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Development of a Once-Daily Modified-Release Formulation for the Short Half-Life RIPK1 Inhibitor GSK2982772 using DiffCORE Technology.
Tompson, Debra; Whitaker, Mark; Pan, Rennan; Johnson, Geoffrey; Fuller, Teresa; Zann, Vanessa; McKenzie, Litza; Abbott-Banner, Kathy; Hawkins, Simon; Powell, Marcy.
Afiliação
  • Tompson D; Clinical Pharmacology Modelling and Simulation, Medicines Research Centre, GlaxoSmithKline, Gunnels Wood Road, Stevenage, SG1 2NY, Hertfordshire, UK. debra.j.tompson@gsk.com.
  • Whitaker M; Medicine Process Delivery, GlaxoSmithKline, Dave Jack Medicines Development Centre, Park Road, SG12 0DP, Hertfordshire, UK.
  • Pan R; Pharmaceutical Development, GlaxoSmithKline, 1250 S. Collegeville Road, Collegeville, Pennsylvania, 19426, USA.
  • Johnson G; Development Biostatistics, GlaxoSmithKline, 1250 S. Collegeville Road, Pennsylvania, 19426, Collegeville, USA.
  • Fuller T; Global Clinical Sciences and Delivery, Medicines Research Centre, GlaxoSmithKline, Gunnels Wood Road, Stevenage, SG1 2NY, Hertfordshire, UK.
  • Zann V; Quotient Sciences Limited, Mere Way, Ruddington, NG11 6JS, Nottingham, UK.
  • McKenzie L; Quotient Sciences Limited, Mere Way, Ruddington, NG11 6JS, Nottingham, UK.
  • Abbott-Banner K; Discovery Medicine, GlaxoSmithKline, 980 Great West Road, Brentford, TW8 9GS, Middlesex, UK.
  • Hawkins S; Discovery Medicine, GlaxoSmithKline, 980 Great West Road, Brentford, TW8 9GS, Middlesex, UK.
  • Powell M; Safety and Medical Governance, GlaxoSmithKline, 5 Moore Drive, Research Triangle Park, North Carolina, 27709-3398, USA.
Pharm Res ; 39(1): 153-165, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34988780
PURPOSE: GSK2982772 is a selective inhibitor of receptor-interacting protein kinase-1 (RIPK1) with a short 2- to 3-h half-life. In a previous modified-release (MR) study, a matrix monolithic formulation (80% GSK2982772 released over 12 h) provided a once-daily (QD) pharmacokinetic (PK) profile in the fasted state; however, it was susceptible to food effects. The current study evaluated the safety and PK of MR formulations using GSK proprietary DiffCORE™ technology. METHODS: Part A evaluated PK following single-dose (240 mg) fasted and fed (high-fat meal) administration of three DiffCORE MR formulations within pre-defined in vitro extremes of 80% GSK2982772 released over 12 h (MR-12 h) to 80% GSK2982772 released over 18 h (MR-18 h) versus an immediate-release formulation. Part B evaluated MR-16 h (120-960 mg) in different prandial states. RESULTS: Pharmacokinetic profiles for all MR formulations and doses tested in the fasted and fed states were consistent with QD dosing. CONCLUSIONS: The DiffCORE technology overcame the food effect vulnerability observed with the matrix monolithic formulation. The MR-16 h formulation was selected for further clinical development as a QD dosing regimen (NCT03649412 September 26, 2018).
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Oxazepinas Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Pharm Res Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Oxazepinas Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Pharm Res Ano de publicação: 2022 Tipo de documento: Article