Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT02834637 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

A Dose Reduction Immunobridging and Safety Study of Two HPV Vaccines in Tanzanian Girls

Study acronym: DoRIS
StatusActive, Not Recruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Collaborators revised (7)v12
  2. Minor Publications: 7 to 8v11
  3. Minor Publications: 5 to 7v10
  4. Minor Re-verified, no change to tracked fieldsv9
  5. Minor Study completion date: Mar 2024 to Mar 2027
    • Secondary endpoints: 15 to 14
    • Study description expanded, about 1 word
    v8
Show 6 earlier versionsHide 6 earlier versions
  1. Notable Primary endpoints: 2 to 3
    • Study completion date: Mar 2021 to Mar 2024
    • Secondary endpoints: details revised at 2 of 15 entries
    • Study description expanded, about 51 words
    v7
  2. Minor Primary completion date changed from estimate of Nov 2020 to Jan 15, 2020v6
  3. Minor Re-verified, no change to tracked fieldsv5
  4. Notable Primary endpoints: 3 to 2v4 Show 4 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 900 to confirmed 930
    • Secondary endpoints: 16 to 15
    • Site details revised
  5. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Start date: Aug 2016 to Feb 23, 2017
    • Study sites: 0 to 1
    • Primary completion date: May 2020 to Nov 2020
    • Study completion date: Aug 2020 to Mar 2021
  6. Minor Re-verified, no change to tracked fieldsv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Cervical cancer is the most common cancer in women aged 15-44 years in East Africa, and mortality rates are very high. HPV vaccines are most effective if given to girls who have not yet acquired HPV infection. In Tanzania, HPV vaccine has been shown to be safe, acceptable and can be delivered with high coverage (\~80%). However, the cost of delivering HPV vaccine is considerably higher than costs for traditional infant/child vaccinations. This is primarily because of costs to establish outreach programmes and associated personnel costs including nurses who must spend significant time away from their posts to deliver vaccine, especially if multiple doses are needed. There is global interest in simplifying HPV vaccine delivery by reducing the number of doses. If a single dose could be given, this could halve the costs of delivery, making it more accessible to the populations that need it most. Recently, the WHO recommended that 2 doses of HPV vaccine could be given to young girls, based on studies in high and upper middle-income countries. However in Africa high rates of infections like malaria and worms can affect immune responses to vaccines. It is essential to know that reducing the number of doses does not reduce the protective immune response of these vaccines. The investigators are conducting a trial in Tanzanian girls aged 9-14 years to establish whether a single dose of HPV vaccine produces immune responses that are likely to be effective in preventing cervical cancer. Two different HPV vaccines, the bivalent (2-v) vaccine that protects against HPV 16/18 (the cause of 70% of cancers) and the 9-valent (9-v) vaccine that protects against 9 HPV types, will be compared. The trial will randomise 900 girls to 6 arms and follow them for 36 months. Girls will receive the 2-v or the 9-v HPV vaccine, as 1, 2 or 3 doses. Girls receiving 1 or 2 doses will be compared with those receiving 3 doses of the same vaccine, to ensure that the reduced dose regimen produces an immune response that is not inferior to 3 doses. Girls in the 1 and 2 dose arms will be enrolled in an extension and followed for up to 9 years, to examine the stability of immune responses. The immune responses in this study will also be compared with results from other countries where the vaccine has been shown to be protective. This will provide information about whether a reduced number of doses is likely to be protective in Africa. This work will be extremely important in informing future HPV vaccination strategies and will be one of the first randomised trials of 1 and 2 doses of any HPV vaccine in Africa.
Trial Details
NCT Number NCT02834637
Lead Sponsor London School of Hygiene and Tropical Medicine
Collaborators: University of York, Institut Català d'Oncologia, National Cancer Institute (NCI), Karolinska Institutet, Technische Universität Berlin, Tanzanian National Institute for Medical Research, University of Glasgow
Conditions
(from sponsor)
Human Papilloma Virus
Related terms Uterine Cervical Neoplasms
Enrollment 930 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov