Fact CheckerSign in

NCT06717113RecruitingEarly phase 1

A Molecular Probe Targeting BCMA for the Clinical Diagnosis of Multiple Myeloma

Clinical PET Imaging Evaluation of 68Ga-BC1 Probe in Multiple Myeloma

Source: ClinicalTrials.gov · Last updated 6 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Multiple Myeloma (MM), the second most common hematological malignancy, continues to pose challenges in precise clinical identification. As a potential solution, nuclear medicine immuno-PET imaging has emerged as a promising approach. However, traditional full-length antibody probes suffer from delayed tumor uptake peaks and low target-to-background ratios, limiting their clinical utility. In our study, a peptide or nanobody targeting BCMA was developed by computer-aided designing, which was subsequently radiolabeled with 68Ga to create a novel molecular probe, 68Ga-MM-BC1. This research aims to overcome the diagnostic limitations of MM and may also offer valuable insights for molecular-targeted imaging in other malignant tumors.

Status (registry)
Recruiting
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
50 (estimated)
First submitted
28 Sept 2024
Start date
15 Apr 2025
Primary completion date
31 Dec 2025
Lead sponsor
Peking University First Hospital
NCT number
NCT06717113

What you commit to

  • Study type: Interventional · Early phase 1
  • Planned participants: 50
  • From 15 Apr 2025 to the primary completion date, 31 Dec 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnant women; individuals unable to understand the examination process or who are unable to cooperate.

Who the study is looking for

  • Suspected multiple myeloma patients scheduled for bone marrow aspiration or tissue biopsy within the past 3 months; able to fully understand and voluntarily participate in the study, with signed informed consent; able to cooperate with the examination.
  • Diagnosed symptomatic multiple myeloma patients; able to fully understand and voluntarily participate in the study, with signed informed consent; able to cooperate with the examination.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University First Hospital
Coordinator of this site? Confirm its status
BeijingChinaEnrolling by invitation
Department of Nuclear Medicine, Peking University First Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.