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ABSTRACT: Background
To evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of eftilagimod alpha (efti), a soluble lymphocyte activation gene-3 protein, in combination with the programmed cell death-1 (PD-1) antagonist pembrolizumab.Methods
The study was divided into two parts; parts A and B, where part A was the dose escalation part and part B was an extension part of the study. Patients with metastatic melanoma were treated with efti plus the standard dose of pembrolizumab. Blood samples were assayed to determine plasma pharmacokinetic parameters, detect efti antibody formation and determine long-lived CD8 T cell responses and associated pharmacodynamic parameters.Results
Twenty-four patients with melanoma received pembrolizumab and bi-weekly subcutaneo
SUBMITTER: Atkinson V
PROVIDER: S-EPMC7682474 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature