Back to Ovarian Cancer
NCT00849667
NCT00849667
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with a specific type of ovarian cancer (non-mucinous epithelial ovarian cancer), or a related cancer starting in the peritoneum or fallopian tubes, confirmed by a lab test
- Your cancer can be measured on a CT or MRI scan
- Your cancer has come back between 6 and 24 months after finishing your first course of platinum-based chemotherapy
- You have previously had surgery to remove as much of the tumour as possible, followed by chemotherapy using platinum and taxane drugs
- You may have previously received bevacizumab as a maintenance treatment, as long as your last dose was at least 30 days before the study starts (no other maintenance chemotherapy or cancer vaccine treatments are allowed)
- You are considered suitable to receive carboplatin and taxane chemotherapy again
- You have little or no nerve damage (such as numbness or weakness) from previous treatment (confirm with trial site)
Who may not be able to join:
- Your cancer did not respond to your first platinum-based chemotherapy, or it came back either less than 6 months or more than 24 months after finishing it
- You have already received any treatment for your cancer since it came back
- The cancer has spread to your brain or central nervous system
- You have had another active serious cancer that required treatment within the last 5 years
- You have had a known allergic reaction to a monoclonal antibody treatment before, or have developed certain antibodies against such treatments (confirm with trial site)
- You have previously been treated with a drug called MORAb-003 (farletuzumab)
- There is a medical reason why you cannot safely receive taxane chemotherapy
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 3: approximately ~65% 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
Terminated
Phase
Phase 3
Sponsor
Morphotek
Registry
clinicaltrials_gov
Start date
16 April 2009
Est. completion
31 December 2012
Where this trial is recruiting
🇦🇷 Argentina
🇦🇺 Australia
🇦🇹 Austria
🇧🇪 Belgium
🇧🇷 Brazil
🇨🇦 Canada
🇨🇱 Chile
🇫🇷 France
🇩🇪 Germany
🇬🇷 Greece
Hong Kong
🇭🇺 Hungary
🇮🇳 India
🇮🇱 Israel
🇮🇹 Italy
🇯🇵 Japan
🇲🇽 Mexico
🇳🇱 Netherlands
🇵🇭 Philippines
🇵🇱 Poland
🇵🇹 Portugal
🇷🇺 Russia
🇸🇬 Singapore
🇰🇷 South Korea
🇪🇸 Spain
🇨🇭 Switzerland
🇹🇼 Taiwan
🇺🇦 Ukraine
🇬🇧 United Kingdom
🇺🇸 United States
6 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Progression-free Survival (PFS)
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.