TY - JOUR
T1 - The Imperial College Cambridge Manchester (ICCAM) platform study: An experimental medicine platform for evaluating new drugs for relapse prevention in addiction.
T2 - Part A: Study description
AU - Paterson, Louise
AU - Flechais, Remy
AU - Murphy, Anna
AU - Reed, Laurence
AU - Abbott, Sanja
AU - Boyapati, Venkataramana
AU - Elliott, Rebecca
AU - Erritzoe, David
AU - Ersche, Karen D.
AU - Faluyi, Yetunde
AU - Faravelli, Luca
AU - Fernandez-Egea, Emilio
AU - Kalk, Nicola J.
AU - Kuchibatla, Shankar
AU - McGonigle, John
AU - Metastasio, Antonio
AU - Mick, Inge
AU - Nestor, Liam J.
AU - Orban, Csaba
AU - Passetti, Filippo
AU - Rabiner, Eugenii A.
AU - Smith, Dana
AU - Suckling, John
AU - Tait, Roger
AU - Taylor, Eleanor
AU - Waldman, Adam D.
AU - Robbins, Trevor W.
AU - Deakin, J. F. William
AU - Nutt, David J.
AU - Lingford-Hughes, Anne
N1 - cited By 10
PY - 2015
Y1 - 2015
N2 - 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.
AB - 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.
KW - Addiction
KW - Functional magnetic resonance imaging
KW - µ-Opioid receptor
KW - Neurokinin 1 receptor
KW - Dopamine D3 receptor
UR - http://journals.sagepub.com/home/jop
U2 - 10.1177/0269881115596155
DO - 10.1177/0269881115596155
M3 - Article
VL - 29
SP - 943
EP - 960
JO - Journal of Psychopharmacology
JF - Journal of Psychopharmacology
SN - 0269-8811
IS - 9
ER -