DOCSLIB.ORG

The Path Forward for Psychedelic Assisted Psychotherapy Investor Presentation July 2020 Our Mission

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
The Path Forward for Psychedelic Assisted Psychotherapy Investor Presentation July 2020 Our Mission The Path Forward for Psychedelic Assisted Psychotherapy Investor Presentation July 2020 Our Mission To bring the world to life through psychedelics and psychedelic enhanced psychotherapy. ©2020 Core One Labs 22 The Problem Mental health conditions are on the rise. Rapid Growth. Limited Treatments. ©2020 Core One Labs 3 75% Non-adherence rates to anti-depressants +2 Current treatments haven’t Point improvement on Hamilton changed in decades Depression Score (out of 52) and have proven to be ineffective with 40-71% undesired side-effects Relapse rates Side Effects Addiction, Insomnia, Agitation, Loss of Libido, Violent Impulses, Suicidal Impulses 1. Star*D Study ©2020 Core One Labs 4 Psychedelics: A Promising Solution The results from the clinical and academical studies on psychedelic-assisted psychotherapy are compelling Evidence for Psychedelic Therapies For depression For addiction For general well-being Extended relief from Addiction decreases after Sustained improvement in quality depression >3months psilocybin treatment oflife and satisfaction 75 40 Severe days First psilocybin treatment following depression week 4 assessments 30 drinking participants Mo d e r a t e 50 of depression of (%) (%) 20 (%) Mild depression 25 Percent 10 Percent Before 1 2 3 5 3 Weeks Weeks Weeks Weeks Weeks 2 months after 2 months 14 months treatment W eek Weeks Weeks Weeks Months 1-4 5-6 9-12 13-24 25-36 methylphenidate after after treatment psilocybin psilocybin (control) treatment treatment Source: Psilocybin with Psychological Support for Treatment Resistant Source: Psilocybin-assisted treatment for alcohol dependence: Source: Psilocybin-occasioned mystical-type experience in combination with Depression, R. Carhart-Harris, The Lancet A proof- ofconcept study, M. Bogenshutz, Journal of Psychopharmacology meditation [...] R. Griffiths, Journal of Psychopharmacology ©2020 Core One Labs 5 100=maximum Compared to other drugs, psychedelics have a low harm profile ©2020 Core One Labs 6 Total Market Potential $16B Anxiety Disorder $38B & Botanical Supplements Depression Treatment Market 2 Market 1 $10B Illustrative Adult Use Market 3 *Sour1Source: Global Newswire, Reports and Data, May 2019 2Source: ”Botanical Supplements Market Size and Forecast, Hexa Research September 20183Estimated at % of global cannabis market based on relative proportion of use. Global Newswire, Reports and Data, May 2019. ©2020 Core One Labs **Source: US Substance Abuse and Mental Health Administration (SAMHSA) 7 Our Strategy We are pursuing the development and commercialization of rapid onset treatments capable of improving health outcomes. Our first product is CannaStrips which we will aim to use as a delivery tool for cannabis and psychedelic treatments. We will achieve this through R&D and Clinical Trials at the University of British Columbia. We offer a fully operational Clinic in British Columbia with 8 years of operating history. The Clinic provides training and education for medical professionals interested in psychedelic assisted psychotherapy and psychedelic integration psychotherapy. Leveraging its existing SOPs, data driven research sets and practitioner education modules, we will roll out Clinics across Canada. ©2020 Core One Labs 8 How Our Solution Works: Using psychedelic molecules to catalyze the efficacy of psychotherapy is showing great promise Psychedelic Assisted Psychotherapy Treatment Sessions Integration Therapy On-Going Care Approval of the treatment plan Psychotherapists will help your patient Typical treatment is 6 dosing sessions First dosing session integrate the experiences using with 3 integration sessions. Licensed psychotherapist, immediately different clinical psychology techniques Patients will also have access to our following the dosing session, provide Drive habit change and outlook/mindset digital patient portal for on-going exploratory therapy. improvements. support and education to help sustain Dosing sessions are typically the effects of the KAP. scheduled 2-3 days apart. ©2020 Core One Labs 9 Conduct comprehensive R&D campaigns targeting the following