Elsevier

Clinical Therapeutics

Volume 38, Issue 10, October 2016, Pages 2227-2238.e4
Clinical Therapeutics

Single- and Multiple-dose Pharmacokinetics of a Lorcaserin Extended-release Tablet

https://doi.org/10.1016/j.clinthera.2016.08.016Get rights and content
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open access

Abstract

Purpose

Lorcaserin is a serotonin 2C receptor agonist indicated for chronic weight management as an adjunct to diet and exercise. The initial approved formulation is a 10-mg, immediate-release (IR) tablet for administration BID. These studies investigated the single- and multiple-dose pharmacokinetic properties of a new, recently US Food and Drug Administration–approved, extended-release, 20-mg once-daily formulation.

Methods

We performed 2 separate 2-period, 2-sequence crossover studies in 36 healthy adults: a study comparing the IR formulation to the extended-release formulation under fasting conditions and a study comparing the extended-release formulation under fed and fasted conditions.

Findings

Compared with lorcaserin IR, the Tmax after a single dose of lorcaserin extended-release was greater (median, 12 vs 3 hours), and the Cmax was 26% lower (38.8 vs 52.3 ng/mL). AUC data were bioequivalent for the 2 formulations in both single- and multiple-dose regimens, confirming no formulation effect on lorcaserin bioavailability. In fasted and fed conditions, Tmax after a single dose was identical (median, 12 hours), but Cmax was approximately 45% higher in the fed state (mean, 38.5 ng/mL fasted vs 56.1 ng/mL fed). However, at steady state, Cmax and AUC were determined to be bioequivalent between the fasted and fed states, indicating no clinically relevant food effect on the pharmacokinetic properties of lorcaserin extended-release. The safety profile was consistent between the 2 formulations.

Implications

Overall, the results indicate that lorcaserin extended-release is a suitable once-daily alternative to the approved IR BID formulation.

Key words

extended-release
lorcaserin
obesity
overweight
pharmacokinetic properties

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