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Phase 1RecruitingPriority 4 · Lower priorityNCT06696846

CD70-CAR-NK Cell Therapy for T Cell Lymphoma and Acute Myeloid Leukemia

ClinicalTrials.gov

Plain-language summary

This Phase 1 trial is evaluating CD70 CAR-NK as a treatment for people newly diagnosed with a type of T-cell lymphoma called AITL. The study starts with lower doses to find the safest effective dose before testing in more people. This trial does not currently list US sites.

Who can join (key eligibility)

  • Age 18 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

CD70 CAR-NK (BIOLOGICAL): CAR - NK cells constructed by using genetic engineering technology retain the original extensive tumor - killing ability of NK cells. By using their unique target cell recognition mechanism, the target is accurately locked on specific antigen proteins, thereby enhancing the anti - tumor effect. Cord blood-derived CAR - NK cell products shorten the treatment time and are inexpensive. Multiple studies have confirmed the feasibility of CAR - NK cells in treating hematological tumors. Blocking the CD70/CD27 signaling pathway plays an important role in inhibiting CD70 - positive tumors, such as refractory/relapsed T - cell lymphoma and acute myeloid leukemia. Pre - clinical studies in our laboratory have proved that CD70 CAR - NK can effectively inhibit the in - vivo and in - vitro proliferation of T - cell lymphoma and prolong survival.

Drugs / treatments
CD70 CAR-NK
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 1
Status
Recruiting
Design
Non-randomized, open-label
Enrollment target
25 patients
Primary endpoint
The incidence and type of dose-limiting toxicity (DLT) within 28 days; the incidence and severity of treatment-related adverse events as assessed by CTCAE v4.0
Ages
18 Years to 75 Years
Start date
2024-12-01
Est. completion
2028-11-30

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University (OTHER)
Contact
Wenbin Qian | qianwb@zju.edu.cn | +86 0571 87783759

Tags

AITL/TFHALCL ALK−MaintenanceNewly diagnosedRelapsed/Refractory
TrialCompass — Clinical Trial Summary

CD70-CAR-NK Cell Therapy for T Cell Lymphoma and Acute Myeloid Leukemia

NCT06696846

Phase: Phase 1 | Status: Recruiting | Priority: Lower

Plain-language summary

This Phase 1 trial is evaluating CD70 CAR-NK as a treatment for people newly diagnosed with a type of T-cell lymphoma called AITL. The study starts with lower doses to find the safest effective dose before testing in more people. This trial does not currently list US sites.

Who can join

  • Age 18 Years to 75 Years years
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

CD70 CAR-NK (BIOLOGICAL): CAR - NK cells constructed by using genetic engineering technology retain the original extensive tumor - killing ability of NK cells. By using their unique target cell recognition mechanism, the target is accurately locked on specific antigen proteins, thereby enhancing the anti - tumor effect. Cord blood-derived CAR - NK cell products shorten the treatment time and are inexpensive. Multiple studies have confirmed the feasibility of CAR - NK cells in treating hematological tumors. Blocking the CD70/CD27 signaling pathway plays an important role in inhibiting CD70 - positive tumors, such as refractory/relapsed T - cell lymphoma and acute myeloid leukemia. Pre - clinical studies in our laboratory have proved that CD70 CAR - NK can effectively inhibit the in - vivo and in - vitro proliferation of T - cell lymphoma and prolong survival.

Drugs / treatments: CD70 CAR-NK

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 25 patients

Primary endpoint: The incidence and type of dose-limiting toxicity (DLT) within 28 days; the incidence and severity of treatment-related adverse events as assessed by CTCAE v4.0

Ages: 18 Years to 75 Years

Start date: 2024-12-01 | Est. completion: 2028-11-30

Locations

0 US sites · 1 total

Contact

Wenbin Qian | qianwb@zju.edu.cn | +86 0571 87783759

Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University (OTHER)

Tags

AITL/TFH · ALCL ALK− · Maintenance · Newly diagnosed · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06696846

Prepared using TrialCompass (trialcompass.com) on July 4, 2026. For informational purposes only. Always discuss with your healthcare team.
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Data sourced from ClinicalTrials.gov.

For informational purposes only. Not medical advice — always consult your healthcare team.

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Data last updated: June 2026

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