Phase 2 Ovarian Cancer Trial, Recruiting NCT06504147 Sponsor: Oncoinvent Solutions AS Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06504147
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 willing and able to give written consent and follow the study's rules and schedule
  • You are a woman aged 18 or older
  • You have been diagnosed with a specific type of advanced ovarian, fallopian tube, or peritoneal cancer (high-grade serous or high-grade endometrioid, at an advanced stage known as FIGO Stage IIIB/C or IV)
  • Your cancer spread (including in the abdomen) is considered removable by surgery with no tumour left behind
  • Any side effects from previous cancer treatment have mostly cleared up (hair loss is an exception)
  • Your tumour has been tested and confirmed to be "HR proficient" (a specific tumour characteristic — confirm with trial site)
  • You have received chemotherapy before surgery (NACT), and your cancer has stayed stable or shrunk, and doctors think you are suitable for surgery
  • You are well enough to have the surgery and follow-on treatment, based on a standard fitness scale (ECOG score of 0–2)
  • Your kidneys are working well enough, based on a blood/urine test result
  • Your liver is working well enough, based on blood test results
  • Your blood counts (white blood cells, platelets, and haemoglobin) meet minimum levels shown in blood tests
  • If you could become pregnant, you have a negative pregnancy test before joining the trial
  • If you could become pregnant, you agree to use a highly effective form of contraception during treatment and for at least 9 months afterwards (specific methods are listed — confirm with trial site)

Who may not be able to join:

  • You have a known BRCA1 or BRCA2 gene mutation, or your tumour is confirmed to be "HR deficient" (confirm with trial site)
  • There is concern that the study drug may not stay where it should in your body after being given (confirm with trial site)
  • Your cancer is a specific type not covered by this trial, such as borderline tumours, clear cell, mucinous, or certain other rare types, or your cancer has come back after previous treatment
  • You have cancer that has spread to the brain and is causing symptoms
  • You have had another cancer in the past 3 years (some exceptions apply, such as certain early-stage skin or cervical cancers — confirm with trial site)
  • You have previously had radiotherapy to your abdomen or pelvis
  • Your cancer got worse during the chemotherapy given before surgery
  • You are pregnant or breastfeeding
  • You have an active infection currently being treated with antibiotics or causing recurring fevers
  • You have active hepatitis B, hepatitis C, or HIV
  • You have heart failure or a significant heart condition (NYHA Class III or IV)
  • You have any other health condition that the doctors feel could put you at risk or affect the study results
  • In the doctor's opinion, you are unable to follow the study procedures or give proper informed consent
  • You have taken part in another drug trial within the past 4 weeks (or within a specific time window based on that drug — confirm with trial site)
  • You have received other cancer treatments within 4 weeks before or after the planned surgery
  • You have been treated with a drug called bevacizumab within 5 weeks before surgery
  • You have a known allergy to any ingredient in the study drug

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 27 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: 004722183305

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
Oncoinvent Solutions AS
Registry
ClinicalTrials.gov
Start date
15 June 2024
Est. completion
29 February 2028

Where this trial is recruiting

🇧🇪 Belgium 🇮🇹 Italy 🇳🇴 Norway 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Progression free survival

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: 27 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