The aim of this Phase 2 study is to investigate the efficacy and safety of a single dose
of LS301-IT, a novel fluorescence imaging agent developed by Integro Theranostics (IT),
administered by intravenous (IV) infusion in patients undergoing VATS (Video-Assisted
Thoracoscopic Surgery) or RATS (Robotic-Assisted Thoracoscopic Surgery) resection of
Stage I-II non-small cell lung cancer (NSCLC).
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07276789.
Locations matching your search criteria
United States
Pennsylvania
Philadelphia
University of Pennsylvania/Abramson Cancer CenterStatus: Active
Name Not Available
The primary objective of the study is to determine the proportion of subjects that have
at least one Clinically Significant Event (CSE) using fluorescence imaging, defined as
either the localization of the primary tumor when white light has failed to identify the
tumor, the identification of a synchronous or occult pulmonary tumor with fluorescence
only, or the identification of an inadequate surgical margin after resection. Secondary
objectives include the determination of the sensitivity and positive predictive value
(PPV) of LS301 fluorescence imaging in the identification of tumor using histopathology
as the gold standard, and the assessment of the safety and tolerability of LS301-IT.
Exploratory objectives include the determination of the "Clinical Impact Rate" defined as
the proportion of cases when the surgeon changes the scope of the procedure based on
LS301 fluorescence imaging, the assessment of the dosing interval prior to surgery, and
the standardization of imaging during surgery and surgeon assessment of fluorescence.
Lead OrganizationIntegro Theranostics
Principal InvestigatorRobert Honigberg