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Encouraged by their success with the dual agonist, Tschp and DiMarchi wondered if it was possible to go a step further and develop a peptide to simultaneously target three key metabolically-related hormone receptors: GLP-1, GIP and glucagon

They also confirmed that concurrent treatment with JHU083 and anti-PD-1 checkpoint inhibitor improved the antitumor effects compared with anti-PD-1 treatment alone, suggesting the presence of metabolic plasticity between cancer cells and effector T cells, which could be exploited as a metabolic checkpoint for cancer immunotherapy 200

Hjorth, S

Individual results vary based on baseline hormone levels, health status, and adherence to treatment protocols