Cannabidiol as a potential treatment for anxiety disorders. Esther Blessing, MD PhD
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1 Cannabidiol as a potential treatment for anxiety disorders Esther Blessing, MD PhD
2 Overview History and of cannabidiol (CBD) and cannabis Safety and tolerability of CBD CBD pharmacology Clinical need for anxiolytic drugs Evidence for CBD as an anxiolytic Current clinical research with CBD and cannabinoid related drugs
3 What is cannabidiol? CBD is one of ~ 100 cannabinoid compounds unique to Cannabis plants CBD does not produce psychoactive effects like 9- THC, the other main cannabinoid Cannabinoids produced by trichome glands in hairs of buds on female Cannabis plants Female plants Flower buds Trichome glands Dried bud
4 Cannabis Commonly used psychoactive substance worldwide Multiple varieties varying in cannabinoid composition C. Indica C. Sativa Used for fiber Sedative CBD:THC ratio Strong high THC:CBD ratio Increasing legalization and medical use
5 History of medicinal cannabis use (1) ~ 8,000 BCE use in China as rope, later used for garments, paper, and medicine 2700 BCE Used in ancient Egypt, India, Africa, Greece, Rome and Arab world to treat multiple ailments Marijuana Tax Act- prohibited use, AMA opposed delta-9-tetrahydrocannabinol (THC) isolated by Raphael Mechoulam THC determined to be drug with no accepted use Randell gets IND to treat glaucoma in court battle
6 History of medicinal cannabis use (2) s Small randomized clinical trials for treating epilepsy s Human and animal experimental trials show low-dose THC is anxiolytic, high dose is anxiogenic and pro-psychotic Synthetic THC (eg marinol and cesamet) approved by FDA for treatment of cancer associated nausea, pain, loss of appetite 1996 CB1 receptor cloned, endocannabinoid system discovered
7 History of medicinal cannabis use (2) California legalizes Cannabis for AIDS, cancer treatment 2000s Role of the endocannabinoid system in emotional brain discovered, explosion in cannabinoid research 2010s Sativex: 50/50 THC/CBD oral spray approved for spasticity in MS in the UK 2015 Completion of Phase II trials for Epidiolex: pure CBD oral for treatment of childhood epilepsy in the US
8 Cannabidiol Plant-derived Cannabinoids ~ 100 different types in Cannabis Cannabinol Cannabigerol Tetrahydrocannabivarin Cannabichromene Izzo et al, Cell, 2009 Fo Δ 9 Tetrahydro cannabinol
9 Endocannabinoids (ecbs) (Endogenous activators of the cannabinoid receptor) ecbs: Anandamide & 2-AG Enzymes FAAH and MGL CB1 and CB2 receptors receptor Other receptors, eg TRP receptors DiMarzo 2004
10 The Cannabinoid receptors (Endogenous activators of the cannabinoid receptor)
11 Endocannabinoids (ecbs) (Endogenous activators of the cannabinoid receptor) ecbs synthesized from cell lipids in response to strong neuronal activity ecbs activate the CB1 receptor and other receptors on presynaptic GABA and glutamate neurons, leads to neurotransmitter inhibition Brain-wide and in periphery Roles in appetite, inflammation, emotion, nociception, etc
12 Endocannabinoids currently an anxiolytic drug target
13 Increasing interest in cannabidiol CBD characterized in 1963 by Raphael Mechoulam
14 Multiple clinical uses for CBD Anxiolytic / sedative s initial acute dosing studies in rat and human show anxiolytic effects, reversing effects of THC (Zuardi et al) Anti-epileptic controlled clinical trials with CBD in epilepsy, 2015 Orin Devinsky, NYU Langone, JAMA neurology, Epidiolex (pure CBD) reduces seizures in Dravet-syndrome Anti-inflammatory, anti-emetic, antineoplastic, neuroprotective, anti-diabetic Devinsky et al, Epilepsia, 2014 Campos et al, Phil Trans Lon, 2012
15 Overview Safety and tolerability of CBD CBD pharmacology Clinical need for anxiolytic drugs Evidence for CBD as an anxiolytic Current clinical research with CBD and cannabinoid related drugs
