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An Observational Study of Avastin (Bevacizumab) in Patients With Metastatic Breast Cancer

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Roche

Status

Completed

Conditions

Breast Cancer

Treatments

Drug: Bevacizumab

Study type

Observational

Funder types

Industry

Identifiers

NCT01215123
ML25100

Details and patient eligibility

About

This observational study will assess the median time of treatment duration and the safety of Avastin (bevacizumab) as first line treatment in patients with metastatic breast cancer. Data will be collected for approximately 24 months.

Enrollment

28 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with metastatic breast cancer in first line treatment who have completed treatment with Avastin

Exclusion criteria

  • Patients not willing or unable to signed written consent form

Trial design

28 participants in 1 patient group

Bevacizumab
Description:
Participants received bevacizumab according to routine clinical practice until disease progression, unacceptable toxicity or withdrawal, along with taxane-based chemotherapy or in combination with other chemotherapy as prescribed.
Treatment:
Drug: Bevacizumab

Trial contacts and locations

12

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Data sourced from clinicaltrials.gov

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