This first-in-human, open-label, multicenter, multi-arm dose-escalation study is designed
to evaluate the safety, PK, and PD of ADU-1805, an anti- SIRPα monoclonal antibody, as
monotherapy and in combination with pembrolizumab (anti-PD-1 antibody).
Additional locations may be listed on ClinicalTrials.gov for NCT05856981.
Locations matching your search criteria
United States
Missouri
Saint Louis
Siteman Cancer Center at Washington UniversityStatus: Active
Name Not Available
The study will start with the ADU-1805 monotherapy dose escalation arm following an i3+3
design until the RP2D is defined. The ADU-1805 plus pembrolizumab dose escalation arm,
also following an i3+3 design, will start after clearance of the ADU-1805 monotherapy
dose level achieving maximum target engagement (e.g. ≥ 90% target engagement) and will
continue until the RP2D for the combination is defined.
Lead OrganizationSairopa B.V.