Actively Recruiting

Early Phase 1
Age: 18Years - 70Years
FEMALE
Healthy Volunteers
NCT06411678

Application of 68GA-labeled CD73 Targeting Probe PET/CT Imaging in the Diagnosis of Breast Cancer

Led by Peking Union Medical College Hospital · Updated on 2025-06-17

50

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators plan to conduct a 68Ga-DOTA-dPNE PET/CT imaging study in breast cancer patients to observe the binding of the tracer to tumor lesions and evaluate CD73 expression. As part of the study design, a subset of patients will initially undergo dynamic PET/CT imaging to evaluate the safety profile and pharmacokinetic distribution of the radiotracer in vivo. Subsequently, static PET/CT imaging will be performed on additional patients to assess the diagnostic effectiveness of 68Ga-DOTA-dPNE. Imaging results will be correlated with relevant clinical indicators to evaluate the potential of this tracer in diagnosing breast cancer, guiding therapeutic decisions, and predicting responses to targeted therapies.

CONDITIONS

Official Title

Application of 68GA-labeled CD73 Targeting Probe PET/CT Imaging in the Diagnosis of Breast Cancer

Who Can Participate

Age: 18Years - 70Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients aged 18 years or older
  • Expected survival of at least 12 weeks
  • No prior radiotherapy or chemotherapy
  • Surgery or biopsy feasible for pathological diagnosis
  • At least one measurable target lesion as defined by RECIST v1.1
  • Able to provide written informed consent and comply with follow-up requirements
Not Eligible

You will not qualify if you...

  • Severe liver or kidney dysfunction
  • Pregnant, breastfeeding, planning to become pregnant, or planning to have children during the study period
  • Women of childbearing potential must use effective contraception during the study
  • Unable to lie flat for 30 minutes
  • History of claustrophobia or other psychiatric disorders
  • Any other condition deemed unsuitable for participation by the investigator
  • Refusal to participate in the clinical study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

PUMCH

Dongcheng, Beijing Municipality, China, 100730

Actively Recruiting

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Research Team

C

Chenhao JIA

CONTACT

X

Xianzhong ZHANG

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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