Clinical Research

ABI/CA0023

Title:

A Randomized Phase II Trial of Weekly vs.. Every Two-Week vs. Every Three-Week Administration of ABI-007 in Combination with Bevacizumab in Women with Metastatic Breast Cancer


Eligibility:

Patients must have pathologically confirmed adenocarcinoma of the breast; Stage IV measurable disease; Must not be a candidate for Herceptin therapy;  Cannot be HER-2 positive or HER-2 unknown; Must be at least four  weeks since radiotherapy with full recovery: The measurable disease must be completely outside the radiation portal or there must be pathologic proof of progression disease within the radiation portal; Patients must be at least four weeks from major surgery with full recover; ECOG performance status 0-2; Female >18 years of age; Meet specific baseline blood chemistry levels (refer to protocol); Negative pregnancy test within 72 hours of first dose (if Applicable); Patients must agree to use an effective method of birth control to avoid pregnancy for the duration of the study; Must have a signed informed consent.

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