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Radiolabelled Nectin-4 Targeted LMW Probe PET/CT in Patients With Lung Lesions

P

Peking University Cancer Hospital & Institute

Status

Enrolling

Conditions

Lung Infection
Lung Cancer, Non-Small Cell

Treatments

Other: FDG-PET

Study type

Observational

Funder types

Other

Identifiers

NCT06648317
2022KT37-ZY01-1

Details and patient eligibility

About

To evaluate the ability of [68Ga]N188 to detect nectin-4 overexpression in patients with lung lesions.

Full description

To evaluate the ability of [68Ga]N188 to detect nectin-4 overexpression in patients with different lung lesions, such as inflammation and lung cancer.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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 7 days before starting the test; Fertile men and women must agree to use effective contraception to prevent pregnancy during the study period and for 3 months after the test;
  8. Patients recommended by clinicians to undergo PET/CT examination for tumor diagnostic staging;
  9. The subject patients could fully understand and voluntarily participate in the experiment, and signed the informed consent.

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 that researchers deem unsuitable for participating in the experiment.

Trial contacts and locations

1

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Central trial contact

Nan Li; Xin Zhou, MD

Data sourced from clinicaltrials.gov

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