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Clinical Trials in China / NCT07782944
Recruiting Not applicable

CD38 Targeted -PET/ CT for Multiple Myeloma

NCT07782944 · tracked via the Priya Life Science China tracker
Sponsor
Guilin Medical University, China
Phase
Not applicable
Started
2026-07-07
Last updated
2026-08-24

Condition(s) studied

Multiple Myeloma (MM), Lymphoma, Large B-Cell, Diffuse (DLBCL), Lymphoma

Investigational drug(s) / intervention(s)

standard-of-care imaging (FDG PET/CT), CD38 PET/CT

standard-of-care imaging (FDG PET/CT), CD38 PET/CT: Each subject receives a single intravenous injection of standard-of-care imaging radiopharmaceutical (FDG) and CD38, and undergoes PET/CT imaging within the specified time.

Study summary

The objective of the study is to construct a noninvasive approach CD38 targeted PET/CT to detect tumor lesions in patients with Multiple Myeloma and to compare with FDG PET/CT.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients (aged 18 years or older); * Patients with newly diagnosed, highly suspected recurrence or previously treated metastases of Multiple Myeloma (supporting evidence may include MRI, CT, tumor markers, and pathology report); * Patients who had scheduled both standard-of-care imaging (FDG PET/CT) and cd38 PET/CT scans; * 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: * The inability or unwillingness of the research participant or legal representative to provide written informed consent.

Primary outcome measure(s)

  • Diagnostic efficacy — 3 year
    The sensitivity, specificity, and accuracy of standard-of-care imaging (FDG PET/CT) and CD38 PET/CT were calculated and compared to evaluate the diagnostic accuracy.

Trial sites (1)

FacilityCityRegionStatus
The First Affliated Hospital of Guilin Medical University Guilin Guangxi Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07782944 on ClinicalTrials.gov ↗ ← All trials in China