First-in-human Study of Interferon-y PET Imaging to Assess Response to Immunotherapy

Recruiting Phase 1 Interventional Study
Non Small Cell Lung Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Diagnostic
Participants needed
6 (estimated)
Sponsor
Nerissa T. Viola · Other
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About This Trial

The goal of this clinical trial is to investigate the use of \[89Zr\]Zr-DFO-emapalumab as an IFN-γ PET imaging agent to detect lesions and response to therapy among treatment-naïve non-small cell lung cancer (NSCLC) patients. PET scans following the imaging agent will be completed prior to and about 30 days after starting immunotherapy.

Trial Locations
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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…
Contacts

Nerissa T Viola, PhD

3135768309

violan@karmanos.org

CONTACT