Ovarian Cancer Trial, Recruiting NCT06836219 Sponsor: Consorzio Oncotech Condition: Ovarian Cancer
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Ovarian Cancer Trial, Recruiting

NCT06836219
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 at the time of their cancer diagnosis
  • People diagnosed with a specific type of ovarian, fallopian tube, or peritoneal cancer (high-grade serous or endometrioid) who had a validated genetic tumour test (such as MyChoice HRD, FoundationOne DX, or a similar approved test) performed between January 2021 and January 2026
  • People whose tumour test showed a high HRD score (above 42) or high LOH result, indicating a DNA repair deficiency, and who were treated with Bevacizumab and Olaparib after first-line platinum-based chemotherapy — these people may be enrolled in Cohort A
  • People whose tumour test showed a low HRD score (below 42) or low LOH result, indicating normal DNA repair, and who were treated with first-line platinum-based chemotherapy with or without Bevacizumab or other targeted medicines — these people may be enrolled in Cohort B
  • People who are able to understand the study procedures and are willing to provide written consent to participate

Who may not be able to join:

  • People who have not had a validated genetic DNA repair test performed on a tumour sample
  • People who have a BRCA1 or BRCA2 gene mutation (either inherited or developed in the tumour)
  • People who have passed away at the time of enrolment into the study

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 9 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

Phone: +39 334 500 7736

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
Not Applicable
Sponsor
Consorzio Oncotech
Registry
ClinicalTrials.gov
Start date
13 September 2024
Est. completion
1 January 2029

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Evaluate the clinical outcomes; Evaluate the clinical outcomes; Evaluate the safety in patients treated with targeted anticancer therapies in each study cohort; Evaluate the safety in patients treated with targeted anticancer therapies in each study cohort; Evaluate the safety in patients treated with targeted anticancer therapies in each study cohort; Evaluate the safety in patients treated with targeted anticancer therapies in each study cohort; Evaluate the safety in patients treated with targeted anticancer therapies in each study cohort; Evaluate the safety in patients treated with target...

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: 9 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