Back to Ovarian Cancer
NCT00278343
NCT00278343
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer (confirmed by lab testing) that has come back or stopped responding to initial treatment.
- You have previously been treated with a platinum-based chemotherapy drug before joining this trial.
- Your cancer can be measured on a scan, showing at least one visible area of disease, OR your cancer is detectable through a blood test called CA-125 showing elevated levels on two separate tests taken more than 2 weeks apart.
- You have received no more than one prior course of chemotherapy (first-line treatment only).
- Doctors expect you to live for more than 12 weeks.
- You are well enough to carry out basic daily activities (a doctor will assess this using a standard scale).
- Your blood counts, liver function, and kidney function all fall within acceptable levels (confirmed by blood tests).
- If you could become pregnant, you must have a negative pregnancy test before starting the trial and agree to use reliable contraception throughout.
- You are willing and able to understand and sign a consent form agreeing to take part.
Who may not be able to join:
- You have had chemotherapy, radiation therapy, or major surgery within the past 4 weeks (or 6 weeks for certain specific chemotherapy drugs), or you are still experiencing side effects from previous treatment.
- Your tumour has been classified as "borderline" or "low malignant potential" (a less aggressive type of tumour).
- You currently have a bowel blockage (bowel obstruction).
- You are currently taking part in another clinical trial or have done so within the past 30 days.
- Cancer has spread to your brain.
- You have had a serious allergic reaction to a drug that is chemically similar to the trial drug (AZD2171/cediranib maleate).
- A heart tracing test (ECG) shows a specific abnormality in your heart's electrical activity, or you have a family history of a condition called long QT syndrome.
- Urine tests on two separate occasions (at least 1 week apart) show a significant level of protein in your urine.
- You have uncontrolled high blood pressure, an active infection, serious heart problems, or a mental health or personal situation that could make it difficult to follow the trial requirements.
- You are pregnant or currently breastfeeding.
- You are HIV-positive and receiving combination antiretroviral therapy.
- A recent heart tracing test (ECG) taken within the last 14 days shows any significant abnormality.
- You have been assessed as having a severe level of heart failure (classified as Class III or IV by your doctor — Class II patients who are well controlled with treatment may still be considered with extra monitoring).
- You are currently taking certain medications that can affect your heart rhythm, as these cannot be used alongside the trial drug (confirm with trial site).
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.
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Trial details
Status
Completed
Phase
Phase 2
Sponsor
National Cancer Institute (NCI)
Registry
clinicaltrials_gov
Start date
1 April 2006
Est. completion
1 June 2010
Where this trial is recruiting
🇨🇦 Canada
🇺🇸 United States
Primary endpoints
Response Benefit (Complete Response or Partial Response or Stable Disease) Based on the RECIST/Rustin Criteria
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.