Phase 2 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:
- Women aged 18 or older who have signed the written consent form
- Women with a general health status rated as fully active or restricted only in physically strenuous activity (this is measured using a standard scale called ECOG, scored 0 or 1)
- People with a life expectancy of at least 3 months
- People diagnosed with a specific type of ovarian cancer (epithelial, non-mucinous) — this includes ovarian, fallopian tube, or primary peritoneal cancer — where the cancer came back or grew more than 6 months after the last dose of platinum-based chemotherapy
- People who carry a BRCA gene mutation must have previously received a type of treatment called a PARP inhibitor before joining (confirm with trial site)
- People whose cancer can be measured on scans according to standard criteria used by the trial team
- People who are able to provide a stored tumour tissue sample (a preserved tissue block from a previous biopsy or surgery)
- People whose liver, kidneys, and other organs are functioning at an adequate level
- People of reproductive potential who agree to use effective contraception during the trial and for 6 months after the last dose of treatment
Who may not be able to join:
- People with certain other types of ovarian tumours, such as mucinous cancer or sex cord stromal cell tumours
- People who have cancer that has spread to the brain or the lining of the brain or spinal cord
- People with fluid build-up around the lungs, heart, or abdomen that cannot be controlled and needs repeated draining
- People who have had another active cancer within the past 3 years
- People who have received systemic cancer treatment within 2 weeks before joining the trial
- People who have previously received treatments that work by targeting the immune system's response to tumours
- People who have had major surgery, an open biopsy, or a significant injury within 4 weeks before joining, or who are expected to need major surgery during the trial
- People with an active or recurring autoimmune disease (a condition where the immune system attacks the body's own tissues)
- People who need regular high-dose steroid medication or other immune-suppressing drugs within 14 days before joining (confirm with trial site for specific dosage thresholds)
- People who have received a live vaccine within 4 weeks before joining
- People with a known condition that weakens the immune system, including those who test positive for HIV
- People with a history of receiving a donated organ or donated stem cell transplant
- People with a known history of interstitial lung disease or non-infectious lung inflammation
- People with a serious infection that required or requires hospitalisation
- People with an active infection currently requiring treatment
- People with active hepatitis B or active hepatitis C
- People with active inflammatory bowel disease or active diverticulitis (inflammation of pouches in the bowel)
- People with significant heart or blood vessel disease (confirm with trial site for specific conditions)
- People who still have unresolved side effects from previous cancer treatment
- People with a history of severe allergic reactions to monoclonal antibody treatments (a type of targeted therapy)
- Women who are pregnant or breastfeeding
- People with any other condition that the trial doctor believes may make it unsafe to receive the study drug
- People with a known allergy or medical reason to avoid paclitaxel or carboplatin (relevant to certain groups within the trial)
- People with a known allergy or medical reason to avoid Olaparib (relevant to certain groups within the trial)
- People with a known allergy or medical reason to avoid any component of the study drug AK112, or a medical condition that affects its safety
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.
Contact this trial
Phone: (0760)89873999
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
Where this trial is recruiting
Primary endpoints
Progression-free survival (PFS) assessed by investigator per RECIST v1.1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.