First-in-human Study of Interferon-y PET Imaging to Assess Response to Immunotherapy
Launched by NERISSA T. VIOLA · May 28, 2024
Trial Information
Current as of August 19, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at a new imaging technique using a special agent called \[89Zr\]Zr-DFO-emapalumab to see how well immunotherapy works for patients with non-small cell lung cancer (NSCLC). The purpose is to use PET scans, which are detailed imaging tests, to find cancer lesions and check the patient's response to treatment. Participants will have a PET scan before starting immunotherapy and again about 30 days later to compare the results.
To join the study, patients must be at least 18 years old and have a confirmed diagnosis of non-small cell lung cancer, with at least one measurable tumor that is large enough to be seen on a PET scan. They should not have received any immunotherapy for their current cancer stage. Participants will need to complete some health checks before the imaging tests and must be able to stay still during the scans. This study is currently recruiting participants of all genders. If you or someone you know is interested, be sure to discuss it with the healthcare team for more details.
Gender
ALL
Eligibility criteria
- • Inclusion
- • Prior histologic or cytologic diagnosis of non-small cell lung cancer.
- • FDG PET done within 2 months of the baseline imaging, as part of standard-of-care.
- • measurable disease by RECIST 1.1 with at least one lesion of at least 2 cm in a region of the body that can be imaged by PET (e.g.,outside of the liver)
- • must be able to lie still for the tests. Their girth and weight must be suitable to enter the gantry, which varies per tomograph.
- • must be \>18 years old.
- • Patients must sign an informed consent indicating that they are aware of the investigational nature of this study, in keeping with the policies of the cancer center.
- • Physical exam, CBC and Multiphasic (including electrolytes, BUN, creatinine, total bilirubin, AST, and ALT) must be done within 28 days prior to PET imaging
- • Exclusion
- • No prior immunotherapy for current stage of NSCLC (Non Small Cell Lung Cancer). Immunotherapy in neoadjuvant or adjuvant setting and have recurrence at least 12 months following completion of immunotherapy are eligible after discussion with the principle investigator.
- • Pregnant or breast feeding individuals.
About Nerissa T. Viola
Nerissa T. Viola is a dedicated clinical trial sponsor with a commitment to advancing medical research and innovation. With extensive experience in the pharmaceutical and biotechnology sectors, Nerissa T. Viola focuses on developing and managing clinical trials that aim to assess the safety and efficacy of novel therapies. The organization prioritizes rigorous scientific methodologies and ethical standards, ensuring that all trials are conducted with the utmost integrity and compliance. Through collaboration with healthcare professionals and research institutions, Nerissa T. Viola strives to contribute to the improvement of patient outcomes and the overall advancement of medical science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Detroit, Michigan, United States
Patients applied
Trial Officials
Nerissa T Viola, PhD
Principal Investigator
Barbara Ann Karmanos Cancer Institute
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported