TrialSignal
Clinical trial intelligence report
An Open-label Study to Evaluate the Safety and Effect on Disease Progression and Overall Survival of Avastin Plus Taxane-based Chemotherapy in Patients With Locally Recurrent or Metastatic Breast Cancer
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00448591-Jul 28, 2026
NCT ID
NCT00448591
Status
COMPLETED
Phase
Phase 3
Sponsor
Hoffmann-La Roche
Executive brief
Investment-Ready Snapshot
The study evaluates the combination of Avastin and taxane-based chemotherapy in patients with locally recurrent or metastatic HER-2 negative breast cancer. Given the substantial patient population (500+), the results could reinforce Avastin's positioning in the competitive landscape against other therapies targeting similar indications. The market for breast cancer treatments remains robust, with ongoing demand for effective first-line therapies. Competitive analysis suggests that while Avastin faces competition from other anti-VEGF agents and novel therapies, its established use and safety profile may provide a strategic advantage. Diligence should focus on the long-term efficacy and safety data, as well as potential regulatory hurdles in various markets.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00448591
Indication
Breast Cancer
Modality
small molecule
Target
VEGF (Vascular Endothelial Growth Factor) inhibition via Bevacizumab (Avastin)
Intervention
bevacizumab [Avastin], Taxane-based chemotherapy
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.