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Clinical Study of NKG2D CAR-NK Combined with PD-1 Monoclonal Antibody in the Treatment of ATC

Clinical Exploratory Study of NKG2D CAR-NK Combined with PD-1 Monoclonal Antibody in the Treatment of Anaplastic Thyroid Cancer (ATC)

Status
Not yet recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06856278
Enrollment
30
Registered
2025-03-04
Start date
2025-02-22
Completion date
2029-03-01
Last updated
2025-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaplastic Throid Carcinoma

Brief summary

The patients with anaplastic thyroid cancer were treated with CAR-NK immune cells combined with PD-1 monoclonal antibody, and the safety and tolerability of the patients were observed and evaluated.

Interventions

DRUGNKG2D CAR-NK with PD-1 Antibody

Treated with CAR-NK immune cells combined with PD-1 monoclonal antibody.

Sponsors

Zhejiang Provincial People's Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18-75 years (including boundary values), male or female. 2. Be diagnosed with anaplastic thyroid cancer histopathologically with a measurable lesion≥1cm. 3. Liver and kidney function is good, and can tolerate treatment. 4. Be able to cooperate with the completion of treatment and follow-up work. 5. No other systemic diseases, including other malignancies.

Exclusion criteria

1. Need to breastfeed the baby or have fertility needs; 2. Immune system diseases; 3. Diseases of the blood system; 4. Mental system diseases; 5. Interstitial pneumonia, lung disease, etc.; 6. Failure to follow rules of this study.

Design outcomes

Primary

MeasureTime frameDescription
Safety and tolerabilityFrom the start of the trial to day 56 after the first infusion of CAR-NK.Safety and tolerability at 28 days after combination therapy, dose limiting toxicity (DLT) and maximum tolerated dose (MTD) were determined.

Countries

China

Contacts

Primary ContactMinghua Ge
geminghua@hmc.edu.cn+86-0571 87666666

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026