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It is the first triple-hormone-receptor agonist to reach advanced clinical trials, activating three distinct metabolic pathways that individually would each justify their own drug development program
All authors contributed to the discussions and data interpretation that were used to form the review contained in this paper and provided input to the manuscript and approved its final version
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As noted in the prior sections, domperidone, a selective D2/D3 antagonist, also increases prolactin and alters phagocytic and oxidative burst activity in rodent macrophages (Carvalho-Freitas et al., 2008, 2011)
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