Ovarian Cancer Trial, Recruiting NCT06844136 Sponsor: Pierian Biosciences Condition: Ovarian Cancer
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Ovarian Cancer Trial, Recruiting

NCT06844136
Recruiting Not Applicable

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:

  • Women aged 18 or older
  • People who have been diagnosed (confirmed by laboratory analysis of tissue) with either advanced-stage epithelial ovarian cancer, advanced-stage primary peritoneal carcinomatosis (a cancer affecting the lining of the abdomen), or advanced-stage fallopian tube carcinoma — whether newly diagnosed or returned after previous treatment
  • People who had a tissue or fluid sample taken from the tumour or abdominal area before starting chemotherapy, which was used for a specific laboratory test called the ChemoINTEL assay
  • People who have received at least 3 cycles of standard chemotherapy for their condition, using one or more of the following drugs: Carboplatin, Cisplatin, Cyclophosphamide, Docetaxel, Doxorubicin, Etoposide, Fluorouracil, Gemcitabine, Ifosfamide, Irinotecan, Oxaliplatin, Paclitaxel, Pemetrexed, Topotecan, Vinorelbine, or Bevacizumab (Avastin)
  • People who have had their response to treatment assessed after their third and sixth chemotherapy cycles, using standard measurement methods
  • People who have signed a consent form agreeing to take part in the trial

Who may not be able to join:

  • People who have not signed the required consent form to participate
  • People whose cancer is a type other than advanced-stage epithelial ovarian cancer, primary peritoneal carcinomatosis, or fallopian tube carcinoma
  • People who did not receive standard chemotherapy from the list of drugs specified above
  • People whose tissue or fluid sample did not contain enough living cells to complete the minimum required ChemoINTEL laboratory testing for Carboplatin, Cisplatin, Docetaxel, and Paclitaxel

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 13 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Robert Henry, Pierian Biosciences Ltd

Phone: +44 (0)333 034 1690

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
Not Applicable
Sponsor
Pierian Biosciences
Registry
ClinicalTrials.gov
Start date
22 November 2023
Est. completion
31 July 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Prediction Algorithm

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: 13 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