indications: Treatment-Resistant Depression (TRD) Addiction PTSD/Brain Injury Aging/Dementia Anxiety/Obsessive-Compulsive Indications for Clinical Treatment Rollout Disorder (OCD) Offer specialty therapy as a complementary, follow-on service Naturopathic Clinician Psychologist Cognitive and Psychodynamic Psychotherapists Family Therapist Adult Psychiatrist ©2020 Core One Labs 10 Current Delivery System Edible Polymer Sublingual Strips CannaStrips™, a precisely dosed edible polymer delivery strip similar to a breath strip. Placed under the tongue CannaStrips™ deliver the active ingredient (functional mushrooms, Psilocybin THC, CBD, others) directly into circulation. Avoids imprecise dosing and first-pass metabolism in the liver inherent with ingested products. CannaStrips™ offer an effective dosage with no degradation of the liver. The result is a consistent, precise, and effective experience. Core One Labs has control of all stages of production, distribution, transportation and delivery of CannaStrips™. ©2020 Core One Labs 11 Future Treatments Psychedelic-Enhanced Psychotherapy Our therapy will use regulated dosages of psychedelic compounds like ketamine and psilocybin in a safe, fully supervised setting. The treatment will be used alongside psychotherapy. These lower doses can promote better mental health by disrupting thought patterns or loops that may be preventing progress. The experience has been described as ”euphoric,” “calming,” and “mystical.” ©2020 Core One Labs 1212 Comparables Integrated Intellectual Valuation Clinics Focus Molecule Model Property (CAD) Psilocybin, Delivery Core One Labs Yes Multi $45MM Ketamine, THC Technology Mydecine Yes Clinic Psilocybin $140MM Innovations Group MindMed No Drug Development 18-MC, LSD Phase 1, Phase 2 $145MM Psilocybin Psilocybin, Numinus Yes Multi cultivation and $30MM Ketamine extraction license Delivery Cybin Yes Multi Psilocybin $60MM Technology Champignon Yes Multi Psilocybin+CBD Pre-clinical $150MM Brands Ketamine, FT- Field Trip Yes Multi Ft-104 molecule $69MM 104 ATAI (Perception, Drug Arketamine, No Unknown $312MM DemeRx) Development Ibogaine As of Date to May 20, 2020 *estimated valuation ©2020 Core One Labs 13 Capital Structure Core One Labs 68,000,0001 Price $0.66 Market Cap $44,800,000 Cash $4,000,000 Assets $20,500,00 1. Post-acquisition of Shacor and Rejuva ©2020 Core One Labs 14 14 Thank You Core One Labs Inc 1130 Pender Street West, Suite 820 Vancouver, BC V6E 4A4 Canada +1 (866) 347-5058.
Load more

Recommended publications
  • SPRAVATO® Esketamine Hydrochloride DATA SHEET
    SPRAVATO® esketamine hydrochloride DATA SHEET 1. PRODUCT NAME SPRAVATO® esketamine hydrochloride 32.3mg (equivalent to 28mg esketamine) nasal spray 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each single use nasal spray device delivers two sprays, one spray into each nostril. Total volume of drug product per device to be delivered is 0.2 mL containing a total of 32.3 mg of esketamine hydrochloride (equivalent to 28 mg of esketamine). For the full list of excipients, see Section 6.1 List of Excipients. 3. PHARMACEUTICAL FORM Nasal spray, solution. Clear, colourless, aqueous solution. 4. CLINICAL PARTICULARS 4.1 Therapeutic Indications SPRAVATO in conjunction with an oral antidepressant, is indicated for: - treatment resistant depression (Major Depressive Disorder in adults who have not responded adequately to at least two different antidepressants of adequate dose and duration to treat the current depressive episode). - rapid reduction of depressive symptoms in patients with Major Depressive Disorder who have acute suicidal ideation or behaviour. SPRAVATO is not indicated to prevent suicide or in reducing suicidal ideation or behaviour (see section 4.4. Special Warnings And Precautions For Use) 4.2 Dose and method of administration In patients with TRD, SPRAVATO should be administered in conjunction with a newly initiated oral antidepressant (AD) therapy. In patients with MDSI, SPRAVATO should be administered in conjunction with standard of care therapy. During the Phase III MDSI clinical program, standard of care oral AD treatment (either AD monotherapy or AD plus augmentation therapy) was initiated or optimised. Important Considerations Prior to Initiating and During Therapy SPRAVATO must be administered under the direct supervision of a healthcare provider.
