Nectin-4 Specific LMW PET Probe Imaging in Urothelial Carcinoma

Last updated: August 16, 2024
Sponsor: Peking University Cancer Hospital & Institute
Overall Status: Active - Recruiting

Phase

N/A

Condition

Urothelial Carcinoma

Carcinoma

Treatment

18F-FDG

Clinical Study ID

NCT05321316
2022KT37
  • Ages 18-75
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

To evaluate the ability of [68Ga]N188 to detect nectin-4 overexpression in patients with urothelial carcinoma, especially in patients with recurrent or advanced bladder cancer.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. 18-75 years old, male or female;

  2. Heart function is normal;

  3. Normal heart function;

  4. Estimated survival ≥12 weeks;

  5. Good follow-up compliance;

  6. presence of at least one measurable target lesion according to RECIST1.1 criteria;

  7. Women of childbearing age (15-49 years) must have a negative pregnancy test within 7days before starting the test; Fertile men and women must agree to use effectivecontraception to prevent pregnancy during the study period and for 3 months afterthe test;

  8. Patients recommended by clinicians to undergo PET/CT examination for tumordiagnostic staging;

  9. The subject patients could fully understand and voluntarily participate in theexperiment, and signed the informed consent.

Exclusion

Exclusion Criteria:

  1. Serious abnormality of liver, kidney and blood;

  2. Pregnant patients;

  3. Pregnant and lactation women;

  1. unable to lie flat for half an hour; 4) Refuse to join the clinical investigator; 5)Suffering from claustrophobia or other mental diseases; 6) Other conditions thatresearchers deem unsuitable for participating in the experiment.

Study Design

Total Participants: 20
Treatment Group(s): 1
Primary Treatment: 18F-FDG
Phase:
Study Start date:
May 31, 2022
Estimated Completion Date:
December 31, 2024

Connect with a study center

  • Beijing Cancer Hospital

    Beijing, Beijing 100142
    China

    Active - Recruiting

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