Phase 2 Ovarian Cancer Trial, Recruiting NCT07460180 Sponsor: The Netherlands Cancer Institute Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07460180
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 have signed a written consent form agreeing to take part in the study
  • People who are at least 18 years old and able to understand the patient information provided
  • People diagnosed with stage III high-grade serous ovarian cancer, fallopian tube cancer, or related cancer originating outside the ovary (based on the FIGO staging system)
  • People with stage IV cancer may also be considered in specific situations, such as when the cancer has spread to a limited area of the bowel, the abdominal wall, or the belly button area and can be surgically removed, or when stage IV is based only on small lymph nodes near the heart and diaphragm that are less than 1cm in size
  • People whose diagnosis has been confirmed through tissue sampling (biopsy) or fluid testing (cytology), with additional laboratory tests used to confirm the diagnosis if only fluid testing was used
  • People who are planned for a specific type of surgery called interval cytoreductive surgery with HIPEC (a procedure that removes tumours and uses heated chemotherapy inside the abdomen), after receiving at least 3 rounds of a standard chemotherapy combination
  • People whose cancer has not grown or spread during chemotherapy — it must be stable or have responded to treatment
  • People whose suitability for surgery has been reviewed by a team of specialists using scans or a keyhole examination of the abdomen, and where complete or near-complete tumour removal is considered achievable
  • People who are physically well enough for major surgery, with a general health score of 0–2 on the WHO scale (ranging from fully active to capable of some self-care)
  • People with adequate bone marrow function, as shown by blood test results meeting specific minimum levels for red blood cells, white blood cells, and platelets (confirm with trial site for exact values)
  • People with adequate liver function, based on blood tests showing liver enzyme and bilirubin levels within an acceptable range
  • People with adequate kidney function, based on a kidney filtration measurement meeting a minimum threshold (confirm with trial site for exact method used)

Who may not be able to join:

  • People who have previously been treated with chemotherapy for a different cancer
  • People who wish to preserve their fertility and are seeking fertility-sparing surgery
  • People who are currently taking certain strong medications that significantly affect how the body processes a specific group of drugs (called CYP3A4 inducers or inhibitors, as assessed using a Dutch medication reference tool), and where those medications cannot be temporarily stopped

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: 0205129111

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
The Netherlands Cancer Institute
Registry
ClinicalTrials.gov
Start date
1 May 2025
Est. completion
1 May 2027

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Safety and toxicity of combining PARP-inhibitors with HIPEC

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