    [Show full text]
  • Around the Corner Canadian Equity Research Emerging Companies and Industries to Watch 3 March 2020
    Around the Corner Canadian Equity Research Emerging companies and industries to watch 3 March 2020 Tania Gonsalves, CFA | Analyst | Canaccord Genuity Corp. (Canada) | [email protected] | 1.416.996.8346 Scott McFarland | Associate | Canaccord Genuity Corp. (Canada) | [email protected] | 1.416.998.7202 Around the Corner highlights what we believe are some of the most exciting Psychedelic-derived medicines and therapies emergent private companies in Canada, and/or industry themes and trends which are yet to be fully represented in the Mental health miracle or another bad trip? public markets. When most of us think of psychedelic drugs, we think of the 1960s counterculture. We We aim to offer insight into early industry think of anti-establishment, anti-war, anti-capitalist hippies, Woodstock, tie-dye, Lucy in trends, educate investors about private the Sky, peace, love and bell bottom jeans. But before psychedelics became ingrained in companies that are making a mark, and the counterculture, they were found in a lab. The first wave of scientific research on identify companies that may enter the psychedelics took place between 1950-65. Sandoz Pharmaceutics, what is now Novartis public markets in the future. AG (NVS-NYSE), the third largest pharmaceutical company in the world, used to market We do not provide any ratings or price LSD and psilocybin for psychotherapeutic purposes. Psychedelics weren’t born of the targets, nor should any be inferred, for counterculture. They were killed by it. The proliferation of recreational use spurred any uncovered company featured in government intervention and by 1971, psilocybin, LSD, ibogaine, mescaline, peyote, Around the Corner.
    [Show full text]
  • Janssen Research & Development, LLC Advisory Committee Briefing
    Janssen Research & Development, LLC Advisory Committee Briefing Document Esketamine Nasal Spray for Patients with Treatment-resistant Depression JNJ-54135419 (esketamine) Status: Approved Date: 16 January 2019 Prepared by: Janssen Research & Development, LLC EDMS number: EDMS-ERI-171521650, 1.0 ADVISORY COMMITTEE BRIEFING MATERIALS: AVAILABLE FOR PUBLIC RELEASE 1 Status: Approved, Date: 16 January 2019 JNJ-54135419 (esketamine) Treatment-resistant Depression Advisory Committee Briefing Document GUIDE FOR REVIEWERS This briefing document provides 3 levels of review with increasing levels of detail: The Executive Overview (Section 1, starting on page 11) provides a narrative summarizing the disease, need for novel treatments, key development program characteristics for esketamine nasal spray, study results, and conclusions. References are made to the respective supporting sections in the core document. The core document (Section 2 to Section 11, starting on page 30) includes detailed summaries and discussion in support of the Executive Overview. The appendices (starting on page 180) provide additional or more detailed information to complement brief descriptions provided in sections of the core document (e.g., demographic and baseline characteristics of the study populations, additional efficacy analyses in the Phase 3 studies, statistical methods). These appendices are referenced in the core document when relevant. This review structure allows review at varying levels of detail; however, reviewers who read at multiple levels will necessarily
    [Show full text]
  • Glutamatergic Synapse: a Promising Target to Treat Major Depressive Disorder (Mdd)
