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Clinical trial

A Randomized, Active Controlled, Assessors-blind Trial to Establish Non-inferiority of Immunogenicity of a Single-dose of CERVAVAC® Quadrivalent HPV Vaccine Compared to the Gardasil® Quadrivalent Vaccine Among Girls and Boys Aged 9 to 14 Years and in Girls/Women Aged 15 to 20 Years in Zambia

NCT07256912 is registered in ClinicalTrials.gov with International Agency for Research on Cancer as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Active Controlled, Assessors-blind Trial to Establish Non-inferiority of Immunogenicity of a Single-dose of CERVAVAC® Quadrivalent HPV Vaccine Compared to the Gardasil® Quadrivalent Vaccine Among Girls and Boys Aged 9 to 14 Years and in Girls/Women Aged 15 to 20 Years in Zambia
Lead sponsor
International Agency for Research on Cancer
Phase
Phase 4
Overall status
Active, not recruiting
Start date
June 1, 2026
Completion date
January 15, 2029
Enrollment
1,266 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

cervical cancer prevention, hpv vaccination, immunogenicity, quadrivalent hpv vaccine, single dose, vaccine effectiveness