Phase 3 Ovarian Cancer Trial, Recruiting NCT06394492 Sponsor: Suzhou Suncadia Biopharmaceuticals Co., Ltd. Condition: Ovarian Cancer
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Phase 3 Ovarian Cancer Trial, Recruiting

NCT06394492
Recruiting Phase 3

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 to take part and can sign a consent form agreeing to participate
  • You are a woman aged 18 or older
  • You have been diagnosed through testing with epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer
  • Your cancer has stopped responding to platinum-based chemotherapy (known as platinum-resistant disease)
  • You are able to provide a tumour tissue sample, either a fresh one or one stored from a previous procedure
  • You have at least one tumour that can be measured using standard imaging scans
  • You are generally able to carry out daily activities with no or only minimal limitations (confirm with trial site)
  • You are expected to live for at least 12 weeks or more
  • Your blood counts and organ functions (such as liver and kidneys) are at acceptable levels
  • You are willing and able to use contraception throughout the trial

Who may not be able to join:

  • You have uncontrolled fluid build-up around your lungs, heart, or abdomen that is causing symptoms
  • You have had or currently have another type of cancer
  • You have a history of, or currently have, a lung condition involving scarring or inflammation (confirm with trial site)
  • You have heart problems or heart disease that is not well controlled
  • You have had a blood clot in an artery or vein before starting the trial
  • You have had a significant bleeding event before starting the trial (confirm with trial site)
  • You have had a hole or abnormal opening in your digestive tract, a urinary tract opening, or an infection/abscess in your abdomen before starting the trial
  • You have a bowel blockage or are being fed through an intravenous line instead of eating normally
  • You have had a serious infection before starting the trial
  • You have active hepatitis B or hepatitis C infection
  • You have received cancer treatment within 4 weeks before starting the trial
  • You have previously been treated with a specific type of chemotherapy drug called a TOP1 inhibitor, or a drug that delivers a TOP1 inhibitor directly to cancer cells
  • You still have significant side effects (grade 2 or higher) from a previous cancer treatment that have not resolved (confirm with trial site)
  • You have had a severe allergic reaction to the study drug (SHR-A1921) or any of its ingredients
  • The trial doctor has another reason they feel makes you unsuitable for the trial

⚠️ 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 30 June 2026
Phase 3: approximately ~65% 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Registry
ClinicalTrials.gov
Start date
10 May 2024
Est. completion
31 May 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free Survival (PFS) assessed by Blinded Independ Review Committee (BIRC) as per RECIST 1.1

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: 30 June 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