Takeda’s Qdenga (dengue tetravalent vaccine) Receive BPOM’s Approval for the Prevention of Dengue Disease in Indonesia
Shots:
- BPOM has approved Qdenga for the prevention of dengue disease caused by any serotype in patients aged 6 to 45yrs. The therapy is expected to be available in the coming months
- The approval was based on an ongoing P-III (TIDES) trial to evaluate Qdenga in ~20000 healthy children & adolescents aged 4 to 16yrs. with dengue endemic across Asia & Latin America. The results showed continued overall protection against dengue illness & hospitalization @3yrs. after vaccination regardless of prior dengue exposure, was well tolerated with no safety risks
- Qdenga is currently under regulatory review for the prevention of dengue in children and adults in the EU and dengue-endemic countries outside the EU
Ref: Businesswire | Image: Takeda
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