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Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Levocetirizine Dihydrochloride.
Charoo, Naseem A; Abdallah, Daud B; Ahmed, Daoud T; Abrahamsson, Bertil; Cristofoletti, Rodrigo; Langguth, Peter; Mehta, Mehul; Parr, Alan; Polli, James E; Shah, Vinod P; Kambayashi, Atsushi; Dressman, Jennifer.
Afiliación
  • Charoo NA; Adcan Pharma LLC, Industrial City of Abu Dhabi, United Arab Emirates.
  • Abdallah DB; Department of Pharmaceutics, Faculty of Pharmacy, Al Ribat University, Khartoum, Sudan.
  • Ahmed DT; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Omdurman Islamic University, Khartoum, Sudan.
  • Abrahamsson B; Oral Product Development, Pharmaceutical Technology & Development, Operations AstraZeneca, Gothenburg, Sweden.
  • Cristofoletti R; Center for Pharmacometrics & Systems Pharmacology, Department of Pharmaceutics, University of Florida, Orlando, FL, USA.
  • Langguth P; Department of Pharmaceutical Technology and Biopharmaceutics, Johannes Gutenberg University, Mainz, Germany.
  • Mehta M; United States Food and Drug Administration, Center for Drug Evaluation and Research, Silver Spring, MD, USA.
  • Parr A; Bioceutics LCC, Raleigh-Durham, NC, USA.
  • Polli JE; Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD, USA.
  • Shah VP; International Pharmaceutical Federation (FIP), The Hague, the Netherlands.
  • Kambayashi A; Pharmaceutical Research and Technology Labs, Astellas Pharma Inc, Analytical Research Laboratories, Yaizu, Japan.
  • Dressman J; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Frankfurt am Main, Germany. Electronic address: jdressman@em.uni-frankfurt.de.
J Pharm Sci ; 112(4): 893-903, 2023 04.
Article en En | MEDLINE | ID: mdl-36581104
ABSTRACT
Levocetirizine, a histamine H1-receptor antagonist, is prescribed to treat uncomplicated skin rashes associated with chronic idiopathic urticaria as well as the symptoms of both seasonal and continual allergic rhinitis. In this monograph, the practicality of using Biopharmaceutics Classification System (BCS) based methodologies as a substitute for pharmacokinetic studies in human volunteers to appraise the bioequivalence of immediate-release (IR) oral, solid dosage forms containing levocetirizine dihydrochloride was investigated, using data from the literature and in-house testing. Levocetirizine's solubility and permeability properties, as well as its dissolution from commercial products, its therapeutic uses, therapeutic index, pharmacokinetics and pharmacodynamic traits, were reviewed in accordance with the BCS, along with any reports in the literature about failure to meet bioequivalence (BE) requirements, bioavailability issues, drug-excipient interactions as well as other relevant information. The data presented in this monograph unequivocally point to classification of levocetirizine in BCS Class 1. For products that are somewhat supra-equivalent or somewhat sub-equivalent, clinical risks are expected to be insignificant in light of levocetirizine's wide therapeutic index and unlikelihood of severe adverse effects. After careful consideration of all the information available, it was concluded that the BCS-based biowaiver can be implemented for products which contain levocetirizine dihydrochloride, provided (a) the test product comprises excipients that are typically found in IR oral, solid drug products that have been approved by a country belonging to or associated with ICH and are used in quantities that are typical for such products, (b) data supporting the BCS-based biowaiver are gathered using ICH-recommended methods, and (c) all in vitro dissolution requirements specified in the ICH guidance are met by both the test and comparator products (in this case, the comparator is the innovator product).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biofarmacia / Cetirizina Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: J Pharm Sci Año: 2023 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biofarmacia / Cetirizina Tipo de estudio: Guideline Límite: Humans Idioma: En Revista: J Pharm Sci Año: 2023 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos
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