Chimeric Antigen Receptor Treatment Targeting CD70 (SEVENTY) for Leukemia

This study is for people up to 75 years old with certain types of leukemia (blood cancer) that have come back or haven't responded to standard treatments. Specifically, it's for acute myeloid leukemia (AML), T-cell leukemia, or B-cell leukemia where the cancer cells have a protein called CD70. You would receive a single infusion of special immune cells, called T cells, that have been modified to recognize and fight cancer cells with CD70. The study aims to find the safest dose of these modified T cells, called CD70.CAR T cells, by looking at any serious side effects within the first four weeks after treatment. This treatment uses your own immune system to target the cancer.

Study design
This is an interventional study with a planned enrollment of 12 participants. It involves different dose levels of the CD70.CAR T cell infusion.
What's involved
You will provide blood to create the special T cells for your treatment. These cells will be prepared and then given back to you as a single infusion.
Compensation
Not stated in the trial record.
Follow-up
The main safety outcome will be measured for four weeks after the infusion.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06345027

Chimeric Antigen Receptor Treatment Targeting CD70 (SEVENTY)

Not Yet Recruiting
PHASE1Up to 75InterventionalTreatment
Baylor College of Medicine
~12 participants
Updated 2025-12-16 on ClinicalTrials.gov
What's tested:Treatment Arm A

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Dose limiting toxicity (DLT) rate
Measured over Time Frame 4 weeks post infusion
Leukemia, Myeloid, Acute
Leukemia, B-cell
Leukemia, T-Cell
2 sites across 1 states
Texas2
  • Bilal Omer, MD · PRINCIPAL_INVESTIGATOR · Baylor College of Medicine

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

PT and aPTT \<1.5x ULN
Serum Creatinine \< 2 x ULN
AST \< 5 x ULN 6. Informed consent
  • Dose limiting toxicity (DLT) rateTime Frame 4 weeks post infusion

    1\. Dose-limiting toxicity (CTCAE v5.0) is defined as any grade 3 or 4 non-hematologic toxicities (including allergic reactions and ICANS) that fails to return to Grade 2 within 72 hours or any grade 5 toxicity (additional assessment criteria may apply).