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Observational Studies of the Application of Bevacizumab in HER2-negative Breast Cancer Neoadjuvant Chemotherapy

Observational Studies of the Application of Bevacizumab in HER2-negative Breast Cancer Neoadjuvant Chemotherapy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01652560
Acronym
BIBC
Enrollment
50
Registered
2012-07-30
Start date
2012-06-30
Completion date
2014-09-30
Last updated
2012-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bevacizumab, Breast Cancer, Molecular Targeted Therapy, Neoadjuvant Chemotherapy

Keywords

bevacizumab, neoadjuvant chemotherapy, HER2-negative breast cancer

Brief summary

\- The purpose of this study is to evaluate the efficacy and safety of the application of bevacizumab combined neoadjuvant chemotherapy in HER2-negative breast cancer.

Interventions

DRUGbevacizumab

The patients will be treated with Avastin combined neoadjuvant chemotherapy

Sponsors

Roche Pharma AG
CollaboratorINDUSTRY
LiNanlin,Ph.D, Chief Physician,Clinical Professor
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* HER2-negative breast cancer patients * Without surgery * Plans to neoadjuvant chemotherapy

Exclusion criteria

* HER2-positive breast cancer patients * Post-operative patients

Design outcomes

Primary

MeasureTime frameDescription
Objective Response RateFrom enrollment to disease progressionFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 5 years.

Secondary

MeasureTime frameDescription
overall responseFrom enrollment to disease progressionFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 5 years.

Countries

China

Contacts

Primary ContactNanlin Li, Phd
nanlin-74@163.com+86-186-2963-7041
Backup ContactHongyu Xiao, Master
louch2008@116.com+86-186-2963-7040

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026