IMCnyeso is a bispecific fusion protein designed for the treatment of cancers that
express NY-ESO-1 and/or LAGE-1A. This was a first-in-human trial designed to evaluate the
safety and efficacy of IMCnyeso in HLA-A*02:01-positive adult participants whose cancer
is positive for NY-ESO-1 and/or LAGE-A1.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03515551.
Locations matching your search criteria
United States
Pennsylvania
Pittsburgh
University of Pittsburgh Cancer Institute (UPCI)Status: Active
Name Not Available
This was planned to be a multi-center, open label, dose finding Phase 1/2 study of single
agent IMCnyeso administered in participants with NY-ESO-1 and/or LAGE-A1 positive tumors.
The primary objective of the dose escalation phase (Phase 1) was to determine the maximum
tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of IMCnyeso in participants
with advanced solid tumors. Preliminary efficacy was to be evaluated in Phase 2. The
study was terminated early (prior to initiation of Phase 2) by the Sponsor as a strategic
decision (not based on any safety signal).
Lead OrganizationImmunocore Limited