The Application of 18F-G1 PET/CT Targeting Granzyme B in the Pan-cancer Immunotherapy
Launched by PEKING UNIVERSITY FIRST HOSPITAL · Jun 17, 2025
Trial Information
Current as of June 28, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new type of imaging test called 18F-G1 PET/CT, which helps doctors see how well immunotherapy is working in patients with different types of cancer, including solid tumors (like lung or breast cancer) and blood cancers. Immunotherapy is a treatment that helps the body’s own immune system fight cancer. The goal is to find out if this imaging test can better track the effects of immunotherapy and help guide treatment decisions.
People who might join this study are adults diagnosed with cancer who have not had immunotherapy before and have at least one tumor that can be measured. They should be healthy enough to receive immunotherapy and expected to live at least six more months. Women who are pregnant or planning to become pregnant cannot join. Participants will undergo the 18F-G1 PET/CT scan during their immunotherapy treatment to help doctors monitor their progress. It’s important to know that this study has not started recruiting yet, and only those treated at certain centers where the scan can be done within a specific time frame will be eligible. Participants will need to agree to use contraception during and for six months after the study and provide informed consent before joining.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Subjects diagnosed with a malignant tumor by histopathology who are going to receive immunotherapy (monotherapy or combined immunotherapy) recommended by the multidisciplinary team.
- • 2. Subjects didn't receive previous immunotherapy.
- • 3. There exists at least one measurable target lesion according to the RECIST 1.1.
- • 4. ECOG performance status≤2.
- • 5. The expected survival time is ≥6 months.
- • 6. Effective contraceptive measures will be adopted during the study period and within 6 months after the study.
- • 7. Willing and able to fully understand and sign the informed consent form.
- Exclusion Criteria:
- • 1. Women in the preconception period, pregnancy, or lactation period.
- • 2. Combined with other malignant tumor.
- • 3. Diagnosed with autoimmune disease, or have long history of systemic steroid hormone therapy or immunosuppressive therapy.
- • 4. Having a history of severe cardiovascular disease, severe hepatic and renal insufficiency.
- • 5. Receiving radiotherapy or interventional therapy during the immunotherapy.
- • 6. 18F-G1 PET/CT or 18F-FDG PET/CT is not performed in our department, or the interval between baseline imaging and immunotherapy is more than 30 days.
About Peking University First Hospital
Peking University First Hospital is a leading medical institution in China, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a prominent sponsor of clinical trials, the hospital leverages its extensive expertise in various medical fields to conduct rigorous studies aimed at improving patient outcomes and contributing to global medical knowledge. With a multidisciplinary team of skilled researchers and clinicians, Peking University First Hospital is dedicated to the ethical conduct of clinical research, ensuring the highest standards of safety and efficacy in its trials. The institution plays a vital role in translating scientific discoveries into effective treatments, thereby enhancing the quality of care for patients both locally and worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported