit their study clinic 8 times for vaccinations, blood draws and health checks.

Detailed Description

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Conditions

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Dengue Fever

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Cohort 1: Tetravalent Dengue Vaccine (TDV) 0.5 mL (Age group: >=12 to <21 months)

Participants with the age group \>= 12 to \< 21 months receive TDV 0.5 mL subcutaneous (SC) injection, on Day 1 and Day 90.

Group Type EXPERIMENTAL

TDV

Intervention Type BIOLOGICAL

TDV SC injection.

Cohort 1: Placebo (Age group: >=12 to <21 months)

Participants with the age group \>= 12 to \< 21 months receive placebo (normal saline), SC injection, on Day 1 and Day 90.

Group Type EXPERIMENTAL

Placebo

Intervention Type OTHER

Placebo SC injection.

Cohort 2: TDV 0.5 mL(Age group: >=6 to <12 months)

Participants with the age group \>=6 to \<12 months receive TDV, 0.5 mL SC injection, on Day 1 and Day 90.

Group Type EXPERIMENTAL

TDV

Intervention Type BIOLOGICAL

TDV SC injection.

Cohort 2: Placebo (Age group: >=6 to <12 months)

Participants with the age group \>=6 to \<12 months receive placebo (normal saline), SC injection, on Day 1 and Day 90.

Group Type EXPERIMENTAL

Placebo

Intervention Type OTHER

Placebo SC injection.

Interventions

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TDV

TDV SC injection.

Intervention Type BIOLOGICAL

Placebo

Placebo SC injection.

Intervention Type OTHER

Other Intervention Names

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QDENGA TAK-003

Eligibility Criteria

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Inclusion Criteria

Participant eligibility is determined according to the following criteria:

1. Participant is aged \>=6 to \<21 months at the time of entry into the trial.
2. Participant is male or female.
3. Participant is in good health at the time of entry into the trial as determined by medical history, physical examination (including vital signs), and the clinical judgment of the investigator.
4. Participant's legally acceptable representative (LAR) has signed and dated a written informed consent form (ICF) and any required privacy authorization prior to the initiation of any trial procedure, and after the nature of the trial has been explained according to local regulatory requirements.
5. The participant and participant's LAR can comply with trial procedures and can be available for the duration of follow-up, according to the LAR.

Exclusion Criteria

Any participant who meets any of the following criteria will not qualify for randomization:

1. Participant has contraindication(s), warning(s) and/or precaution(s) applicable to vaccination with TDV as specified in the investigator's brochure (IB)and/or the approved product label (as applicable) in the participating country.
2. Participant has a known hypersensitivity or allergy to any of the investigational medicinal product (IMP) components (including excipients).
3. Participant has behavioral or cognitive impairment or psychiatric disease that, in the opinion of the investigator, may interfere with the participant's ability to participate in the trial.
4. Participant has a history of progressive or severe neurologic disorder, seizure disorder or neuro-inflammatory disease (example, Guillain-Barré syndrome).
5. Participant has an illness, or history of any illness that, in the opinion of the investigator, might interfere with the results of the trial or pose additional risk to the participant due to involvement in this trial.
6. Participant has a known or suspected impairment/alteration of immune function, including:

1. Chronic administration of oral and/or parenteral steroids at doses considered sufficiently immunosuppressive (example, \>=2 mg/kg \[milligrams per kilograms\] body weight/day prednisone \[or equivalent\] for 14 consecutive days, or, \>=20 milligram per day \[mg/day\] prednisone \[or equivalent\] for \>=14 consecutive days) within 60 days prior to Day 1 month 0 (M0) (note: use of corticosteroids by inhaled, intranasal, intraarticular, bursal, tendon injection, or topical routes is allowed).
2. Receipt of blood, immunoglobulins, blood products, and/or plasma derivatives within the 3 months prior to Day 1 (M0).
3. Receipt of immunostimulants within 60 days prior to Day 1 (M0).
4. Immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within 6 months prior to Day 1 (M0).
5. HIV infection or HIV-related disease.
6. Hepatitis B virus infection.
7. Hepatitis C virus infection.
8. Genetic immunodeficiency.
7. Participant has known or suspected abnormalities of splenic or thymic function.
8. Participant has a known bleeding diathesis, or any condition/medication that may be associated with a prolonged bleeding time.
9. Participant has a serious chronic or progressive disease deemed to be preclusive to trial entry, that is., not medically stable according to the judgment of the investigator.
10. Participant has previously received a vaccination against dengue virus (investigational or licensed).
11. Participant has a clinically significant active infection (as assessed by the investigator) or body temperature greater than (\>) 38.0 degrees Celsius (°C) (\>100.4 degrees Fahrenheit \[°F\]) within 3 days of intended IMP administration on Day 1 (M0).
12. Participant has used antipyretics and/or analgesic medications within 24 hours prior to vaccination. The reason for their use (prophylaxis vs treatment) must be documented. Trial entry must be delayed to allow for a full 24 hours to have passed since last use of antipyretics and/or analgesic medications.
13. Participant has received any of the following:

1. A licensed vaccine within 14 days (for inactivated vaccines) or 28 days (for live vaccines) prior to IMP administration on Day 1 (M0). This includes co-administration with routine vaccines.
2. A coronavirus vaccine within 14 days prior to IMP administration on Day 1 (M0).
3. A vaccine authorized for emergency use within 28 days prior to IMP administration on Day 1 (M0).
14. Participant is scheduled to receive any other vaccine within 28 days after IMP administration on Day 1 (M0).
15. Participant is participating in any clinical trial with another investigational product 30 days prior to Day 1 (M0) or plans to participate in another clinical trial at any time during the conduct of this trial.
16. Participant has taken part in any clinical trial of a dengue or other flavivirus (example, West Nile virus) candidate vaccine, except if it is known that the participant received placebo in the trial(s).
17. A first degree relative is involved in the conduct of this trial.
Minimum Eligible Age

6 Months

Maximum Eligible Age

20 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Takeda

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Study Director Study Director

Role: STUDY_DIRECTOR

Takeda

Locations

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Clinica de la Costa Ltda

Barranquilla, Atlántico, Colombia

Site Status NOT_YET_RECRUITING

Centro de Estudios en Infectologia Pediatrica S.A.S

Cali, Valle del Cauca Department, Colombia

Site Status NOT_YET_RECRUITING

King Chulalongkorn Memorial Hospital

Pathum Wan, Bangkok, Thailand

Site Status NOT_YET_RECRUITING

Thammasat University Hospital

Khlong Luang, Changwat Pathum Thani, Thailand

Site Status RECRUITING

Countries

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Colombia Thailand

Central Contacts

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Takeda Contact

Role: CONTACT

+1-877-825-3327

Facility Contacts

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Site Contact

Role: primary

+573 157-6091 ext. 10

Site Contact

Role: primary

+572 513-3762

Site Contact

Role: primary

+66 8 948-18922

Site Contact

Role: primary

+66 2 926-9514

Other Identifiers

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2023-001084-54

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

DEN-306

Identifier Type: -

Identifier Source: org_study_id

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