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Takeda’s Qdenga (dengue tetravalent vaccine) Receive BPOM’s Approval for the Prevention of Dengue Disease in Indonesia

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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

Click here to­ read the full press release 

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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