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NCT01290393

Post-marketing Study to Assess the Safety of CERVARIX When Used in the United States and in Canada

Terminated Last updated 26 July 2018
What this trial tests

trial testing Data collection in Infections, Papillomavirus in 2 participants. Terminated before completion.

Timeline
26 September 2011
Primary endpoint
20 December 2012
20 December 2012

Quick facts

Lead sponsorGlaxoSmithKline
StatusTerminated
Study typeOBSERVATIONAL
Enrollment2
Start date26 September 2011
Primary completion20 December 2012
Estimated completion20 December 2012
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 15 to 25, female only, with Infections, Papillomavirus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will assess the risk of spontaneous abortion during weeks 1-19 of gestation, and other pregnancy outcomes, in an Exposed vaccinated cohort, i.e. women with last menstrual period between 30 days before and 90 days after any dose of CERVARIX, when compared to a Non-exposed vaccinated cohort, i.e. women with last menstrual period between 120 days and 18 months after the last CERVARIX or GARDASIL dose.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Data collection

Trials testing the same drug.

Other GlaxoSmithKline trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01290393.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing