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NCT03804866
NCT03804866
Who may be able to join
Who might be able to join this trial:
- You are 18 years of age or older
- You have been diagnosed (confirmed by a tissue sample/biopsy) with advanced or metastatic ovarian cancer, fallopian tube cancer, or primary peritoneal cancer
- You have received no more than two previous chemotherapy treatments that included a platinum-based drug plus paclitaxel, and your cancer either did not respond to treatment or came back within 6 months of your last chemotherapy
- You are reasonably active and able to care for yourself, with only limited restrictions on daily activity (confirm with trial site)
- Doctors expect you to live for at least 12 weeks or more
- Your heart is functioning normally and your blood pressure is under control
- Your blood counts, liver, and kidney function are within acceptable levels as measured by blood tests (confirm with trial site)
- You have at least one area of cancer that can be tracked or measured and has not previously been treated with radiation
- If you have had surgery, radiation, or other cancer treatments, enough time has passed since your last treatment (at least 14 days after surgery/radiation, or 21 days after other cancer treatments)
- You are willing and able to sign a consent form agreeing to take part in the study
Who may not be able to join:
- You are currently taking part in another clinical trial involving an experimental treatment
- You have had more than two previous chemotherapy treatments, or you have previously been treated with a type of chemotherapy called an anthracycline
- You have had a heart attack in the last six months, have unstable chest pain (angina), moderate-to-severe heart failure, or a serious irregular heartbeat that requires medication
- You have an abnormal heart rhythm measurement on an ECG (a reading called QTc interval greater than 450 ms), whether inherited or developed
- You have a history of, or signs of, a condition affecting your brain or nervous system that has not been adequately treated (confirm with trial site)
- You have an active or poorly controlled serious infection or other serious health condition that would make participating unsafe
- You have a known allergy or sensitivity to human albumin or any of the ingredients used in the study drug
- There are personal, family, social, or location-related reasons that might make it difficult for you to follow the study requirements
- You are currently pregnant or breastfeeding
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
AGC Biologics S.p.A.
Registry
clinicaltrials_gov
Start date
1 March 2013
Est. completion
1 December 2016
Where this trial is recruiting
🇮🇹 Italy
Primary endpoints
Safety according to NCI-CTCAE criteria (version 4.03)
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.