CAR.70-Engineered NK Cells for Relapsed/Refractory Blood Cancers

This study is testing a new way to treat blood cancers like B-Cell Lymphoma, Myelodysplastic Syndromes (MDS), Acute Myeloid Leukemia (AML), Multiple Myeloma, and Plasma Cell Leukemia. It uses special immune cells called natural killer (NK) cells that have been engineered to target cancer. These CAR.70/IL15-transduced CB-NK cells are given through an IV, along with chemotherapy drugs called Cyclophosphamide and Fludarabine phosphate. Researchers want to see how safe this treatment is and how well it works. To join, your tumor must show a certain level of a marker called CD70. Success in this study means seeing if the treatment causes side effects, if your cancer shrinks or disappears, and if you remain alive and in remission after treatment.

Study design
This is an interventional study planning to enroll 80 participants. It is designed to evaluate the safety and effectiveness of the treatment.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Researchers will monitor participants for treatment-related side effects throughout the study (about 1 year), check for cancer response up to 30 days after the last treatment, and track if participants are alive and in remission for up to 180 days.

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NCT05092451

Phase I/II Study of CAR.70- Engineered IL15-transduced Cord Blood-derived NK Cells in Conjunction With Lymphodepleting Chemotherapy for the Management of Relapse/Refractory Hematological Malignances

Recruiting
PHASE1Ages 12–80InterventionalTreatment
M.D. Anderson Cancer Center
~80 participants
Updated 2026-08-07 on ClinicalTrials.gov
What's tested:CyclophosphamideCAR.70/IL15-transduced CB-NK cellsFludarabine phosphate

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
+2 more outcomes measured
B-Cell Lymphoma
Myelodysplastic Syndromes (MDS)
Acute Myeloid Leukemia (AML)
Multiple Myeloma
Plasma Cell Leukemia
Hodgkin Lymphoma
T-cell Non-Hodgkin's Lymphoma/ T-cell Acute Lymphoblastic Leukmeia
Myelodysplastic Syndrome / Chronic Myelomonocytic Leukemia
Blastic Transformation of Chronic Myeloid Leukemia
Germ Cell Tumors
1 sites across 1 states
Texas1
  • David Marin, MD · 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

    CTCAE Version 5.0 - 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

  • Number of Participants with Complete or Partial ResponseUp to 30 days after the last treatment
  • Number of Participants who are Alive and in RemissionUp to 180 days

    Number of Participants who are Alive and in Remission after 6 months.