This is an open-label, non-randomized, multicenter, Phase 1/2a study to evaluate the safety and potential efficacy of Allocetra-OTS in the treatment of advanced solid tumor malignancy as monotherapy or in combination with an anti-PD-1 therapy.
Despite the advent of novel targeted and immunotherapeutics for the treatment of solid tumors, many patients remain without cure. Allocetra-OTS is an immunomodulatory cell-based therapy consisting of allogeneic peripheral blood mononuclear cells that have been modified to be engulfed by macrophages and reprogram them into their homeostatic state. This is an open-label, non-randomized, multicenter, Phase 1/2a study to evaluate the safety and potential efficacy of Allocetra-OTS in the treatment of advanced solid tumor malignancy as monotherapy (Stage 1), and in combination with an anti-PD-1 therapy (Stage 2). Allocetra-OTS will be administered systemically or locally (intravenous \[IV\] or intraperitoneal \[IP\]) according to the tumor location.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
14
Allocetra-OTS is a cell-based therapy consisting of non-HLA matched allogeneic peripheral blood mononuclear cells, derived from a healthy human donor following a leukapheresis procedure, induced to an apoptotic stable state.
Immune checkpoint inhibitor (anti-PD-1 antibody)
Immune checkpoint inhibitor (anti-PD-1 antibody)
Rambam Medical Center
Haifa, Israel
Hadassah Medical Center
Jerusalem, Israel
Sheba Medical Center
Ramat Gan, Israel
Sourasky Medical Center
Tel Aviv, Israel
Clínica Universidad de Navarra
Safety of Allocetra-OTS
Characterize the safety of Allocetra-OTS based on the dose-limiting toxicities (DLTs) of Allocetra-OTS as monotherapy or in combination with anti-PD1 therapy.
Time frame: 3-5 weeks
Overall Response Rate (ORR)/Best Overall Response Rate (BORR)
Overall Response Rate (ORR)/Best Overall Response Rate (BORR) (percentage of patients who achieve best response of complete response \[CR\] or partial response \[PR\]).
Time frame: 12 months
Clinical benefit rate (CBR)
Clinical benefit rate (CBR) (percentage of patients who achieve best response of CR, PR or stable disease \[SD\]).
Time frame: 12 months
Duration of response (DoR)
Duration of response (DoR), defined as the time from first documented evidence of CR or PR until disease progression or death.
Time frame: 12 months
Time to response (TTR)
Time to response (TTR), defined as the time to the first documented CR or PR.
Time frame: 12 months
Progression-free survival (PFS)
Progression-free survival (PFS), defined as the time to disease progression or death due to any cause.
Time frame: 12 months
Overall survival (OS)
Overall survival (OS) defined as the time to death due to any cause.
Time frame: 12 months
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Madrid, Spain
NEXT Madrid
Madrid, Spain