Phase 2 Ovarian Cancer Trial, Recruiting NCT07480954 Sponsor: Beijing Biotech Condition: Ovarian Cancer
Back to Ovarian Cancer

Phase 2 Ovarian Cancer Trial, Recruiting

NCT07480954
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:

  • People who have been diagnosed with ovarian, fallopian tube, or primary peritoneal cancer that has been confirmed by laboratory testing of tissue (high-grade serous type is preferred).
  • People whose cancer has come back or stopped responding to treatment after at least two previous treatment courses, which should have included a platinum-based chemotherapy unless it was not medically suitable.
  • People whose cancer can be measured on scans according to a standard set of measurement rules called RECIST v1.1.
  • People whose tumor tissue (from a stored or fresh sample) shows high enough levels of at least two of the following proteins: mesothelin (MSLN), folate receptor alpha (FRα/FOLR1), or MUC16 (also known as CA-125).
  • People who are generally well enough to carry out everyday activities with no more than minor limitations, based on a standard doctor-assessed fitness scale (ECOG score of 0 or 1).
  • People whose blood counts and organ function meet certain minimum levels — including blood cell counts, liver function, kidney function, and bilirubin levels (confirm specific values with the trial site).
  • Women who could become pregnant must have a negative pregnancy test, and must agree to use effective contraception for 12 months after the treatment infusion, or as directed by local gene therapy guidelines.
  • People who are able to attend all required study visits and follow-up appointments, and who are willing to provide written consent to participate.

Who may not be able to join:

  • People who have received a gene-modified cell therapy — such as CAR-T or CAR-NK therapy — within the past 6 months, or who have previously received any therapy targeting the same proteins this trial targets (confirm details with trial site).
  • People who have active cancer spread to the brain or the lining around the brain or spinal cord that currently requires treatment.
  • People who have an active, uncontrolled infection, including active tuberculosis or a significant viral infection that is not under control.
  • People with HIV where the virus is not currently controlled, or who have active hepatitis B or hepatitis C with detectable virus levels at the time of screening.
  • People with serious heart conditions, such as a recent heart attack, a heart rhythm problem that is not controlled, or significant heart failure (confirm with trial site).
  • People who have an active autoimmune disease that required immune-suppressing medication within the past 30 days (low-dose steroid replacement therapy may still be acceptable — confirm with trial site).
  • People who are currently receiving other cancer treatments such as chemotherapy, targeted therapy, or radiation, or who have not waited long enough since stopping those treatments as required by the trial rules (confirm washout periods with trial site).
  • People who have had major surgery within 4 weeks before the start of the preparatory treatment phase of the trial (minor procedures may be acceptable — confirm with trial site).

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: +86 13076790030

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
Beijing Biotech
Registry
ClinicalTrials.gov
Start date
4 February 2026
Est. completion
17 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of dose-limiting toxicities (DLTs); Incidence and severity of treatment-emergent adverse events

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