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Chemokine Receptor 4 PET/CT Imaging of CXCR4-Related Diseases

T

Tianjin Medical University

Status

Enrolling

Conditions

Metastasis
CXCR4-related Disease
Tumor
Positron Emission Tomography

Treatments

Diagnostic Test: CXCR4 PET/CT Imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT06690736
TJMUGH-02

Details and patient eligibility

About

To evaluate the potential usefulness of 68Ga/18F-Pentixafor/Pentixather positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various CXCR4-related disease patients.

Full description

Subjects with various CXCR4-related disease patients underwent 68Ga/18F-Pentixafor/Pentixather PET/CT either for an initial assessment or for recurrence detection. Lesions uptake was quantified by the maximum standard uptake value (SUVmax). The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy of 68Ga/18F-Pentixafor/Pentixather PET/CT were calculated.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • suspected or confirmed untreated Lymphoproliferative and other CXCR4-related diseases patients
  • 18F-FDG PET/CT within two weeks
  • signed written consent.

Exclusion criteria

  • pregnancy
  • breastfeeding
  • known allergy against Pentixafor

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

CXCR4 PET/CT Imaging
Experimental group
Description:
Intravenous injection of one dose of 2-5 mCi 68Ga/18F-Pentixafor/Pentixather. Tracer doses of radiotracers will be used to image lesions by PET/CT
Treatment:
Diagnostic Test: CXCR4 PET/CT Imaging

Trial contacts and locations

1

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Central trial contact

Haonan Yu, MD; Shaobo Yao, PhD

Data sourced from clinicaltrials.gov

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