Phase 2 Ovarian Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are a woman aged 18 or older with ovarian, fallopian tube, or primary peritoneal cancer that has come back after previous treatment
- Your cancer has been confirmed by a pathologist as one of these specific types: high grade or low grade papillary serous, high grade or low grade mucinous, clear cell, or high grade endometrioid carcinoma
- You have previously received at least one chemotherapy treatment that included a platinum-based drug, and your cancer stopped responding to platinum-based treatment
- You have not previously received liposomal doxorubicin (a specific chemotherapy drug), and your doctor considers it a suitable treatment option for you
- Your cancer coming back has been confirmed through a biopsy, scan, or a blood test measuring a marker called CA-125
- You are expected to live for more than 6 months
- Your general health and ability to carry out daily activities is at a moderate level or better (confirm with trial site)
- Your heart is functioning at a healthy enough level, as shown by a heart scan (at least 55% ejection fraction)
- Your blood counts, liver, and kidney function are within acceptable ranges based on recent blood tests
- You are not pregnant, not breastfeeding, and are either unable to become pregnant or are willing to use reliable contraception during the study and for 6 months after treatment ends
- You are willing and able to attend all required study visits and live close enough to the trial site to do so
- You have stopped any previous cancer treatments at least 4 weeks before joining the study and have recovered from their side effects
- You may have had surgery to remove tumours, radiation therapy, or previous anthracycline-type chemotherapy drugs and may still be eligible (confirm with trial site)
Who may not be able to join:
- You are in very poor health and have significant limitations in daily activities (confirm with trial site)
- You are pregnant or breastfeeding
- You have received another experimental treatment within the past 4–6 weeks (depending on the type)
- You have cancer that has spread to the brain or the lining of the brain, whether treated or untreated
- You have a known fluid build-up around your heart (pericardial effusion)
- You have an active serious infection or another serious illness, such as heart failure, that could make participation unsafe
- You have had another type of cancer in the past, unless it was a very early-stage cervical condition or a non-melanoma skin cancer, or unless the other cancer was fully treated at least 2 years ago with no signs of return
- You have a condition that causes active or ongoing bleeding
- You are currently receiving other cancer treatments
- You are already taking part in another clinical trial of an experimental treatment
- You have a serious infection, blood poisoning, or active hepatitis
- You have been diagnosed with congestive heart failure, unstable angina, or have had a heart attack in the past 6 months
- You have a known significant disease affecting the lining around your heart
- You are taking medications known to affect your heart's electrical system
- You have a known allergy to the study drug (WFA/ASWD)
- You have previously been treated with liposomal doxorubicin
- You have previously received other anthracycline or anthracenedione type chemotherapy drugs (confirm with trial site, as prior use may affect eligibility depending on dosage)
- Your doctor believes for any other reason that joining the trial would not be safe or appropriate for you
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.
Contact this trial
Principal Investigator: Whitney Goldsberry, MD, Brown Cancer Center at University of Louisville
Phone: (502) 931-1485
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Progression-free survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.