Phase 2 Ovarian Cancer Trial, Recruiting NCT07067255 Sponsor: Essen Biotech Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07067255
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:

  • Doctors expect you to live for at least 3 more months.
  • You have been diagnosed with ovarian cancer (including fallopian tube or peritoneal cancer) that has come back or stopped responding to standard treatments, confirmed by a tissue or cell sample test.
  • You have already received at least one round of platinum-based chemotherapy and your cancer has continued to grow, or your cancer does not respond well to platinum-based treatment, and there are no other standard treatments available that could cure it.
  • Your tumor tissue sample shows positive levels of two specific proteins (CD146 and GPC3) when tested in a lab — both must be present.
  • You have at least one area of cancer that can be clearly measured on a scan.
  • You are 18 years of age or older.
  • You are generally well enough to carry out daily activities, or only limited when it comes to strenuous physical effort (confirm with trial site).
  • Your heart, liver, kidneys, and bone marrow are working well enough to meet the trial's health requirements, including acceptable blood counts and organ function levels.
  • You are able to understand and sign a consent form and are willing to follow all trial procedures and attend follow-up visits.
  • If you are able to become pregnant, you must have a negative pregnancy test before joining and agree to use reliable contraception during the study and for a set period afterward.

Who may not be able to join:

  • You have previously received a CAR-T cell therapy or any other gene-engineered T-cell treatment targeting the same proteins (CD146 or GPC3).
  • You currently have active cancer spread to the brain or the lining around the brain and spinal cord (confirm with trial site if you have a history of treated brain metastases).
  • You have a serious, uncontrolled illness such as an active serious infection, significant heart failure, unstable heart condition, or a mental health or personal situation that would make it hard to follow the study requirements.
  • You have an active hepatitis B or C infection with detectable virus in your blood, or HIV with a viral level that is not controlled.
  • You need to take long-term medicines that suppress your immune system (for example, for an autoimmune disease or after an organ transplant), except for very low-dose steroids.
  • You are currently pregnant or breastfeeding, or you are able to become pregnant but are unwilling or unable to use adequate contraception.
  • You currently have another active cancer that requires treatment (some exceptions may apply — confirm with trial site).
  • You have a known severe allergic reaction to any part of the CAR-T cell treatment or to the chemotherapy drugs used to prepare your body before the treatment (cyclophosphamide or fludarabine).
  • Your doctor or the trial team feels that any other health condition makes you unsuitable for this study.

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 21 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: +12077706670

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
Essen Biotech
Registry
ClinicalTrials.gov
Start date
29 April 2025
Est. completion
10 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence and severity of dose-limiting toxicities (DLTs) following chemotherapy preparative regimen and infusion of GPC3/CD146 chimeric antigen receptor (CAR) T cells

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: 21 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