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As with other incretin-based agents, these events were generally more common than with placebo and were often dose-related , particularly during the dose-escalation phase of treatment

The ATP7B gene is responsible for controlling the transport of copper from intracellular proteins into secretory pathways for excretion into bile and synthesis of ceruloplasmin (a protein that binds copper in the bloodstream)[7]

99 % purity without an attached chromatogram is a claim, not proof