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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05638256
Other study ID # LS2020003
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date October 10, 2022
Est. completion date October 2023

Study information

Verified date November 2022
Source Affiliated Hospital of Jiangnan University
Contact Chunjing Yu
Phone 15312238622
Email ycj_wxd1978@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a single arm study to evaluate the safety and biodistribution of 68Ga-labeled NY104 PET Imaging in patients with Renal Cell Carcinoma


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date October 2023
Est. primary completion date October 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Patients voluntarily signed informed consent; 2. Age 18-75, male or female; 3. Patients diagnosed with renal cell carcinoma confirmed by histopathology or cytology; 4. At least one measurable solid lesion has been examined according RECIST1.1 standard; 5. ECOG score 0~3; Life expectancy of at least 3 months; Exclusion Criteria: 1. Recovery from major trauma (including surgery) within 4 weeks prior to study treatment; 2. Patients with systemic or locally severe infections, or other serious coexisting diseases; 3. Patients with abnormal immune function or who have recently used immunosuppressive or potentiating agents including various vaccines; 4. Patients with autoimmune diseases, including rheumatoid arthritis; 5. Inadequate control of arrhythmias, including atrial fibrillation; 6. Uncontrolled hypertension; 7. Patients with allergies or allergies to any component of the imaging agent or antibody; 8. Patients who cannot undergo PET/CT imaging scan; 9. Syphilis, HBV, HCV, or HIV positive subjects; 10. Male and female subjects of reproductive age cannot take effective contraceptive measures; 11. Pregnant or lactating women; 12. Patients with a history of mental illness or related conditions; 13. Other subjects considered unsuitable by researchers.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
68Ga-NY104
Patients will receive a tracer (20-40mcg, IV) dose of 68Ga (2-5mCi) labelled NY104

Locations

Country Name City State
China Affiliated Hospital of Jiangnan University Wuxi Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Affiliated Hospital of Jiangnan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of tissue distribution of 68Ga-NY104 Biodistribution of 68Ga-NY104 evaluated by radioactive uptake values (standardized uptake values, SUVs) in various organs during repeated 68Ga-PET scans will be reported. 1 year
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