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Spots Global Cancer Trial Database for OGX-011 and Docetaxel in Treating Women With Locally Advanced or Metastatic Breast Cancer

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Trial Identification

Brief Title: OGX-011 and Docetaxel in Treating Women With Locally Advanced or Metastatic Breast Cancer

Official Title: A Phase II Study of a Second Generation Clusterin Antisense Oligonucleotide (OGX-011) in Combination With Docetaxel in Advanced Breast Cancer

Study ID: NCT00258375

Conditions

Breast Cancer

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. OGX-011 may help docetaxel kill more tumor cells by making tumor cells more sensitive to the drug. PURPOSE: This phase II trial is studying how well giving OGX-011 together with docetaxel works in treating women with locally advanced or metastatic breast cancer.

Detailed Description: OBJECTIVES: Primary * Determine the efficacy of OGX-011 and docetaxel, in terms of objective tumor response rate, in women with locally advanced or metastatic breast cancer. Secondary * Determine the tolerability and toxicity of this regimen in these patients. * Determine the time to progression and overall survival of patients treated with this regimen. OUTLINE: This is an open-label, nonrandomized, multicenter study. Patients receive OGX-011 IV over 2 hours on days -7, -5, -3, 1, 8, and 15 of course 1 and on days 1, 8, and 15 of all subsequent courses. Patients also receive docetaxel IV over 1 hour on days 1 and 8 of all courses. Treatment repeats every 21 days\* for up to 10 courses in the absence of disease progression or unacceptable toxicity. NOTE: \*Course 1 is 28 days in length and all subsequent courses (courses 2-10) are 21 days in length. After completion of study treatment, patients are followed at 4 weeks and then periodically until disease progression. PROJECTED ACCRUAL: Approximately 42 patients will be accrued for this study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

British Columbia Cancer Agency - Centre for the Southern Interior, Kelowna, British Columbia, Canada

BCCA - Fraser Valley Cancer Centre, Surrey, British Columbia, Canada

British Columbia Cancer Agency - Vancouver Cancer Centre, Vancouver, British Columbia, Canada

London Regional Cancer Program at London Health Sciences Centre, London, Ontario, Canada

Ottawa Hospital Regional Cancer Centre - General Campus, Ottawa, Ontario, Canada

Contact Details

Name: Stephen Chia, MD

Affiliation: British Columbia Cancer Agency

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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