← Eichor
Study identifier: NCT07589543 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Dual-Target CAR-NK Cells in Recurrent or Refractory Epithelial Ovarian Cancer

Condition: Epithelial Ovarian Cancer · Epithelial Ovarian Cancer, Fallopian Tube or Peritoneum  ·  Sponsor: Beijing Biotech

PhasePhase 1/Phase 2
Planned participants42
Who can joinFemale, 18 Years to 75 Years
Healthy volunteersNo

About this study

This study evaluates the safety, tolerability, and preliminary anti-tumor activity of EB-DUALNK, a dual-target chimeric antigen receptor natural killer (CAR-NK) cell therapy, in adults with recurrent or refractory epithelial ovarian cancer. Candidates for targeting include GD2, MUC1, PSMA, and mesothelin. After baseline biomarker assessment (tumor antigen expression), the program will select the most suitable dual-target pair for clinical testing. Participants will receive lymphodepleting chemotherapy followed by EB-DUALNK infusion and safety/response follow-up.

This description comes directly from the study's public registry record.

Talk to the study team

shan S Lu, Phd  ·  +86 13076790030  ·  Seni-Lu@beijing-biotech.com

Always discuss trial participation with your own doctor first.

Locations (1)

Peking University Shenzhen HospitalShenzhen, Guangdong, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07589543