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RECRUITING
NCT06388785

A Study to Monitor the Adverse Events of QDENGA Vaccine in Participants in Malaysia

Sponsor: Takeda

View on ClinicalTrials.gov

Summary

The main aim of this study is to collect the number and type of medical problems (adverse events) after vaccination with QDENGA in Malaysia and to learn more about such medical problems after vaccination. Another aim of this study is to collect the number of persons vaccinated with QDENGA who need to stay in the hospital because of severe dengue fever. No vaccination will be given as part of this study. The study will only collect data of persons already vaccinated with QDENGA who agree to participate.

Official title: Post-vaccination Surveillance for Monitoring the Adverse Events Following Immunisation With QDENGA in a Real-world Setting in Malaysia (PRIME-Q)

Key Details

Gender

All

Age Range

4 Years - Any

Study Type

OBSERVATIONAL

Enrollment

2000

Start Date

2024-09-26

Completion Date

2027-05-08

Last Updated

2025-06-12

Healthy Volunteers

Yes

Conditions

Interventions

OTHER

No Intervention

This is a non-interventional study.

Locations (2)

Universiti Malaya

Kuala Lumpur, Kuala Lumpur, Malaysia

Universiti Putra Malaysia

Serdang, Selangor, Malaysia