Phase 2 Ovarian Cancer Trial, Recruiting NCT05610735 Sponsor: Sham Sunder Kakar Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT05610735
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
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.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Sham Sunder Kakar
Registry
ClinicalTrials.gov
Start date
25 September 2024
Est. completion
30 November 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression-free survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov