Available IPD datapackage for study 'A Randomised, Double Blind, Placebo Controlled, Multicentre Study to Evaluate the Efficacy and Safety of Bevacizumab in Combination With Docetaxel in Comparison With Docetaxel Plus Placebo, as First Line Treatment for Patients With HER2 Negative Metastatic and Locally Recurrent Breast Cancer.'

Roche

Description

This study will evaluate the efficacy and safety of 2 doses of Avastin in combination with docetaxel, versus docetaxel plus placebo, in patients with metastatic HER2 negative breast cancer who are candidates for taxane-based chemotherapy but who have not received prior chemotherapy for metastatic disease. The anticipated time on treatment is 1-2 years and the target sample size is 500+ individuals.

Citations (0)

Mentions (0)

Metrics

Dataset Index

0.3

FAIR Score

31%

Citations

0

Mentions

0

Metrics Over Time

Publication Details

DOI

Publisher

Vivli

License

Study data may be accessed by completing a request form at https://vivli.org. It will then be reviewed according to the data contributor’s governance policy, see https://vivli.org/members/ourmembers/ for Vivli member’s review process. If approved, use of the data is governed by the data use agreement at https://vivli.org/resources/vivli-data-use-agreement/

Assigned Domain

Subfield

Cancer Research

Field

Biochemistry, Genetics and Molecular Biology

Domain

Life Sciences

Confidence Score

58%

Source

Scholar Data Model

Keywords

Conditions: Breast CancerInterventions: DocetaxelInterventions: Placebo to bevacizumabInterventions: Bevacizumab

Normalization Factors

FT

40.38

CTw

1.00

MTw

1.00