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AG3147C UL RFT for the Provision of a Preclinical Bioavailability Study for a Drug Nanoparticle Formulation

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Description

Our objective is to conduct a study in animals that compares the pharmacokinetics of 2 oral formulations of the same drug or active pharmaceutical ingredient (API). One of the oral formulations is developed inhouse (Nanocomp), and the other is a formulation currently available in the market (Commercial). The question we intend to answer using standard pharmacokinetic analysis is: would the novel oral formulation be superior to the available formulation?

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