A Study on the Epidemiology and Testing of Human Epidermal Growth Factor-Receptor 2 (HER2) in Breast Cancer in Germany

  • Cancer
  • Breast Cancer
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Completed

This trial runs in
Country
  • Germany
Trial Identifier:

NCT02666261 ML29763

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      This non-interventional study will collect data from routine diagnostics on HER2 testing of breast cancer in Germany.

      Hoffmann-La Roche Sponsor
      N/A Phase
      NCT02666261, ML29763 Trial Identifier
      Breast Cancer Condition
      Official Title

      A Non-interventional Study on the Epidemiology and Testing of HER2 in Breast Cancer in Germany

      Eligibility Criteria

      All Gender
      ≥ 18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Samples derived from men and women of age greater than or equal to (>/=) 18 years
      • Samples derived from participants with any stage of histologically confirmed invasive breast cancer with HER2 diagnostics performed within routine (histo-)pathological workup or
      • (Histo-)Pathological work-up of the tumor sample as at or after start of this study
      • Available information on the year of birth of the participant
      • No pre-selection of tumor samples is allowed. Tumor samples have to be documented consecutively in the order of their (histo-)pathological work-up.
      Exclusion Criteria
      • Sample derived from participants with any stage of breast cancer with no HER2 diagnostics performed at the time of routine (histo-)pathological work-up.
      • Samples derived prior to the start of this study.

      For the latest version of this information please go to www.forpatients.roche.com

       

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