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Petrides, Petro E.; Schörgenhofer, Christian; Widmann, Rudolf; Jilma, Bernd und Klade, Christoph S. (2018): Pharmacokinetics of a Novel Anagrelide Extended-Release Formulation in Healthy Subjects: Food Intake and Comparison With a Reference Product. In: Clinical Pharmacology in Drug Development, Bd. 7, Nr. 2: S. 123-131

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Abstract

Anagrelide is an established therapy for essential thrombocythemia. Common adverse effects have been linked to peak plasma concentrations of anagrelide and its 3OH metabolite. Our study was performed to investigate the pharmacokinetics (PK) of a novel anagrelide extended-release (AER) formulation and its active metabolites. Thirty healthy volunteers were randomized to receive either 2 mg AER (under fasting and fed conditions) or 2 mg commercially available reference product (CARP) in an open-label, 3-way crossover trial with washout periods of 6 days. Plasma concentrations of anagrelide and its active metabolites were assessed by tandem mass spectrometry. The PK differed significantly between all treatment periods. Bioavailability of AER was 55% of the CARP under fasting conditions and 60% under fed conditions. C-max, AUCt, and AUC infinity were significantly higher and T-max and T-1/2 were significantly shorter after the CARP compared with AER. Food had a significant impact on the PK of AER, increasing the C-max and AUC(t) while reducing the T-1/2, plateau, and mean residence time. Both formulations were well tolerated, with a trend toward more frequently occurring adverse events after the CARP. The PK of AER and the CARP differed significantly in all parameters. Food enhanced the bioavailability of AER.

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