← Eichor
Study identifier: NCT06659653 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Safety and Efficacy of PRG-2302 for Refractory or Relapsed B-cell Acute Lymphoblastic Leukemia Disease.

Condition: Acute Lymphoblastic Leukemia  ·  Sponsor: Tan Jie

PhaseEARLY_Phase 1
Planned participants18
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

A Clinical Study on the Safety and Effectiveness of CD19/CD22 Chimeric Antigen Receptor T Cells in the Treatment of Refractory or Relapsed B-cell Acute Lymphoblastic Leukemia Disease.

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

Talk to the study team

Tan jie  ·  18163137226  ·  alooof@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First People's Hospital of JingzhouJinzhou, Hubei, 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/NCT06659653