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A randomized, double-blind, positive-controlled, prospective, dose-response clinical study to evaluate the efficacy and tolerability of an aqueous extract of Terminalia bellerica in lowering uric acid and creatinine levels in chronic kidney disease subjects with hyperuricemia
This is not the traditional way that the FDA goes about doing stuff, they typically go through phase one trials, phase two trials, phase three trials, and that takes years, says Dr
Scientific Reports, 15 (1), 1-11
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