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CDSCO Approves Qdenga: India's First Dengue Vaccine to be Distributed by Dr Reddy's from 2027

Target:UPSC GS-IIIMPSCTeachingSSC GAPrelims HighMains MediumStatic GK Link
18 Sept 2026
~2 min
Source: Indian Express
Key Data:July 2026ages 4 to 6061.2% efficacy84.1% hospitalization2 doses3 months apart
Bodies:CDSCOTakeda Pharmaceutical CompanyDr Reddy's LaboratoriesWHO
Practice MCQs from today's news ▸
What This Article Covers

1.Qdenga, developed by Takeda, is India’s first approved dengue vaccine. CDSCO granted marketing authorisation in July 2026 for ages 4-60.

2.Two-dose regimen (0.5 mL subcutaneous, 3 months apart). No pre-vaccination screening needed – a key advantage over earlier vaccines.

3.Dr Reddy’s will exclusively distribute in the private market from H1 2027. Inclusion in Universal Immunization Programme remains a long-term ambition.

The Big Picture
Prelims · HighMains · Medium

India’s first approved dengue vaccine Qdenga will enter the private market in 2027 via Dr Reddy’s, after CDSCO approval in July 2026. The vaccine is effective against all four serotypes, requires no pre-vaccination screening, and shows 61.2% efficacy against dengue and 84.1% against hospitalization. This is a landmark step in India's fight against dengue.

Exam Lens

Quick Exam Facts From News

Vaccine NameQdenga (by Takeda)
Approval AuthorityCDSCO (July 2026)
Age Group4 to 60 years
Efficacy – Dengue61.2%
Efficacy – Hospitalisation84.1%
Dose Regimen2 doses, 3 months apart
Distribution PartnerDr Reddy’s Laboratories
Market LaunchPrivate market, H1 2027
Global StatusApproved in 43 countries, WHO prequalified

1-Minute Revision

  • ›Vaccine Name: Qdenga (by Takeda)
  • ›Approval Authority: CDSCO (July 2026)
  • ›Target this Data: Qdenga efficacy: 61.2% against dengue, 84.1% against hospitalisation; age group 4-60; 2 doses 3 months apart.
  • ›Target this Nodal Body: CDSCO (Central Drugs Standard Control Organisation) – approved Qdenga in July 2026.
  • ›Target this Legal Point: Marketing authorisation vs. commercial launch; requires Registration Certificate and Import Licence.

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Q1Static LinkageEasy

Which regulatory body granted marketing authorisation to India's first dengue vaccine Qdenga?

Q2Statement-basedHard

Consider the following statements regarding Qdenga dengue vaccine:

1. Qdenga is a live attenuated tetravalent vaccine using DENV-2 as its backbone.

2. The vaccine requires pre-vaccination screening to check for prior dengue infection.

3. Clinical trials showed 84.1% efficacy against dengue-related hospitalisation at 4.5 years.

Which of the statements given above is/are correct?

Q3Data-centricMedium

According to the article, what is the recommended interval between the two doses of Qdenga?

Q4Application/ImpactMedium

Why is the absence of pre-vaccination screening a significant advantage for Qdenga in the Indian context?

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