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Resveratrol and hydroxypropyl--cyclodextrin (HP--CD) showed great superiority in pharmacokinetic profile compared to the resveratrol and starch mixture in a human study, demonstrating 4.8 higher resveratrol Cmax, a shorter Tmax and t1/2, and better absorption extent and rate [202]

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Market launch would follow 13 months after approval, placing patient access at Q1Q2 2028

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