Phase 3 Ovarian Cancer Trial, Recruiting
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Progression-free Survival (PFS) assessed by Blinded Independ Review Committee (BIRC) as per RECIST 1.1
Can't join this trial?
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.