Actively Recruiting
PET Imaging Study of 68Ga-NB381 in Multiple Myeloma
Led by Peking University First Hospital · Updated on 2026-04-16
30
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Multiple myeloma (MM) predominantly affects the elderly, often presenting insidiously and with a rising incidence rate. Current diagnostic methods primarily rely on invasive bone marrow biopsies, which can lead to false-negative results if the biopsy site is improperly chosen. CD38 is significantly overexpressed on the surface of malignant plasma cells in MM, making it a characteristic tumor biomarker for this disease. Addressing the limitations in specificity and sensitivity of traditional PET imaging agents, this project is dedicated to developing a new type of nanobody PET/CT imaging probe, 68Ga-NB381, which possesses high affinity and targets CD38. This probe, which is an intellectual property of our institution, aims to enhance the accuracy and specificity of early MM diagnosis. In terms of clinical evaluation, the project will implement a comprehensive assessment process including case selection, collection of baseline information, high-precision imaging, expert-level image interpretation, and follow-up studies, comparing directly with traditional 18F-FDG imaging to thoroughly verify the specificity and safety of 68Ga-NB381. This lays the groundwork for the clinical translation of this radiopharmaceutical in China. Furthermore, the project contributes to formulating more effective precision treatment plans based on CD38 expression levels and provides evidence for monitoring the therapeutic effects of daratumumab, a drug also targeting CD38. This makes the project of significant academic value and clinical importance, thus promoting the development of personalized treatment strategies.
CONDITIONS
Official Title
PET Imaging Study of 68Ga-NB381 in Multiple Myeloma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients suspected of multiple myeloma scheduled for bone marrow aspiration or tissue biopsy within 3 months
- Age between 18 and 90 years
- Fully understand and voluntarily agree to participate and sign informed consent
- Able to comply independently with examination procedures
- Confirmed symptomatic multiple myeloma patients over 18 years
- Fully understand and voluntarily agree to participate and sign informed consent
- Able to comply independently with examination procedures
You will not qualify if you...
- Pregnant women
- Individuals unable to understand or cooperate with the examination process
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Peking University First Hospital
Beijing, Beijing Municipality, China, 100000
Actively Recruiting
Research Team
T
TIANYAO Wang, PhD
CONTACT
L
Lei Kang, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SEQUENTIAL
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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