    GLUTAMATERGIC SYNAPSE: A PROMISING TARGET TO TREAT MAJOR DEPRESSIVE DISORDER (MDD) Glutamatergic Synapse: A Promising Target to Treat Major Depressive Disorder (MDD) Varinder Garg1, Harish Kumar2, Surinder Rana3, Bikramjeet Singh Kalsi4, Lakshmi Akhila Rajnala5, Ramandeep Kaur6, Jyoti Rustagi7, Swati8, Chesta9 1 MBBS, MD Principal Investigator, ICMR-Centre for Innovation and Bio-Design, Room No. 2022 and 2027, Advanced Cardiac Centre, PGIMER, Sector 12, Chandigarh, 160012. Email: [email protected] 2 B.E., M.E., PhD CSE Dept, UIET Panjab University, Chandigarh 160014. 3 M.D., D.M Gastroenterology, Professor, Department of Gastroenterology, PGIMER, Sector 12, Chandigarh, 160012. Email: [email protected] 4 B. Tech., Computer Science, UIET Panjab University, Chandigarh 160014. 5 B.E (Hons)., Biotechnology, Vignan University, Andhra Pradesh 6,9 B.Sc. Hons In Microbiology and Food Technology, MCM Dav College for Women, Sec 36 A, Chandigarh 7,8 M.Sc. Zoology, Post Graduate Government College for Girls, Sector -11 Chandigarh ABSTRACT After few decades, mono-amine hypothesis could grab the attention of millions with the captivating evidence that, prevailing changes in the areas of brain with complex networks of cognitive and emotional behaviors for long time witnessing mood and anxiety disorders. Major Depressive Disorder (MDD) encompasses a large number of psychological illness include, loss of interest, mood disturbance, loss of appetite, insomnia, feeling of fatigue and decreased concentration and standing as the major illness worldwide. Later on, a wealth of data from experimental models started exploring on the environmental factors enhancing the stress which enhances some powerful exerts and induces limbic remodeling or the reduction of synapses pivoted by “Glutamatergic Synapse”.
    [Show full text]
  • The Neurobiology of Treatment-Resistant Depression: from Antidepressant Classifications to Novel Pharmacological Targets
    1521-0081/70/3/475–504$35.00 https://doi.org/10.1124/pr.117.014977 PHARMACOLOGICAL REVIEWS Pharmacol Rev 70:475–504, July 2018 Copyright © 2018 by The American Society for Pharmacology and Experimental Therapeutics ASSOCIATE EDITOR: ELIOT H. OHLSTEIN International Union of Basic and Clinical Pharmacology CIV: The Neurobiology of Treatment-resistant Depression: From Antidepressant Classifications to Novel Pharmacological Targets F. Caraci, F. Calabrese, R. Molteni, L. Bartova, M. Dold, G. M. Leggio, C. Fabbri, J. Mendlewicz, G. Racagni, S. Kasper, M. A. Riva,1 and F. Drago1 Departments of Drug Sciences (F.Car.) and Biomedical and Biotechnological Sciences, School of Medicine (G.M.L., F.D.), University of Catania, Catania, Italy; Oasi-Research-Institute-IRCCS, Troina, Italy (F.Car.); Departments of Pharmacological and Biomolecular Sciences (F.Cal., G.R., M.A.R.) and Medical Biotechnology and Translational Medicine (R.M.), Università degli Studi di Milano, Milan, Italy; Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria (L.B., M.D., S.K.); Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy (C.F.); and School of Medicine, Universite’ Libre de Bruxelles, Bruxelles, Belgium (J.M.) Abstract ...................................................................................476 I. Introduction . ..............................................................................476 Downloaded from II. The New Neuroscience-Based Nomenclature and the Classification of Antidepressant
    [Show full text]
  • Ketamine (C13h16clno)
    Ketamine (C13H16ClNO) Ketamine General Facts Molecular formular: C13H16ClNO Systematic name: 2-(2-chlorophenyl)-2-(methylamino)cyclohexan-1-one (IUPAC name) Alternatenames: a. In medical jargon: Ketaject, Ketanest, dl-Ketamine, Ketalar, CI 581 base, CLSTA 20, Ketolar b. In drug jargon: special K, green, jet, K, and super C Molar mass: 237.092042 g/mol Appearance: white powder, colorless liquid History and Discovery Initial genesis: finding a substitude for Morphin as a anaesthetic initially: Heroin, however too addicting temporary substitute: phencyclidine (PCP) Phencyclidine strong analgesic properties, hallucinogenic effects leading to an introduction in drug world as „angel dust“ 1962: Ketamine as drug with milder side-effects but similar structure 1964: experiments on paid prisoners, first suspicion on effects on psyche 1966: patent by Clarke-Davis 1970: officially in use proven as safe and very effective anaesthetic and painkiller for humans and animals effects strike quickly and does not cause depression or collapse of airways Used for casualties of traffic accidents or battlefield victims Historical usage: Vietnam war as anaesthetic however, still with psychic side effects Synthesis (following the mechanism developed by Calvin L. Stevens) Initial reagent: cyclopentyl Grignard Step 0: Producing cyclopentyl Grignard Reacting cyclopentyl bromide with magnesium in solvent (ether or THF) Best results: distill solvent from Grignard under vacuum and replace with hydrocarbon solvent (e.g. benzene) Step 1: processing to (o-chlorophenyl)-cyclopentyl
