Phase 3 Ovarian Cancer Trial, Recruiting NCT06476184 Sponsor: ARCAGY/ GINECO GROUP Condition: Ovarian Cancer
Back to Ovarian Cancer

Phase 3 Ovarian Cancer Trial, Recruiting

NCT06476184
Recruiting Phase 3

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 been diagnosed with a specific type of ovarian, peritoneal, or fallopian tube cancer — confirmed by laboratory testing — including high-grade serous, endometrioid, or carcinosarcoma (with at least 30% epithelial tumour component) types.
  • People who are 18 years of age or older.
  • People whose cancer is at an advanced stage (Stage III or IV).
  • People who have already received 3 to 4 rounds of standard pre-surgery chemotherapy (carboplatin and paclitaxel, given every 3 weeks), whose CA-125 blood marker results showed a poor response to that chemotherapy (a KELIM score below 1.0), and whose cancer was not able to be fully removed by surgery.
  • People with a good general level of physical functioning — rated 0 or 1 on a standard medical scale, meaning fully active or able to carry out light activity (confirm with trial site).
  • People whose blood counts are at acceptable levels, including haemoglobin, white blood cells, and platelets, without having needed a blood transfusion in the 3 weeks before testing.
  • People whose kidneys and liver are functioning at adequate levels, as measured by specific blood tests (confirm specific values with trial site).
  • People who are willing and able to attend all required treatment sessions, appointments, and follow-up visits for the full duration of the trial.
  • People who have signed a written consent form agreeing to take part in the study.
  • People who are covered by a social insurance or healthcare scheme.

Who may not be able to join:

  • People whose cancer is a low-grade, clear cell, mucinous, or certain other specific tumour types, or those who have a known allergy or medical reason preventing the use of carboplatin, paclitaxel, or GCSF (a drug used to support white blood cell levels).
  • People who received bevacizumab (a targeted therapy) as part of their initial pre-surgery chemotherapy.
  • People whose cancer continued to grow or spread during their pre-surgery chemotherapy, indicating it did not respond to platinum-based treatment.
  • People who currently have another active cancer, unless it is a previously treated, non-melanoma skin cancer, fully treated cervical cancer in situ, or another cancer that was fully treated with no signs of return for 5 or more years.
  • People who are currently taking part in another clinical trial involving an experimental treatment.
  • People with serious uncontrolled health conditions, which may include unstable heart problems, a heart attack within the past 6 months, severe uncontrolled high blood pressure, serious heart rhythm problems, heart failure, liver cirrhosis, an active serious infection requiring intravenous antibiotics within the past 2 weeks, or certain bowel blockage or obstruction issues (confirm specific details with trial site).
  • People with a known psychiatric condition that the trial team believes would affect their ability to follow the trial requirements.
  • People who are pregnant, currently breastfeeding, or planning to have children during the period covered by the trial.
  • People who are legally under guardianship, curatorship, or who are not free to make their own decisions (confirm with trial site).

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 3: approximately ~65% 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: Benoit YOU, HCL - Centre Hospitalier Lyon Sud

Phone: +33 1 84 85 20 20

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 3
Sponsor
ARCAGY/ GINECO GROUP
Registry
ClinicalTrials.gov
Start date
30 July 2024
Est. completion
1 June 2027

Where this trial is recruiting

🇫🇷 France 🇮🇹 Italy 🇯🇵 Japan

Primary endpoints

Percentage of patients operated with late complete debulking surgery; Overall survival (OS)

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