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NCT03900572

A Study of Safety and Primary Immunogenicity of 9-valent HPV Recombinant Vaccine

Completed Phase 1 Last updated 13 April 2023
What this trial tests

Phase 1 trial testing HPV Vaccine in HPV Infections in 90 participants. Completed in 30 April 2020.

Timeline
9 March 2019
Primary endpoint
30 April 2020
30 April 2020

Quick facts

Lead sponsorShanghai Zerun Biotechnology Co.,Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment90
Start date9 March 2019
Primary completion30 April 2020
Estimated completion30 April 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Zerun Biotechnology Co.,Ltd — full company profile →

Who can join

Adults 9 to 45, female only, with HPV Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A randomized, double-blind and placebo-controlled phase I study to evaluate the safety and immunogenicity of a 9-valent Human Papillomavirus (HPV) vaccine, administered intramuscularly according to a 0, 2, 6-month schedule in 9 to 45 years old healthy Chinese females.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of HPV Vaccine

Trials testing the same drug.

Other recruiting trials for HPV Infections

Currently open trials in the same condition.

Other Shanghai Zerun Biotechnology Co.,Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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