Autopsy report · NCT02082639

Immunogenicity and Safety Study of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus Vaccine (Cervarix™) When Co-administered With GSK Biologicals' Hepatitis A Vaccine (Havrix®) in Healthy Female Adolescents Aged 9-14 Years

“Because the Russian Authorities already approved the 2-dose Cervarix™ schedule, the study was no longer needed for registration and hence it was cancelled.”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Phase

Phase 3

Sponsor

GlaxoSmithKline

Sponsor type

Industry

Conditions

Infections, Papillomavirus

Interventions

Cervarix™; Havrix

Participants

0

Trials that died the same way

• Clinical Efficacy of Intense Pulsed Light(IPL) Procedure in Dry Eye Patient
  “Due to the covid 19, patient recruiment is not going smoothly, so the study was canceled.” (65% match in meaning)
• A Study Of Safety, Tolerability And Effectiveness Of Recifercept In Children With Achondroplasia
  “The study was terminated due to lack of efficacy at any of the tested doses on 18th November 2022. The decision to terminate the study is not related to a safety concern.” (64% match in meaning)
• Real-Life Use of Transabdominal Restorelle® Meshes in Apical Prolapse Repair
  “From June 08, 2024, the study device was no longer marketed in France. Therefore, the sponsor decided to terminate the study prematurely.” (61% match in meaning)
• Study of a Birth Dose of GlaxoSmithKline Biologicals' 251154 Vaccine
  “Study was cancelled before enrolment for reasons not related to vaccine safety or efficacy.” (61% match in meaning)
• Study of Combination Therapy With LdT Plus Adefovir Versus Adefovir Alone
  “The study was not completed as planned and was terminated early with agreement from the European Medicines Agency (EMEA)” (61% match in meaning)

Look deeper

• The official registry record (the source of truth)
• Record history: every change the sponsor made
• Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.