The Imperial College Cambridge Manchester (ICCAM) platform study: An experimental medicine platform for evaluating new drugs for relapse prevention in addiction. Part A: Study description

Author:

Paterson Louise M1,Flechais Remy SA1,Murphy Anna2,Reed Laurence J1,Abbott Sanja3,Boyapati Venkataramana2,Elliott Rebecca2,Erritzoe David1,Ersche Karen D34,Faluyi Yetunde5,Faravelli Luca1,Fernandez-Egea Emilio35,Kalk Nicola J1,Kuchibatla Shankar S2,McGonigle John1,Metastasio Antonio26,Mick Inge1,Nestor Liam17,Orban Csaba1,Passetti Filippo134,Rabiner Eugenii A8,Smith Dana G39,Suckling John35,Tait Roger3,Taylor Eleanor M2,Waldman Adam D10,Robbins Trevor W39,Deakin JF William2,Nutt David J1,Lingford-Hughes Anne R1,

Affiliation:

1. Centre for Neuropsychopharmacology, Imperial College London, London, UK

2. Neuroscience and Psychiatry Unit, University of Manchester, Manchester, UK

3. Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, UK

4. Department of Psychiatry, University of Cambridge, Cambridge, UK

5. Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK

6. 5 Boroughs Partnership NHS Foundation Trust, Warrington, UK

7. Clinical Research Unit, GlaxoSmithKline, Cambridge, UK

8. Imanova Ltd, London, UK

9. Department of Psychology, University of Cambridge, Cambridge, UK

10. Centre for Neuroinflammation and Neurodegeneration, Imperial College London, London, UK

Abstract

Drug and alcohol dependence are global problems with substantial societal costs. There are few treatments for relapse prevention and therefore a pressing need for further study of brain mechanisms underpinning relapse circuitry. The Imperial College Cambridge Manchester (ICCAM) platform study is an experimental medicine approach to this problem: using functional magnetic resonance imaging (fMRI) techniques and selective pharmacological tools, it aims to explore the neuropharmacology of putative relapse pathways in cocaine, alcohol, opiate dependent, and healthy individuals to inform future drug development. Addiction studies typically involve small samples because of recruitment difficulties and attrition. We established the platform in three centres to assess the feasibility of a multisite approach to address these issues. Pharmacological modulation of reward, impulsivity and emotional reactivity were investigated in a monetary incentive delay task, an inhibitory control task, and an evocative images task, using selective antagonists for µ-opioid, dopamine D3 receptor (DRD3) and neurokinin 1 (NK1) receptors (naltrexone, GSK598809, vofopitant/aprepitant), in a placebo-controlled, randomised, crossover design. In two years, 609 scans were performed, with 155 individuals scanned at baseline. Attrition was low and the majority of individuals were sufficiently motivated to complete all five sessions ( n=87). We describe herein the study design, main aims, recruitment numbers, sample characteristics, and explain the test hypotheses and anticipated study outputs.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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