Drug Use Investigation for Cervarix®

NCT01187927 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1230

Last updated 2015-01-26

No results posted yet for this study

Summary

This post-marketing study was designed to assess safety and efficacy of Cervarix® vaccine in Japanese female subjects under conditions of actual use.

Conditions

  • Infections, Papillomavirus

Interventions

BIOLOGICAL

Cervarix®

Administered according to the prescribing information in the locally approved label by the authorities.

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Min Age
10 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2014-01-31
Completion
2014-01-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01187927 on ClinicalTrials.gov