Actively Recruiting

Early Phase 1
Age: 18Years - 90Years
All Genders
ID06632860

A Novel Dual-Targeting Molecular Probe TATE-RGD for Diagnosing Tumors Positive for SSTR2 and Integrin  23

Led by Peking Union Medical College Hospital · Updated on 2025-07-09

40

Participants Needed

1

Research Sites

1 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are evaluating a new dual-targeting molecular probe called 68Ga-TATE-RGD for imaging tumors that express somatostatin receptor 2 (SSTR2) and integrin  23. This study focuses on patients with tumors such as small cell lung cancer, pulmonary carcinoid, medullary thyroid cancer, and neuroendocrine tumors (NETs) that show positive expression of these receptors. The goal is to improve tumor detection and explore potential therapeutic uses of this dual-target tracer compared to existing single-target tracers. Participants will receive intravenous injections of the imaging agents 68Ga-TATE-RGD and 18F-FDG at specified doses for PET/CT and SPECT/CT scans. About 30 patients with confirmed positive expression of SSTR2 and integrin  23 will undergo imaging to assess the tracer's ability to detect tumors. The study is conducted under an early phase 1 protocol with no masking or blinding. During the study, patients will undergo PET/CT and SPECT/CT imaging within a week using the tracers. Researchers will measure tumor detection rates and standardized uptake values (SUV) over an average follow-up of half a year. Assessments include imaging evaluations and monitoring for any medical conditions affecting compliance. The total duration of participation varies but includes imaging and follow-up to evaluate diagnostic performance and tracer kinetics.

CONDITIONS

Brief Title

A Dual-targeting Tracer TATE-RGD for the Diagnosis of SSTR- and RGD- Positive Tumors

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed diagnosis of various cancers
  • Underwent 68Ga-TATE-RGD and 18F-FDG PET/CT scans within one week
  • Signed written informed consent
Not Eligible

You will not qualify if you...

  • Known allergy to TATE-RGD
  • Any medical condition that may significantly interfere with study compliance as judged by the investigator

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 1 week

Participants receive intravenous injections of 68Ga-TATE-RGD and 18F-FDG tracers and undergo PET/CT scans to image tumors positive for SSTR2 and integrin receptors.

2 visits (in-person) within one week

Long-term Monitoring

Duration - Approximately 6 months

Participants are monitored for tumor detection and tracer uptake values over approximately six months after imaging.

Follow-up visits as per clinical need

Trial Site Locations

Total: 1 location

1

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China, 010100

Actively Recruiting

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Research Team

Z

Zhaohui Zhu

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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