Phase 3 Ovarian Cancer Trial, Recruiting NCT06819007 Sponsor: Daiichi Sankyo Condition: Ovarian Cancer
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Phase 3 Ovarian Cancer Trial, Recruiting

NCT06819007
Recruiting Phase 3 🇦🇺 Australian site

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not 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 may be able to join

  • You must be willing to sign consent forms before any trial-related procedures begin, including consent for optional genetic testing.
  • You must be 18 years of age or older at the time of signing the consent form.
  • You have been diagnosed with a specific type of ovarian, fallopian tube, or primary peritoneal cancer (a high-grade epithelial type, confirmed by tissue testing), including types such as serous, endometrioid, clear cell, carcinosarcoma, or mucinous.
  • You have been newly diagnosed with an advanced stage of the disease (Stage III or IV).
  • Your cancer must show a certain level of a protein called HER2, confirmed through a specific type of tissue test sent to a central laboratory.
  • You must have enough tumor tissue available (a tissue block or slides) for laboratory testing, including HER2 testing and other analysis.
  • You must have an available local test result for HRD (a measure of DNA repair in cancer cells) or BRCA gene status.
  • You have already received up to 6 cycles of standard chemotherapy (platinum-based) combined with a drug called bevacizumab, and your doctor considers you suitable to continue with bevacizumab alone as a maintenance treatment.

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • Your ovarian, fallopian tube, or peritoneal cancer is not of the epithelial type (confirm with trial site).
  • You have a known harmful change in the BRCA gene that would make you eligible for a type of drug called a PARP inhibitor.
  • Your doctor has determined that you should receive a PARP inhibitor as part of your standard maintenance treatment.
  • You have had a serious allergic reaction to any of the drugs used in this trial or to similar types of medications (monoclonal antibodies).
  • You have had a stroke, mini-stroke (TIA), or a type of brain bleed (subarachnoid hemorrhage) within the 6 months before joining the trial.
  • You have a condition where your blood does not clot properly (and you are not on blood-thinning medication).
  • You have a history of abnormal bleeding, an abnormal opening in the bowel or abdomen (fistula or perforation), or active bleeding in the digestive system within the past 6 months.
  • You currently have a blockage in your bowel.
  • You have had a heart attack within the past 6 months, or you have moderate-to-severe heart failure symptoms.
  • Your heart's electrical activity (measured by an ECG test) shows a specific abnormality called a prolonged QT interval above a certain level.
  • You have a history of a lung condition called interstitial lung disease (ILD) or pneumonitis that needed steroid treatment, or you currently have this condition, or it cannot be ruled out based on your scans.

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 24 July 2026

Contact this trial

Phone: 908-992-6400

Australian sites

Genesiscare St Andrews Hospital, Adelaide,
Icon Cancer Centre Wesley, Auchenflower,
Icon Cancer Centre Hobart, Hobart,
Genesis Care North Shore (Oncology), St Leonards,
Westmead Hospital, Sydney,
Townsville University Hospital Cancer Centre, Townsville,

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
Daiichi Sankyo
Registry
ClinicalTrials.gov
Start date
19 March 2025
Est. completion
1 November 2028

Where this trial is recruiting

🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇳 China 🇨🇿 Czechia 🇩🇰 Denmark 🇫🇷 France 🇬🇷 Greece 🇭🇺 Hungary 🇮🇳 India 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇲🇾 Malaysia 🇵🇱 Poland 🇷🇴 Romania 🇸🇬 Singapore 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

6 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Progression Free Survival by Blinded Independent Central Review (BICR) in the HER2 IHC 3+/2+ population

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: 24 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