An Interventional Study of Avastin (Bevacizumab) in Patients With Advanced/Metastatic Epithelial Ovarian Cancer, Fallopian Tube Cancer or Primary Peritoneal Cancer

  • End date
    Aug 31, 2023
  • participants needed
  • sponsor
    Hoffmann-La Roche
Updated on 14 June 2022
cancer chemotherapy
ovarian cancer
fallopian tube
ovarian epithelial cancer
peritoneal cancer
primary peritoneal carcinoma
ovarian epithelial carcinoma
cancer of the ovary
epithelial ovarian cancer
stage iv ovarian epithelial cancer


This multicenter prospective study will evaluate the safety and efficacy of Avastin (bevacizumab) in routine clinical practice in patients with advanced/metastatic epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer. Data will be collected from eligible patients until death, withdrawal of consent, loss to follow-up, or study closure.

Condition Ovarian Neoplasms, Peritoneal Neoplasms, Fallopian Tube Neoplasms
Treatment bevacizumab
Clinical Study IdentifierNCT01932125
SponsorHoffmann-La Roche
Last Modified on14 June 2022


Yes No Not Sure

Inclusion Criteria

Prescribed to receive bevacizumab or already ongoing on treatment with bevacizumab for advanced/metastatic ovarian cancer, fallopian tube cancer or primary peritoneal cancer (FIGO Stage IIIb, IIIc and IV) according to routine clinical practice

Exclusion Criteria

Not eligible for treatment with bevacizumab according to the local prescribing information
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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