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NCT01204749
NCT01204749
Who may be able to join
Who might be able to join this trial:
- You are a woman aged 18 or older at the time you sign the consent form
- You are in good enough general health to carry out light activity and care for yourself (your doctor will assess this)
- Your doctor expects you to live for at least 3 months or longer
- You have been diagnosed with invasive epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer, confirmed by a tissue or cell sample
- You have had surgery for your cancer that included removal of at least one ovary
- Your cancer can be seen and measured on a scan
- You have received one prior chemotherapy treatment containing a platinum-based drug (such as carboplatin or cisplatin) for your cancer
- Your kidneys, liver, blood, and other organs are functioning well enough to participate
- Your blood pressure is generally well controlled, with readings at or below 140/90 mmHg (blood pressure medication to help control this is allowed)
- Your scans show that your cancer has grown or spread either during or after your most recent chemotherapy treatment
Who may not be able to join:
- You have received more than 3 separate anti-cancer treatments for your ovarian, peritoneal, or fallopian tube cancer
- You have previously received paclitaxel on its own or as a maintenance or consolidation treatment
- Your cancer did not respond to platinum-based chemotherapy from the very beginning (primary platinum-refractory disease — confirm with trial site)
- It has been more than 12 months since your last platinum-based chemotherapy
- You have had radiotherapy within the last 14 days before joining the trial, or you have not fully recovered from its side effects
- You have previously had radiotherapy to your abdomen or pelvis at any time
- You have had a blood clot in an artery or vein within the past 12 months
- You have had a significant bleeding episode within the past 6 months
- Your cancer has spread to your brain or central nervous system
- You have not waited at least 21 days after finishing your last cancer treatment before joining (or 30 days if that treatment included bevacizumab)
- You are currently in another clinical trial or have not waited at least 30 days since finishing one
- You still have significant side effects (grade 2 or higher) from previous cancer treatments, apart from hair loss
- You have had an active infection (other than a simple urinary tract infection) within the last 14 days
- You have previously been treated with AMG 386 or similar drugs that target the same biological pathway (angiopoietins or Tie2 receptor — confirm with trial site)
- You have taken strong immune-suppressing medications (such as cyclosporine, methotrexate, thalidomide, or similar drugs) within the last 30 days
- You have had a significant heart or blood vessel problem within the past 12 months
- You have had major surgery within the last 28 days, or you are still recovering from surgery
- You have had a minor surgical procedure (other than insertion of a central line or a diagnostic laparoscopy) within the last 3 days
- Your cancer type is pseudomyxoma, mesothelioma, sarcoma, neuroendocrine, unknown primary, borderline (low malignant potential), clear cell, or mucinous (these specific cancer types are not eligible)
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
Completed
Phase
Phase 3
Sponsor
Amgen
Registry
clinicaltrials_gov
Start date
1 November 2010
Est. completion
1 March 2013
Where this trial is recruiting
🇦🇺 Australia
🇧🇪 Belgium
🇧🇷 Brazil
🇧🇬 Bulgaria
🇨🇦 Canada
🇨🇱 Chile
🇭🇷 Croatia
🇨🇿 Czechia
🇪🇪 Estonia
🇫🇷 France
🇬🇷 Greece
Hong Kong
🇮🇳 India
🇮🇱 Israel
🇮🇹 Italy
🇯🇵 Japan
🇱🇻 Latvia
🇲🇾 Malaysia
🇲🇽 Mexico
🇵🇪 Peru
🇵🇱 Poland
🇵🇹 Portugal
🇷🇴 Romania
🇷🇺 Russia
🇸🇮 Slovenia
🇿🇦 South Africa
🇰🇷 South Korea
🇪🇸 Spain
🇸🇪 Sweden
🇨🇭 Switzerland
🇬🇧 United Kingdom
🇺🇸 United States
7 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Progression-Free Survival
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.