Literature DB >> 31172358

"Development of Fixed Dose Combination Products" Workshop Report: Considerations of Gastrointestinal Physiology and Overall Development Strategy.

Bart Hens1, Maura Corsetti2,3, Marival Bermejo4, Raimar Löbenberg5, Pablo M González6, Amitava Mitra7, Divyakant Desai8, Dakshina Murthy Chilukuri9, Alexis Aceituno10.   

Abstract

The gastrointestinal (GI) tract is one of the most popular and used routes of drug product administration due to the convenience for better patient compliance and reduced costs to the patient compared to other routes. However, its complex nature poses a great challenge for formulation scientists when developing more complex dosage forms such as those combining two or more drugs. Fixed dose combination (FDC) products are two or more single active ingredients combined in a single dosage form. This formulation strategy represents a novel formulation which is as safe and effective compared to every mono-product separately. A complex drug product, to be dosed through a complex route, requires judicious considerations for formulation development. Additionally, it represents a challenge from a regulatory perspective at the time of demonstrating bioequivalence (BE) for generic versions of such drug products. This report gives the reader a summary of a 2-day short course that took place on the third and fourth of November at the Annual Association of Pharmaceutical Scientists (AAPS) meeting in 2018 at Washington, D.C. This manuscript will offer a comprehensive view of the most influential aspects of the GI physiology on the absorption of drugs and current techniques to help understand the fate of orally ingested drug products in the complex environment represented by the GI tract. Through case studies on FDC product development and regulatory issues, this manuscript will provide a great opportunity for readers to explore avenues for successfully developing FDC products and their generic versions.

Entities:  

Keywords:  bioequivalence; fixed dose combination drug products; formulation prediction; gastrointestinal physiology; in vivo predictions

Mesh:

Substances:

Year:  2019        PMID: 31172358     DOI: 10.1208/s12248-019-0346-6

Source DB:  PubMed          Journal:  AAPS J        ISSN: 1550-7416            Impact factor:   4.009


  78 in total

Review 1.  Challenges and opportunities in achieving bioequivalence for fixed-dose combination products.

Authors:  Amitava Mitra; Yunhui Wu
Journal:  AAPS J       Date:  2012-06-09       Impact factor: 4.009

2.  In vitro-in situ permeability and dissolution of fexofenadine with kinetic modeling in the presence of sodium dodecyl sulfate.

Authors:  Evren Gundogdu; V Mangas-Sanjuan; Isabel Gonzalez-Alvarez; Marival Bermejo; Ercument Karasulu
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2011-08-11       Impact factor: 2.441

3.  The secretory component of the interdigestive migrating motor complex in man.

Authors:  G R Vantrappen; T L Peeters; J Janssens
Journal:  Scand J Gastroenterol       Date:  1979       Impact factor: 2.423

4.  Individualized in vitro and in silico methods for predicting in vivo performance of enteric-coated tablets containing a narrow therapeutic index drug.

Authors:  Frank Karkossa; Sandra Klein
Journal:  Eur J Pharm Biopharm       Date:  2018-12-05       Impact factor: 5.571

5.  Ambulatory assessment of colonic motility using the electromagnetic capsule tracking system.

Authors:  Esben Bolvig Mark; Jakob Lykke Poulsen; Anne-Mette Haase; Marie Espersen; Tine Gregersen; Vincent Schlageter; S Mark Scott; Klaus Krogh; Asbjørn Mohr Drewes
Journal:  Neurogastroenterol Motil       Date:  2018-08-20       Impact factor: 3.598

6.  The interdigestive motor complex of normal subjects and patients with bacterial overgrowth of the small intestine.

Authors:  G Vantrappen; J Janssens; J Hellemans; Y Ghoos
Journal:  J Clin Invest       Date:  1977-06       Impact factor: 14.808

Review 7.  The migrating motor complex: control mechanisms and its role in health and disease.

Authors:  Eveline Deloose; Pieter Janssen; Inge Depoortere; Jan Tack
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2012-03-27       Impact factor: 46.802

Review 8.  Physiological parameters for oral delivery and in vitro testing.

Authors:  Deanna M Mudie; Gordon L Amidon; Gregory E Amidon
Journal:  Mol Pharm       Date:  2010-09-07       Impact factor: 4.939

9.  Experimental studies on the influence of surfactants on intestinal absorption of drugs. Cefadroxil as model drug and sodium taurocholate as natural model surfactant: studies in rat colon and in rat duodenum.

Authors:  G Carmona-Ibáñez; M del Val Bermejo-Sanz; F Rius-Alarcó; A Martín-Villodre
Journal:  Arzneimittelforschung       Date:  1999-01

10.  Dose Determination for a Fixed-Dose Drug Combination: A Phase II Randomized Controlled Trial for Tiotropium/Olodaterol Versus Tiotropium in Patients with COPD.

Authors:  François Maltais; Alan Hamilton; Florian Voß; M Reza Maleki-Yazdi
Journal:  Adv Ther       Date:  2019-03-06       Impact factor: 3.845

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  1 in total

1.  A chromatographic approach to development of 5-aminosalicylate/folic acid fixed-dose combinations for treatment of Crohn's disease and ulcerative colitis.

Authors:  Mario-Livio Jeličić; Edvin Brusač; Daniela Amidžić Klarić; Biljana Nigović; Nikša Turk; Ana Mornar
Journal:  Sci Rep       Date:  2020-11-30       Impact factor: 4.379

  1 in total

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