Back to Ovarian Cancer
NCT00086892
NCT00086892
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with ovarian cancer or primary peritoneal cancer (confirmed by a lab test on tissue samples) that has come back after previous treatment
- Your cancer can be measured on a scan or by physical examination (there is at least one tumor large enough to be tracked)
- The tumor being measured is not in an area that was previously treated with radiation
- You previously received one round of chemotherapy containing a platinum-based drug (such as carboplatin or cisplatin) as your main treatment
- Your cancer responded to that platinum-based chemotherapy, and you had more than 6 months without signs of the cancer coming back before it returned
- In some cases, a treatment-free period of more than 12 months may be required depending on other available trials (confirm with trial site)
- A tissue sample from your tumor (either a tissue block or slides) is available for research
- You are 18 years of age or older
- You are well enough to carry out everyday activities with little or no limitation (confirm with trial site)
- Your blood counts are at acceptable levels — enough white blood cells and platelets
- Your liver and kidney function are within acceptable ranges based on blood tests
- You have had a negative pregnancy test (if applicable)
- If you are able to become pregnant, you are willing to use effective birth control during the trial
Who may not be able to join:
- Your cancer has not come back — this trial is only for recurrent disease
- You have already received chemotherapy specifically to treat the cancer after it came back
- You have no measurable tumor that can be tracked on a scan or by examination
- You have uncontrolled high blood pressure
- You have unstable chest pain (angina), heart failure, or an uncontrolled irregular heartbeat within the past 6 months
- You have another significant heart condition
- You have an uncontrolled seizure disorder or an active neurological (brain or nerve) disease
- You have significant nerve damage or numbness/tingling beyond a mild level
- You have had another serious cancer (other than certain common skin cancers) within the past 5 years
- You have an active infection that requires antibiotic treatment
- You are pregnant or breastfeeding
- You have previously been treated with certain targeted therapies that affect a protein called EGFR (epidermal growth factor receptor), including specific antibody treatments or tyrosine kinase inhibitor drugs
- You have previously received a type of antibody therapy called a chimerized or murine monoclonal antibody
- You have received radiation to more than 25% of the areas of your body where bone marrow is produced
- You have had major surgery within the past 30 days and have not yet fully recovered
- You are currently taking part in another experimental treatment study
- You may be eligible for a higher-priority trial within the same research group (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
Gynecologic Oncology Group
Registry
clinicaltrials_gov
Start date
1 June 2004
Est. completion
1 April 2006
Where this trial is recruiting
🇦🇺 Australia
🇨🇦 Canada
🇯🇵 Japan
🇳🇴 Norway
🇺🇸 United States
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
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.