A Study to Describe the Diagnosis, Anti-Cancer Treatment and Clinical Outcome in Patients With Newly Diagnosed Breast Cancer in Latin America

  • Cancer
  • Breast Cancer
Please note that the recruitment status of the trial at your site may differ.
Trial Status:

Active, not recruiting

This trial runs in
Cities
  • Barranquilla
  • Bogotá
  • Buenos Aires
  • Cali
  • Ceará
  • Cercado de Lima
  • Ciudad de Guatemala
  • Ciudad de México
  • Córdoba
  • Floridablanca
  • HPR
  • KZE
  • La Habana
  • Las Condes
  • Montevideo
  • Paraná
  • Rio de Janeiro
  • Rio Grande do Sul
  • Rosario
  • San Isidro
  • San Pedro Garza García
  • Santiago
  • Santo Domingo
  • Surquillo
  • São Paulo
  • Temuco
  • Toluca de Lerdo
Trial Identifier:

NCT04158258 MO39485

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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

      A Prospective, Multicenter, Non-Interventional Study of Primary Data Collection, Designed to Describe the Diagnosis, Anti-Cancer Treatment and Clinical Outcomes in Patients with Breast Cancer in Latin America.

      Hoffmann-La Roche Sponsor
      NCT04158258,MO39485 Trial Identifier
      Bevacizumab, Trastuzumab, Ado-trastuzumab emtamsine, Pertuzumab, Atezolizumab, Capecitabine Treatments
      Breast Cancer Condition
      Official Title

      A STUDY TO OBSERVE PATIENTS CHARACTERISTICS, TREATMENT PATTERNS AND OUTCOMES IN PATIENTS WITH NEWLY DIAGNOSED BREAST CANCER IN LATIN AMERICA

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      Inclusion Criteria
      • Histological confirmed newly diagnosed stage I to IV (recurrent or de novo) breast cancer no more than 12 months prior to site activation, although they can have received anti-cancer treatment during that time
      Exclusion Criteria
      • Patients not receiving treatment for breast cancer with national approved drugs according to standard of care and in line with the current summary of product characteristics (SPC) /local labeling
      • Patients not receiving the Roche studied medicinal product, but a biosimilar

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

       

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