    [Show full text]
  • Esketamine Spray Drug to Cure Paralysis
    Editorial Journal of Volume 5:2, 2021 Formulation Science & Bioavailability ISSN: 2577-0543 Open Access Esketamine Spray Drug to Cure Paralysis Ziemandonald* Department of formulation and bioavailability, University of Cologne, Germany Esketamine drug is employed within the treatment of restrictive depression These receptors are liable for the transmission of excitatory chemical signals in adults. In 1997 Esketamine is introduced in medical use and now in March through the Centre systema nervosum and are the key point to strengthen or 5th, 2019 it's approved by FDA for the treatment of depression in adults by weaken the power of the synapses i.e. synaptic plasticity. Like other drugs the nasal route. Oneamong good advantage of Nasal Spray is that it'll act faster common side effects that are observed within the trials are Vomiting, Anxiety, and potentially help those patients which experience suicidal thoughts more and Increase in vital sign , Vomiting, Nausea, dissociation, and Sedation but quickly. it's the non-competitive N-methyl-D-aspartate (NMDA) receptor just in case of efficacy this drug may be a potent and helpful drug to cure antagonist and up to some extent it'll also act on dopamine reuptake inhibitor serious depression. Recently, FDA approved Esketamine drug nasal spray but don't interact with sigma receptor as like ketamine drug. it's a sort of under the name of Spravato or Ketanest to cure severe depression. ketamine drug which is approved by FDA in 1970 which having two chemical The all procedure for that drug has been done by Johnson & Johnson forms R and S and Esketamine contain on of it and that i .e.
    [Show full text]
  • 211243Orig1s000
    CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 211243Orig1s000 OTHER REVIEW(S) MEMORANDUM REVIEW OF REVISED LABEL AND LABELING Division of Medication Error Prevention and Analysis (DMEPA) Office of Medication Error Prevention and Risk Management (OMEPRM) Office of Surveillance and Epidemiology (OSE) Center for Drug Evaluation and Research (CDER) Date of This Memorandum: March 5, 2019 Requesting Office or Division: Division of Psychiatry Products (DPP) Application Type and Number: NDA 211243 Product Name and Strength: Spravato (esketamine) nasal spray, 56 mg dose kit and 84 mg dose kit (28 mg per device) Applicant/Sponsor Name: Janssen Pharmaceuticals, Inc. FDA Received Date: March 5, 2019 (via email) OSE RCM #: 2018-1873-2 DMEPA Safety Evaluator: Loretta Holmes, BSN, PharmD DMEPA Team Leader: Sevan Kolejian, PharmD, MBA 1 PURPOSE OF MEMORANDUM The Division of Psychiatry Products (DPP) requested that we review the device label, blister labeling, carton labeling and Instructions for Use for Spravato (Appendix A) to determine if they are acceptable from a medication error perspective. The revisions are in response to recommendations that we made during a previous label and labeling reviewa and other Agency recommendations provided to Janssen via email. 2 CONCLUSION The revised device label, blister labeling, carton labeling and Instructions for Use for Spravato are acceptable from a medication error perspective. We have no further recommendations at this time. a Holmes, L. Human Factors Results and Label and Labeling Review for Spravato (NDA 211243). Silver Spring (MD): FDA, CDER, OSE, DMEPA (US); 2019 Feb 28. RCM No.: 2018-1875-1 and 2018-1873-1. 1 Reference ID: 4399400 APPENDIX A.
