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Search / Trial NCT05835570

Integrin αvβ6-targeted PET in Malignant Tumors

Launched by ZHONGNAN HOSPITAL · Apr 18, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Non Small Cell Lung Cancer Breast Cancer Integrin αvβ6 [68 Ga]Ga Trivehexin Malignant Tumors

ClinConnect Summary

This clinical trial is studying a new imaging technique for detecting malignant tumors, which are dangerous cancers that can grow and spread in the body. The researchers are testing a special imaging agent called 68Ga-Trivehexin that targets a specific protein found mainly in cancer cells. This new approach aims to improve how doctors can see and evaluate tumors compared to the commonly used method, 18F-FDG PET imaging, which has some limitations. The goal is to find out if this new imaging probe can provide clearer and more accurate information about different types of tumors.

To participate in the trial, individuals must be between the ages of 65 and 74 and have a suspected or confirmed malignant tumor. It's important that participants are willing to sign a consent form to join the study. Women who are pregnant or planning to become pregnant within six months, as well as those with specific allergies or who have recently participated in other trials, are not eligible. If you join the trial, you can expect to undergo imaging tests to help researchers learn more about the effectiveness of this new method in detecting cancer.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participants with newly diagnosed malignant tumor confirmed by pathology or suspected lung cancer;
  • Age ≥18 years, regardless of gender;
  • No prior anti-tumor therapy (e.g., chemotherapy, radiotherapy, targeted therapy, or immunotherapy) before PET/CT;
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0-1;
  • Female subjects of reproductive age, male subjects and their partners agree to use reliable contraceptive measures (e.g., abstinence, birth control pills, injectable contraceptives, or subcutaneous contraceptive implants) until 6 months after the completion of the study;
  • Participants should voluntarily consent to the clinical trial, and have the ability to understand and sign an informed consent form.
  • Exclusion Criteria:
  • Known allergy to injection or its excipients;
  • Severe liver or renal dysfunction;
  • Claustrophobia or other psychiatric disorders;
  • History of other malignant tumors;
  • Participation in another clinical trial within 30 days prior to PET/CT scan;
  • Pregnant or breastfeeding women;
  • Refusal to participate or request for withdrawing from the clinical study;
  • Other conditions deemed unsuitable for inclusion by investigator.

About Zhongnan Hospital

Zhongnan Hospital, affiliated with Wuhan University, is a leading medical institution in China renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on multidisciplinary collaboration, the hospital employs state-of-the-art facilities and a team of highly skilled professionals to conduct rigorous clinical studies aimed at improving patient outcomes. Zhongnan Hospital prioritizes ethical standards and patient safety, ensuring adherence to regulatory requirements while fostering a culture of scientific excellence. As a prominent sponsor of clinical trials, the hospital plays a pivotal role in contributing to the global medical community and enhancing the understanding of various health conditions.

Locations

Wuhan, Hubei, China

Patients applied

0 patients applied

Trial Officials

Yong He, MD, PhD

Principal Investigator

Zhongnan Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported