89Zr-labeled NY009 PET Imaging in Patients

This is a single arm study to evaluate the safety and biodistribution of 89Zr-labeled NY009 PET Imaging in patients

Inclusion Criteria:Patients voluntarily signed informed consent;Age 18-75, male or female;Patients diagnosed with cancer confirmed by histopathology or cytology;At least one measurable solid lesion has been examined according RECIST1.1 standard;ECOG score 0~2.Exclusion Criteria:Recovery from major trauma (including surgery) within 4 weeks prior to study treatment;Patients with systemic or locally severe infections, or other serious coexisting diseases;Patients with abnormal immune function or who have recently used immunosuppressive or potentiating agents including various vaccines;Patients with autoimmune diseases, including rheumatoid arthritis;Inadequate control of arrhythmias, including atrial fibrillation;Uncontrolled hypertension;Patients with allergies or allergies to any component of the imaging agent or antibody;Patients who cannot undergo PET/CT imaging scan;Syphilis, HBV, HCV, or HIV positive subjects;Male and female subjects of reproductive age cannot take effective contraceptive measures;Pregnant or lactating women;Patients with a history of mental illness or related conditions;Other subjects considered unsuitable by researchers.