S-AVANT observational study follow up

  • Research type

    Research Study

  • Full title

    S-AVANT. Follow-up to the AVANT study up to 8 and 10 years (median follow-up) in patients with colon carcinoma.

  • IRAS ID

    210852

  • Contact name

    Nelly Roldan

  • Contact email

    nelly.roldan@gercor.com.fr

  • Sponsor organisation

    GERCOR

  • Clinicaltrials.gov Identifier

    NCT02228668

  • Clinicaltrials.gov Identifier

    NCT02228668, www.clinicaltrials.gov

  • Duration of Study in the UK

    0 years, 3 months, 21 days

  • Research summary

    This is a follow-up study of participants previously randomised in the AVANT study at 8 and 10 years median follow-up. No visits to the study site, and no assessments or clinical examinations are required as data will be obtained from the medical notes of those participants who were randomised into the previous AVANT study. Data will be collected for: Date of last contact/follow-up; date and type of first relapse, first treatment of metastatic disease (chemotherapy and local treatment), date and type of other cancer, biomarkers and adverse events occurred after AVANT database lock (31 Aug 2012) and related to bevacuzimab or capecitabine administered in the AVANT study; survival status (alive or deceased).

  • REC name

    West Midlands - Edgbaston Research Ethics Committee

  • REC reference

    17/WM/0290

  • Date of REC Opinion

    20 Sep 2017

  • REC opinion

    Further Information Favourable Opinion