Phase 2 Ovarian Cancer Trial, Recruiting NCT04518501 Sponsor: Xing Xie Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT04518501
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:

  • People aged 18 to 70 years old
  • People diagnosed with high-grade epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer (specifically serous or endometrioid types)
  • People who have received at least two rounds of platinum-based chemotherapy, where the cancer came back within six months of the last treatment, or where the cancer did not respond to platinum-based chemotherapy during at least two cycles
  • People whose cancer can be measured on scans according to standard criteria (RECIST 1.1)
  • People with a general health status rated 0 to 2 on a standard scale (meaning able to carry out daily activities with little to moderate limitation)
  • People with a life expectancy of at least 12 weeks
  • People who have had their BRCA1/2 gene mutation status confirmed through testing
  • People who have never previously been treated with PARP inhibitor medications
  • People whose heart is pumping at 50% or above on assessment
  • People whose bone marrow, blood counts, liver, and kidney function meet specific minimum levels on lab tests (confirm exact values with trial site)
  • People of childbearing age who agree to use effective contraception during the trial, have a negative pregnancy test, and are not breastfeeding
  • People who have signed the trial's informed consent form

Who may not be able to join:

  • People who have previously received PARP inhibitor treatment, unless they stopped due to cost or adherence reasons without the disease progressing, or unless they received only one prior PARP inhibitor (not fuzuloparib) as maintenance therapy for 12 months or more — and in either case, the last PARP inhibitor treatment must have been more than 6 months before joining the trial (confirm with trial site)
  • People who have received radiotherapy to more than 20% of their bone marrow within the past week
  • People who have had another cancer diagnosed in the past 5 years, except for fully treated cervical carcinoma in situ or certain non-melanoma skin cancers
  • People with a serious ongoing infection that requires active treatment
  • People with a known allergy or intolerance to fuzuloparib, arsenic trioxide, or the inactive ingredients in these medications
  • People with moderate or severe peripheral neuropathy (nerve damage causing numbness or pain, rated grade 2 or higher on a standard scale)
  • People whom the trial researchers consider unsuitable for participation for other reasons

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

Phone: 13588193832

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
Xing Xie
Registry
ClinicalTrials.gov
Start date
1 July 2020
Est. completion
3 December 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

ORR

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