NCT00138242

Who might be able to join this trial:

• You have been diagnosed with ovarian, fallopian tube, or peritoneal cavity cancer that has been confirmed by a tissue sample (biopsy), and your cancer is at Stage IC or higher (up to Stage IV)
• You have already had surgery to remove or reduce the cancer, or you are planning to have surgery after starting the study (some patients may receive chemotherapy before surgery first)
• You are 18 years of age or older
• You are reasonably well and able to carry out daily activities (confirm with trial site regarding fitness level assessment)
• Your blood cell counts are at acceptable levels — including white blood cells, red blood cells, and platelets
• Your liver function test results are within acceptable ranges
• You are not pregnant or breastfeeding, and if you could become pregnant, you are willing to use reliable contraception during the trial and for at least 3 months after finishing treatment

Who may not be able to join:

• Your tumor has been classified as "borderline" or "low malignant potential," regardless of stage
• You have significant nerve damage or numbness/tingling in your hands or feet beyond a mild level
• You have a history of another cancer that has a poor outlook and could come back during the trial period (the trial doctors will assess this)
• You have previously had a severe allergic reaction to any medication containing an ingredient called polysorbate 80
• You are currently receiving chemotherapy for a different cancer
• Your liver function test results fall outside the acceptable ranges described for this trial (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.