Study of CAR.5/IL15-transduced CB-NK cells for Blood Cancers

This study is testing a new treatment for certain blood cancers (hematological malignancies) that have come back or are not responding to standard treatments. The treatment involves giving you special immune cells called CAR.5/IL15-transduced CB-NK cells, along with chemotherapy drugs called Fludarabine Phosphate and Cyclophosphamide. Researchers want to find out how safe this treatment is, what dose works best, and how well it shrinks the cancer. To join, your cancer must show a certain level of a marker called CD5, and you must meet other specific criteria for your type of blood cancer. The main goal is to track any side effects you might experience.

Study design
This is an interventional study planning to enroll 64 participants. It is a Phase I/II study, meaning it will first look at safety and then at effectiveness.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed through study completion, which is an average of 1 year, to assess treatment-related side effects.

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

NCT05110742

Phase I/II Study of CD5 CAR Engineered IL15-Transduced Cord Blood-Derived NK Cells in Conjunction With Lymphodepleting Chemotherapy for the Management of Relapsed/Refractory Hematological Malignances

Recruiting
PHASE1Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~64 participants
Updated 2026-08-20 on ClinicalTrials.gov
What's tested:Fludarabine PhosphateCyclophosphamideCAR.5/IL15-transduced CB-NK cells

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE Version 5.0.
Measured over through study completion, an average of 1 year
Hematological Malignancy
1 sites across 1 states
Texas1
  • chitra hosing · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE Version 5.0.through study completion, an average of 1 year

    General grading: Grade 1: Mild: discomfort present with no disruption of daily activity, no treatment required beyond prophylaxis. Grade 2: Moderate: discomfort present with some disruption of daily activity, require treatment. Grade 3: Severe: discomfort that interrupts normal daily activity, not responding to first line treatment. Grade 4: Life Threatening: discomfort that represents immediate risk of death