Trial Profile
A Randomized, Observer Blind, Phase 3 Trial to Investigate the Immunogenicity and Safety of the Co-administration of a Subcutaneous Tetravalent Dengue Vaccine Candidate (TDV) and an Intramuscular Hepatitis A Virus (Inactivated) Vaccine in Healthy Subjects Aged 18 to 60 Years in Non-endemic Country(Ies) for Dengue
Status:
Completed
Phase of Trial:
Phase III
Latest Information Update: 25 Jan 2023
Price :
$35
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At a glance
- Drugs Hepatitis A vaccine (Primary) ; TAK 003 (Primary)
- Indications Dengue; Hepatitis A
- Focus Pharmacodynamics; Registrational
- Sponsors Takeda
- 19 Jan 2023 Results assessing safety and immunogenicity of coadministration of TAK-003 in healthy adults aged 18-60 years living in the UK, published in the Vaccine.
- 12 Jul 2019 Status changed from active, no longer recruiting to completed.
- 25 Jun 2019 Planned End Date changed from 11 Jun 2019 to 10 Jul 2019.