16 Safety and tolerability of CBD Well tolerated across a wide dose range, up to 1500 mg/day oral no reported psychomotor slowing, negative mood effects, or vital sign abnormalities, although some mild sedative effects (Bergamaschi, 2011). Pediatric phase III trials completed, (Devinsky et al, 2015) Drug-drug interactions: potent inhibitor of P450 isozymes, primarily CYP2C and CYP3A classes may potentiate THC effects when given in combination
17 CBD pharmacology (1) *Indirect effects Campos et al, 2012; McPartland et al, 2015; Ibeas et al, 2015
18 CBD pharmacology (2) Complicated! ~ 65 targets, mostly enzymes Not clear whether in vitro receptor data represents physiological in vivo effects Disputed whether CBD acts on the endocannabinioid system Many targets remain uncharacterized McPartland et al, 2015; Ibeas et al, 2015
19 Overview Clinical need for anxiolytic drugs Evidence for CBD as an anxiolytic Current clinical research with CBD and cannabinoid related drugs
20 Anxiety disorders overview Combined US lifetime prevalence of 29 %, highest of any mental disorder, immense social and economic burden DSM-4 Trauma DSM5
21 Current anxiolytic medications Serotonin reuptake inhibitors; serotonin norepinephrine DSM-4 reuptake inhibitors; benzodiazepines; MAO inhibitors; tricyclic antidepressant drugs; partial 5-hydroxytryptamine (5-HT) 1A receptor agonists Anticonvulsants and atypical antipsychotics also used to treat PTSD Associated with limited response rates and residual symptoms, particularly in PTSD Adverse effects limit tolerability and adherence
22 Barriers to drug development 3-12 billion to the development of new agents, including failure costs Unclear pipelines: preclinical anxiety tests lack not only predictive validity (the ability to predict new drugs) but also postdictive validity (sensitivity to existing drugs). Forbes.com: The truly staggering cost of investing new drugs
23 Overview Evidence for CBD as an anxiolytic Current clinical research with CBD and cannabinoid related drugs
24 Converging evidence for CBD as an anxiolytic 1. Epidemiologic 2. Preclinical (animal model) evidence 3. Role for endocannabinoids in anxiety 4. Human experimental data Cannabidiol as a Potential Treatment for Anxiety Disorders Blessing EM, Steenkamp MM, Manzanares J, Marmar CR Neurotherapeutics, 2015
25 Epidemiological evidence Limited: Reports marijuana with higher CBD:THC ratio reduces risk of psychosis (Manseau et al, 2015; Iseger et al, 2015) Anecdotal evidence that smoking marijuana reduces anxiety, but anxiogenic effects also reported, complex causal interactions possible, requires further controlled studies also not specific for CBD
26 Preclinical evidence Strong: CBD reduces multiple anxiety behaviors in over 50 studies, including both unconditioned and conditioned behaviors Suggests potential for treating PTSD, GAD and PD However: U-shaped dose curve evident (maybe due to TRP channel activation), also different effective doses in different paradigms. Chronic data lacking.
27 Human experimental evidence (1) Strong psychological data: Multiple studies: CBD ( mg) reduces anxiety associated with public speaking, imaging procedure anxiety and THC ingestion in normal and SAD subjects (Zuardi) CBD may enhance extinction of conditioned fear (Das 2012) However: No dose finding studies published
28 Human experimental evidence (2) Moderate neuroimaging evidence Several small sample functional imaging studies suggest oral CBD ( mg) reduces activation in the amygdala and other brain areas associated with anxiety (Fusar-Poli et al)
29 CBD as an anxiolytic: evidence summary Moderate-strong preclinical and acute human experimental evidence to suggest broad anxiolytic effects Chronic dosing studies in clinical populations needed Unknown what the most effective anxiolytic dose, dose-finding studies needed
30 Overview Current clinical research issues with CBD and cannabinoid related drugs
31 Current landscape for CBD and anxiety Chronic dosing with dose-finding studies in clinical populations needed Stigma associated with CBD originating from a schedule I drug persist Limited sources of pure with Phase I safety data available likely to increase with changing legal landscape Stay tuned!!
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