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Pharmacokinetics of HLD200, a Delayed-Release and Extended-Release Methylphenidate: Evaluation of Dose Proportionality, Food Effect, Multiple-Dose Modeling, and Comparative Bioavailability with Immediate-Release Methylphenidate in Healthy Adults.
Liu, Tao; Gobburu, Jogarao V S; Po, Michelle D; McLean, Angus; DeSousa, Norberto J; Sallee, Floyd R; Incledon, Bev.
Afiliación
  • Liu T; 1 Center for Translational Medicine, School of Pharmacy, University of Maryland, Baltimore, Maryland.
  • Gobburu JVS; 1 Center for Translational Medicine, School of Pharmacy, University of Maryland, Baltimore, Maryland.
  • Po MD; 2 Highland Therapeutics Inc., Toronto, Ontario, Canada.
  • McLean A; 3 Ironshore Pharmaceuticals and Development, Inc., Camana Bay, Cayman Islands.
  • DeSousa NJ; 3 Ironshore Pharmaceuticals and Development, Inc., Camana Bay, Cayman Islands.
  • Sallee FR; 3 Ironshore Pharmaceuticals and Development, Inc., Camana Bay, Cayman Islands.
  • Incledon B; 3 Ironshore Pharmaceuticals and Development, Inc., Camana Bay, Cayman Islands.
J Child Adolesc Psychopharmacol ; 29(3): 181-191, 2019 04.
Article en En | MEDLINE | ID: mdl-30810347
OBJECTIVES: HLD200, an oral, once-daily, evening-dosed, delayed-release, and extended-release methylphenidate (DR/ER-MPH), was designed to provide efficacy from the early morning, throughout the day, and into the evening to individuals with attention-deficit/hyperactivity disorder. The objectives were to evaluate DR/ER-MPH pharmacokinetic (PK) properties in healthy adults, including dose proportionality, food effect, the potential of accumulation using multiple-dose modeling, and bioavailability compared to an immediate-release MPH (IR MPH). METHODS: Three open-label, single-dose, crossover studies were conducted, all with a 7-day washout between treatments. In Study I, 20 subjects received evening-dosed DR/ER-MPH (20 and 100 mg) followed by a medium-fat breakfast; 13 subjects received a subsequent 100-mg dose of DR/ER-MPH followed by a low-fat breakfast. In Study II, 18 subjects were evaluated after receiving evening-dosed DR/ER-MPH (100 mg) under 3 conditions: immediately after a high-fat meal, sprinkled on applesauce, and in a fasted state. In Study III, 11 and 12 subjects received evening-dosed DR/ER-MPH (100 mg) and morning-dosed IR MPH (20 mg), respectively. RESULTS: DR/ER-MPH demonstrated dose proportionality between 20- and 100-mg doses. DR/ER-MPH PK parameters were not significantly affected by breakfast content or by sprinkling capsule contents. A high-fat meal immediately preceding evening dosing did not affect total MPH exposure but lowered peak MPH exposure by 14% and 11% versus fasted and sprinkled states, and time to peak exposure was delayed by ∼2.5 hours; these PK differences are unlikely to be clinically significant. Based on multiple-dose simulations using data from Study I, negligible accumulation of DR/ER-MPH was predicted. The relative bioavailability for DR/ER-MPH compared to IR MPH was 73.9%. No serious adverse events (AEs) were reported, and the observed AEs were consistent with MPH. There were no discontinuations in Studies I and III, but three participants withdrew in Study II due to AEs. CONCLUSIONS: Evening-dosed DR/ER-MPH demonstrated dose proportionality and can be administered with or without food. Significant accumulation is unlikely with multiple dosing.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Preparaciones de Acción Retardada / Estimulantes del Sistema Nervioso Central / Metilfenidato Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Child Adolesc Psychopharmacol Asunto de la revista: PEDIATRIA / PSICOFARMACOLOGIA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Preparaciones de Acción Retardada / Estimulantes del Sistema Nervioso Central / Metilfenidato Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Child Adolesc Psychopharmacol Asunto de la revista: PEDIATRIA / PSICOFARMACOLOGIA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos