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Clinical Trial Summary

Study will define the bioavailability and short term pharmacokinetics of the principal secondary metabolites of a aqueous-ethanolic extract of H. procumbens in non-enteric and enteric capsules.


Clinical Trial Description

The study(n = 12) will use a one-dose design to measure bioavailability and pharmacokinetic properties of an aqueous extract of H. procumbens containing 100mg harpagoside. Plasma levels of harpagoside, harpagide, verbascoside, and 8-p-coumarylharpagide will be measured for 24 hours with blood collections taken at timed intervals. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03641248
Study type Interventional
Source University of Missouri-Columbia
Contact
Status Withdrawn
Phase Early Phase 1
Start date May 1, 2021
Completion date August 31, 2021

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