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To conduct PK study of CaPre
November 11, 2013
By: Gil Roth
Acasti Pharma, a subsidiary of Neptune Technologies & Bioresources Inc., has submitted an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) to initiate a Pharmacokinetic trial of CaPre in the U.S. It is an open-label, randomized, multiple-dose, single-center, parallel-design study that will evaluate blood profiles and bioavailability of omega-3 phospholipids on healthy volunteers taking single and multiple daily oral doses of 1, 2 and 4 grams of CaPre.
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