Pts are required to have ASPH+ SCCHN, actively receiving pembrolizumab or nivolumab for ≥12 weeks, & have a best response of stable disease (SD) or first evidence of progressive disease (PD). Funding: Sensei Biotherapeutics, Inc. Clinical trial identification: NCT04034225; July 16, 2019.
Anti-PD-1 antibodies such as pembrolizumab and nivolumab can induce durable clinical responses in 13-16% SCCHN patients. Early safety/efficacy warrant further evaluation of this combination therapy. Trial will be proceeding to full enrollment after the safety run-in is completed. Research Funding: None
over 4 years ago
Clinical • P1/2 data • PD(L)-1 Biomarker • IO biomarker