68Ga-labeled NY105 PET Imaging in Patients

NCT05691881 | Unknown Early Phase 1

• 1 other identifier: LS2020004
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

This is a single arm study to evaluate the safety and biodistribution of 68Ga-labeled NY105 PET Imaging in patients

Conditions

Cancer

Outcome Measures

Primary Outcomes (1)

• Evaluation of tissue distribution of 68Ga-NY105

  Biodistribution of 68Ga-NY105 evaluated by radioactive uptake values (standardized uptake values, SUVs) in various organs during repeated 68Ga-PET scans will be reported.

  1 day

Study Arms (1)

68Ga-NY105

EXPERIMENTAL

Drug: 68Ga-NY105

Interventions

68Ga-NY105 DRUG

Patients will receive a tracer (20-40mcg, IV) dose of 68Ga (2-5mCi) labelled NY105

68Ga-NY105

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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\~3.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Affiliated Hospital of Jiangnan University: lead

Study Sites (1)

Affiliated Hospital of Jiangnan University

Wuxi, 214000, China

RECRUITING

MeSH Terms

Conditions

Neoplasms

Study Officials

• Chunjing Yu

  Affiliated Hospital of Jiangnan University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Chunjing Yu

CONTACT

15312238622; ycj_wxd1978@163.com

Study Design

• Study Type: interventional
• Phase: early phase 1
• Allocation: NA
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Director

Study Record Dates

• First Submitted: January 11, 2023
• First Posted: January 20, 2023
• Study Start: September 28, 2022
• Primary Completion: March 1, 2023
• Study Completion: September 1, 2023
• Last Updated: January 20, 2023

Record last verified: 2023-01

Locations

CN (1)