Phase 2 Ovarian Cancer Trial, Recruiting NCT07022535 Sponsor: The University of Hong Kong Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07022535
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 who are at least 18 years old.
  • People who have a good general level of physical functioning, rated 0 or 1 on a standard oncology scale (meaning fully active or able to carry out light activity).
  • People who are able to understand and agree to take part by giving informed consent.
  • People who have been diagnosed with stage III or IV ovarian cancer, fallopian tube cancer, or primary peritoneal cancer — confirmed by tissue or cell testing — where upfront surgery to remove the tumour is not suitable.
  • People who are planned to receive chemotherapy before surgery (called neoadjuvant chemotherapy), using a platinum-based drug, with or without bevacizumab or a similar medicine, including those already planned for surgery after that chemotherapy.
  • People who have a measurable CA125 blood marker level at the start of the trial — specifically, at least twice the upper limit of the normal range.
  • People who have had a CT scan or PET-CT scan of at least the abdomen and pelvis before joining (an MRI scan is also acceptable), and who are able to use the same type of scan later to assess surgical planning.
  • People who agree to undergo surgery to remove as much tumour as possible after chemotherapy, even if the timing may differ from standard practice.
  • People who agree to receive further chemotherapy after surgery if the treating doctor considers it medically appropriate, with a total of at least four chemotherapy cycles overall.

Who may not be able to join:

  • People whose cancer is classified as borderline (low malignant potential), or is a non-epithelial type such as germ cell tumour or sex cord tumour, or has spread from a cancer that started in another organ (such as a Krukenberg tumour).
  • People whose cancer is considered suitable for upfront surgery to remove the tumour directly.
  • People who are not considered suitable for surgery due to other medical conditions, or who do not wish to have surgery.
  • People who have already begun chemotherapy before joining the trial at another centre — except those who have had only one cycle within the past 21 days and whose baseline CA125 result is available.
  • People who are pregnant.

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 15 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: Ka Yu Tse, MBBS, MMedSc, PhD, FRCOG, The University of Hong Kong

Phone: +852 22554265

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
Registry
ClinicalTrials.gov
Start date
28 May 2024
Est. completion
31 December 2025

Where this trial is recruiting

Hong Kong

Primary endpoints

Complete resection (CC0) rate; Sensitivity of KELIM in predicting CC0

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: 15 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