RecruitingNot ApplicableNCT05436093
CLDN18.2 Targeting Nanobody Probe for PET Imaging in Solid Tumors
Sponsor
Peking University Cancer Hospital & Institute
Enrollment
15 participants
Start Date
Jun 23, 2022
Study Type
INTERVENTIONAL
Conditions
Summary
The objective of the study is to construct a noninvasive approach 68Ga-ACN376 PET/CT to detect the CLDN18.2 expression of tumor lesions in patients with Solid tumors and to identify patients benefiting from CLDN18.2 targeting treatment.
Eligibility
Min Age: 18 YearsMax Age: 75 Years
Inclusion Criteria4
- \. Aged >18 years old; ECOG 0 or 1;
- \. Patients with solid tumors;
- \. Has at least one measurable target lesion according to Response Evaluation Criteria in Solid Tumors (RECIST V1.1);
- \. life expectancy >=12 weeks.
Exclusion Criteria6
- \. Significant hepatic or renal dysfunction;
- \. Is pregnant or ready to pregnant;
- \. Cannot keep their states for half an hour;
- \. Refusal to join the clinical study;
- \. Suffering from claustrophobia or other mental diseases;
- \. Any other situation that researchers think it is not suitable to participate in the experiment.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
DRUG18F-FDG
All study participants will undergo one 18F-FDG PET/CT scan.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05436093
Related Trials
NCI Childhood Cancer Data Initiative (CCDI) Led Pediatric, Adolescent, and Young Adult Rare Cancer Registry for Very Rare Solid Tumors
NCT074893781 location
A Study to Find a Suitable Dose of ASP5834 in Adults With Solid Tumors
NCT0709420418 locations
Study to Evaluate IMGS-001 Treatment in Patients With Relapsed or Refractory Advanced Solid Tumors
NCT060145026 locations
Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors
NCT075171982 locations
A Clinical Study of HRS-8364 in the Treatment of Advanced Solid Tumor Subjects
NCT074461532 locations