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A Phase 1 Pharmacokinetic Study of Cysteamine Bitartrate Delayed-Release Capsules Following Oral Administration with Orange Juice,Water, or Omeprazole in Cystinosis
Authors:Danielle Armas  Robert J Holt  Nils F Confer  Gregg C Checani  Mohammad Obaidi  Yuli Xie  Meg Brannagan
Institution:1.Celerion Inc.,Phoenix,USA;2.Horizon Pharma, Inc.,Lake Forest,USA;3.College of Pharmacy,University of Illinois-Chicago,Chicago,USA;4.Clinical Pharmacology and Pharmacometrics,Celerion Inc.,Lincoln,USA;5.Celerion Inc.,Lincoln,USA
Abstract:

Introduction

Cystinosis is a rare, metabolic, autosomal recessive, genetic lysosomal storage disorder characterized by an accumulation of cystine in various organs and tissues. Cysteamine bitartrate (CB) is a cystine-depleting aminothiol agent approved in the United States and Europe in immediate-release and delayed-release (DR) formulations for the treatment of nephropathic cystinosis in children and adults. It is recommended that CBDR be administered with fruit juice (except grapefruit juice) for maximum absorption. Omeprazole is a proton pump inhibitor that inhibits gastric acid secretion and, theoretically, may cause the premature release of cysteamine by increasing intragastric pH, thereby affecting the PK of CBDR.

Methods

This open-label, three-period, randomized study in healthy adult subjects was designed primarily to compare the pharmacokinetics of CBDR capsules after a single oral dose administered with orange juice, water, or multiple oral doses of omeprazole with water at steady state. A total of 32 subjects were randomly assigned to receive study agents in one of two treatment sequences.

Results

All subjects completed the study and baseline characteristics of the overall population and the two treatment sequence populations were similar. Peak mean plasma cysteamine concentrations following co-administration of CBDR capsules with orange juice (1892 ng/mL) were higher compared with co-administration with water (1663 ng/mL) or omeprazole 20 mg and water (1712 ng/mL). Mean time to peak plasma concentration was shorter with omeprazole co-administration (2.5 h) compared with orange juice (3.5 h) or water (3.0 h). Statistical comparisons between treatment groups indicated that exposure as assessed by AUC0–t, AUC0–, and Cmax were all within the 80–125% bioequivalence ranges for all comparisons. All treatments were generally well tolerated.

Conclusion

Overall, the pharmacokinetics of cysteamine bitartrate DR capsules are not significantly impacted by co-administration with orange juice, water only, or omeprazole (with water).

Funding

Horizon Pharma, Inc.
Keywords:
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