Advanced Ovarian Cancer

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

Advanced Ovarian Cancer

Description

To investigate the efficacy and safety of BIBF 1120 plus chemotherapy as compared to placebo plus chemotherapy in patients with advanced ovarian cancer

Patient Inclusion Criteria:

  • Patients with histologically proven epithelial ovarian cancer, fallopian tube or primary peritoneal cancer of advanced stage, 18 + years of age, life expectancy of at least 6 months

Patient Exclusion Criteria:

  • histologic diagnosis of a benign or borderline tumour or of a malignant tumour of non-epithelial origin of the ovary, the fallopian tube or the peritoneum, clinically relevant non-healing would, ulcer or bone fracture, clinical symptoms of brain metastases

Details
Clinical Study IdentifierTX134751
Last Modified on8 November 2020

Eligibility

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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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