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Originally developed by a research team at Washington State University in the United States, Dihexa is classified as an Angiotensin IV analog, yet it possesses a significantly more potent capacity for synaptogenesis (the formation of new synapses)

Health concerns such as chronic infections, metabolic issues, or autoimmune conditions can further reduce glutathione production

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The pharma is currently seeking further clarification for the rejection, with an eye toward quickly addressing the FDAs comments, according to its news release