TY - JOUR
T1 - The Imperial College Cambridge Manchester (ICCAM) platform study
T2 - An experimental medicine platform for evaluating new drugs for relapse prevention in addiction. Part A: Study description
AU - ICCAM Platform
AU - Paterson, Louise M
AU - Flechais, Remy S A
AU - Murphy, Anna
AU - Reed, Laurence J
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 S
AU - McGonigle, John
AU - Metastasio, Antonio
AU - Mick, Inge
AU - Nestor, Liam
AU - Orban, Csaba
AU - Passetti, Filippo
AU - Rabiner, Eugenii A
AU - Smith, Dana G
AU - Suckling, John
AU - Tait, Roger
AU - Taylor, Eleanor M
AU - Waldman, Adam D
AU - Robbins, Trevor W
AU - Deakin, J F William
AU - Nutt, David J
AU - Lingford-Hughes, Anne R
N1 - © The Author(s) 2015.
PY - 2015/8
Y1 - 2015/8
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 - Adult
KW - Behavior, Addictive
KW - Biomedical Research
KW - Brain
KW - Cocaine
KW - Cross-Over Studies
KW - Drug Discovery
KW - Ethanol
KW - Female
KW - Humans
KW - Impulsive Behavior
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Naltrexone
KW - Neurokinin-1 Receptor Antagonists
KW - Pharmaceutical Preparations
KW - Receptors, Dopamine D3
KW - Receptors, Neurokinin-1
KW - Reward
KW - Secondary Prevention
KW - Substance-Related Disorders
KW - Journal Article
KW - Randomized Controlled Trial
KW - Research Support, Non-U.S. Gov't
U2 - 10.1177/0269881115596155
DO - 10.1177/0269881115596155
M3 - Article
C2 - 26246443
SN - 0269-8811
VL - 29
SP - 943
EP - 960
JO - Journal of Psychopharmacology
JF - Journal of Psychopharmacology
IS - 9
ER -