This is a Phase 1/2 study of HST-1011, a CBL-B inhibitor, being developed for the
treatment of patients with advanced solid tumors, who relapsed while on or are refractory
to approved anti-PD(L)1 therapies or other standard of care.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05662397.
Locations matching your search criteria
United States
Pennsylvania
Pittsburgh
University of Pittsburgh Cancer Institute (UPCI)Status: Active
Name Not Available
This is a Phase 1/2 study of HST-1011, a CBL-B inhibitor, being developed for the
treatment of patients with advanced solid tumors, who relapsed while on or are refractory
to approved anti-PD(L)1 therapies or other standard of care.
In Phase 1 patients will receive HST-1011 as either monotherapy (Parts A1 and A2) or in
combination with the anti-PD1 antibody, cemiplimab (Part B1 and B2).
Part A1 is a monotherapy dose escalation in which cohorts of patients will receive
increasing doses of HST-1011. Upon completion of Part A1 dose escalation, an HST-1011
monotherapy dose optimization will commence (Part A2).
Part B1 is a dose escalation of HST-1011 given in combination with the standard
dose/regimen of cemiplimab. Dosing in Part B1 may commence prior to the completion of
Part A1. Upon completion of Part B1 dose escalation, an HST-1011 dose optimization in
combination with cemiplimab will commence (Part B2).
Phase 2 will evaluate the preliminary antitumor activity of HST-1011 in combination with
anti-PD(L)1 antibody or other standard of care therapies.
Lead OrganizationHotSpot Therapeutics, Inc