This is a phase I dose escalation study of CAN-2409 plus prodrug in patients with
non-small cell lung cancer (NSCLC). The primary clinical objective of the study is to
evaluate the safety of CAN-2409 plus prodrug when combined with standard surgery for
NSCLC. The primary scientific objective is to determine the immunologic changes induced
by CAN-2409 plus prodrug.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03131037.
Locations matching your search criteria
United States
Pennsylvania
Philadelphia
Children's Hospital of PhiladelphiaStatus: Active
Name Not Available
The purpose of this open-label, dose escalation clinical trial is to investigate the
safety of CAN-2409 (aglatimagene besadenovec) plus prodrug prior to surgery in patients
with NSCLC. CAN-2409 is a viral immunotherapy approach which utilizes intratumoral
administration to selectively induce tumor cell death and elicit both an innate and an
adaptive systemic anti-tumor immune response against the injected tumor and uninjected
metastases. Local delivery enables these effects while aiming to minimize systemic
toxicity. Standard of care surgical resection will be performed about 3 weeks after the
CAN-2409 injection. Chemotherapy and/or radiation may begin 6-8 weeks after resection
surgery. Choice of chemotherapy depends on the treating oncologist. CAN-2409
(aglatimagene besadenovec) was previously known as AdV-tk, and the combination of
CAN-2409 plus prodrug was previously known as GMCI.
Lead OrganizationCandel Therapeutics, Inc.