Vehicle Systems and Excipients Used in Minipig Drug Development Studies

Author:

Weaver Margaret L.1,Grossi Anette Blak2,Schützsack Jorgen3,Parish Joanna4,Løgsted Jeanet5,Bøgh Ingrid Brück6,Cameron David7,Harvey Warren8,Festag Matthias9,Downes Noel10,Venturella Silvana11,Schlichtiger Julia12,Mhedhbi Sofiene13,Ross Vanessa14,Kissner Thomas15,Stark Claudia16,Milano Stephane17,Heining Peter18,Sanchez-Felix Manual1

Affiliation:

1. Novartis Institutes for BioMedical Research, Cambridge, Massachusetts, USA

2. Ellegaard Göttingen Minipigs A/S, Dalmose, Denmark

3. LEO Pharma A/S, Ballerup, Denmark

4. Covance Laboratories Limited, Harrogate, UK

5. CiToxLAB, Scantox A/S, Lille Skensved, Denmark

6. Novo Nordisk A/S, Gentofte, Denmark

7. Huntingdon Life Sciences, Cambridgeshire, UK

8. Charles River Laboratories, Edinburgh, UK

9. F Hoffman-La Roche Ltd, Roche Innovation Center, Basel, Switzerland

10. Sequani Limited, Herefordshire, UK

11. Research Toxicology Centre S.p.A., Pomezia, Italy

12. Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany

13. Galderma Research & Development, Biot, France (current address Villeneuve Loubet, France)

14. Huntingdon Life Sciences, Huntingdon, Cambridgeshire, UK

15. Sanofi-Aventis Deutschland GmbH, Frankfurt, Germany

16. Bayer HealthCare, Berlin, Germany

17. WIL Research Europe BV, Lyon, France

18. Novartis Institutes for BioMedical Research, Basel, Switzerland

Abstract

Minipigs have been used for dermal drug development studies for decades, and they are currently more frequently considered as the second nonrodent species for pivotal nonclinical studies, in lieu of the dog or nonhuman primate, for compounds delivered via standard systemic routes of administration. Little is known about the tolerability of different excipients in minipigs; sharing knowledge of excipient tolerability and compositions previously used in nonclinical studies may avoid testing of inadequate formulations, thereby contributing to reduced animal usage. This article reviews vehicles employed in the Göttingen® minipig based on the combined experience from a number of pharmaceutical companies and contract research organizations. The review includes vehicles tolerated for single or multiple dosing by the Göttingen minipig, some of which are not appropriate for administration to other common nonrodent species (e.g., dogs). By presenting these data for dermal, oral, subcutaneous, and intravenous routes of administration, studies to qualify these vehicles in minipigs can be minimized or avoided. Additionally, investigators may more frequently consider using the minipig in place of higher species if the tolerability of a vehicle in the minipig is known.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

Reference18 articles.

1. Discovery Formulations: Approaches and Practices in Early Preclinical Development

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