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68Ga-NK224 PET Imaging of PD-L1 Expression in Cancers

Xiamen University logo

Xiamen University

Status

Enrolling

Conditions

PD-L1
Tumor

Study type

Observational

Funder types

Other

Identifiers

NCT06754345
XMYY-2023KY146

Details and patient eligibility

About

To evaluate the potential usefulness of 68Ga-NK224 positron emission tomography/computed tomography (PET/CT) for the evaluation of PD-L1 expression in primary and/or metastatic tumors, compared with histopathological results.

Full description

Participants with cancer underwent 68Ga-NK224 PET/CT for an initial assessment. Tumor uptake was quantified by the maximum standard uptake value (SUVmax) and mean SUV (SUVmean). In addition, the PD-L1 expression of lesions was confirmed by histopathological analyzing. The quantitative parameters of 68Ga-NK224 PET/CT were compared with histopathological result to evaluate the diagnostic efficacy.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • (i) adult patients (aged 18 years or order);
  • (ii) patients with newly diagnosed or previously treated malignant tumors (supporting evidence may include magnetic resonance imaging (MRI), CT, tumor markers and pathology report);
  • (iii) patients who had scheduled 68Ga-NK224 PET/CT scans;
  • (iv) patients who were able to provide informed consent (signed by participant, parent or legal representative) and assent according to the guidelines of the Clinical Research Ethics Committee.

Exclusion criteria

  • (i) patients with non-malignant lesions;
  • (ii) patients with pregnancy;
  • (iii) the inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.

Trial design

50 participants in 1 patient group

Experimental: 68Ga-NK224 PET/CT
Description:
Each participant receives a single intravenous injection of 68Ga-NK224, and undergo PET/CT imaging within the specified time.

Trial contacts and locations

1

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Central trial contact

Liang Zhao

Data sourced from clinicaltrials.gov

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