NCT00390234
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with a soft tissue sarcoma (a type of cancer) of the female reproductive system, specifically uterine leiomyosarcoma, malignant mixed mullerian tumor/carcinosarcoma, or a similar cancer starting in the ovary or fallopian tube (confirmed by lab testing)
- Your cancer cannot be fully removed by surgery, has spread to other parts of the body, or is locally advanced
- If you have been treated before, there must be clear evidence (from scans or clinical assessment) that your cancer has continued to grow or spread
- Your cancer can be measured on a scan — at least one tumor measuring 20mm or larger using standard imaging, or 10mm or larger using a spiral CT scan
- The tumor being measured has not been previously treated with surgery, radiation, or similar procedures — unless it has since grown or spread
- You are reasonably active and able to care for yourself (confirm with trial site for specific activity level requirements)
- Your doctors estimate you have a life expectancy of at least 3 months
- Your blood counts are within acceptable ranges — including white blood cells, infection-fighting cells (neutrophils), and platelets (confirm with trial site for exact values)
- Your liver function, kidney function, and blood clotting results are within acceptable ranges (confirm with trial site for exact values)
- There is only a small amount (or no) protein found in your urine
- You are not pregnant or breastfeeding, and have taken a pregnancy test with a negative result
- If you are able to become pregnant, you are willing to use effective birth control during the trial and for at least 6 months after treatment ends
- You have had no more than 2 previous chemotherapy treatments for your advanced or returning cancer
- You have recovered from any side effects of previous treatments
- You have not previously been treated with a medication that targets blood vessel growth (antiangiogenic therapy)
- You have not had another active cancer in the past 5 years, except for certain early-stage skin cancers or cervical carcinoma in situ that were fully treated
Who may not be able to join:
- It has been less than 4 weeks since your last chemotherapy, experimental treatment, radiation, or major surgery (or less than 6 weeks for certain specific chemotherapy drugs)
- It has been less than 1 week since a tissue biopsy using a needle
- It has been less than 1 month since you used a clot-dissolving medication
- You have signs of cancer that has spread to the brain, or you have a primary brain tumor
- You have a known serious allergy to certain types of laboratory-made proteins or antibodies used to make the study drugs (confirm with trial site)
- You have a known allergy to substances chemically similar to the study drugs
- You have a wound, ulcer, or bone fracture that has not healed properly
- You have had a hole or tear in the intestines, a bowel blockage, an internal abdominal infection, or an abnormal connection in the abdomen in the past 28 days
- You have had a significant injury or trauma in the past 28 days
- You have a condition that causes problems with blood clotting or unusual bleeding
- You have an ongoing or uncontrolled infection, or mental health or personal circumstances that would make it difficult to follow the trial requirements
- You have serious or uncontrolled heart or blood vessel problems, including a stroke in the past 6 months, a heart attack or heart surgery in the past 6 months, serious heart failure or irregular heartbeat, uncontrolled high blood pressure, or significant circulation problems in the past 6 months
- You have had a blood clot (such as a pulmonary embolism or deep vein thrombosis) in the past 6 months
- You are HIV-positive and taking combination antiretroviral therapy
- You are currently taking part in another clinical trial or receiving another experimental treatment
- You are scheduled for or currently undergoing major surgery at the same time as this trial
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Trial details
Where this trial is recruiting
Primary endpoints
Objective Response Rate, Evaluated According to the RECIST Criteria; Incidence of Disease Stabilization, as Measured by Progression-free Survival at 6 Months (Leiomyosaroma Group); Incidence of Disease Stabilization, as Measured by Progression-free Survival at 6 Months (Carcinosarcoma Group)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.