Phase 2 Ovarian Cancer Trial, Recruiting NCT06819215 Sponsor: Zhejiang Yangli Pharmaceutical Technology Co., Ltd. Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06819215
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 must be 18 years old or older at the time of screening.
  • Your cancer must have been confirmed by a tissue or cell sample test (such as a biopsy).
  • Your cancer must be at an advanced stage and still growing or spreading at the time you enter the study.
  • Your blood, liver, kidneys, and other organs must be functioning well enough to meet the study's requirements (confirm with trial site for specific details).
  • You must have a specific change (mutation) in certain genes related to DNA repair, known as homologous recombination repair genes (confirm with trial site for specific testing requirements).

Who may not be able to join:

  • You may not be eligible if you have had major surgery within the 4 weeks before starting the trial treatment.
  • You may not be eligible if you have cancer that has spread to the spinal cord or brain, unless it has been treated, is stable, causing no symptoms, and you have not needed more than a low dose of steroid medication for at least 4 weeks before the trial starts.
  • You are not eligible if cancer has spread to the membranes surrounding the brain and spinal cord (a condition called leptomeningeal carcinomatosis).
  • You are not eligible if you have, or show signs of having, certain blood or bone marrow conditions called myelodysplastic syndrome (MDS) or acute myeloid leukaemia (AML).

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 26 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: China 86+18503817651

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
Zhejiang Yangli Pharmaceutical Technology Co., Ltd.
Registry
ClinicalTrials.gov
Start date
30 October 2024
Est. completion
30 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The number of subjects with adverse events/serious adverse events; The number of subjects with dose-limiting toxicity (DLT), as defined in the protocol.

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: 26 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