    [Show full text]
  • Brain NMDA Receptors in Schizophrenia and Depression
    biomolecules Review Brain NMDA Receptors in Schizophrenia and Depression Albert Adell 1,2 1 Institute of Biomedicine and Biotechnology of Cantabria, IBBTEC (CSIC-University of Cantabria), Calle Albert Einstein 22 (PCTCAN), 39011 Santander, Spain; [email protected] or [email protected] 2 Biomedical Research Networking Center for Mental Health (CIBERSAM), 39011 Santander, Spain Received: 3 June 2020; Accepted: 21 June 2020; Published: 23 June 2020 Abstract: N-methyl-D-aspartate (NMDA) receptor antagonists such as phencyclidine (PCP), dizocilpine (MK-801) and ketamine have long been considered a model of schizophrenia, both in animals and humans. However, ketamine has been recently approved for treatment-resistant depression, although with severe restrictions. Interestingly, the dosage in both conditions is similar, and positive symptoms of schizophrenia appear before antidepressant effects emerge. Here, we describe the temporal mechanisms implicated in schizophrenia-like and antidepressant-like effects of NMDA blockade in rats, and postulate that such effects may indicate that NMDA receptor antagonists induce similar mechanistic effects, and only the basal pre-drug state of the organism delimitates the overall outcome. Hence, blockade of NMDA receptors in depressive-like status can lead to amelioration or remission of symptoms, whereas healthy individuals develop psychotic symptoms and schizophrenia patients show an exacerbation of these symptoms after the administration of NMDA receptor antagonists. Keywords: NMDA; depression; schizophrenia; subunit; glutamate; GABA 1. Introduction The N-Methyl-D-aspartate (NMDA) receptor (NMDAR) is an ionotropic glutamate receptor that possesses unique characteristics. The flow of ions through the channel is blocked by Mg2+. Two different processes are necessary for activating NMDARs.
    [Show full text]
  • Preclinical and Clinical Studies on LSD, Psilocybin, MDMA, and Ketamine
    The Journal of Neuroscience, February 3, 2021 • 41(5):891–900 • 891 Symposium/Mini-Symposium Hallucinogens in Mental Health: Preclinical and Clinical Studies on LSD, Psilocybin, MDMA, and Ketamine Danilo De Gregorio,1 Argel Aguilar-Valles,2p Katrin H. Preller,3p Boris Dov Heifets,4p Meghan Hibicke,5p Jennifer Mitchell,6p and Gabriella Gobbi1 1Department of Psychiatry, McGill University, Montreal, Quebec H3A 1A1, Canada, 2Department of Neuroscience, Carleton University, Ottawa, Ontario K1S 5B6, Canada, 3Department of Psychiatry, Psychotherapy and Psychosomatics, University of Zurich, CH-8032 Zurich, Switzerland, 4Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, California 94305, 5Department of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, and 6Department of Neurology, University of California San Francisco, San Francisco, California 94158 A revamped interest in the study of hallucinogens has recently emerged, especially with regard to their potential application in the treatment of psychiatric disorders. In the last decade, a plethora of preclinical and clinical studies have confirmed the efficacy of ketamine in the treatment of depression. More recently, emerging evidence has pointed out the potential therapeu- tic properties of psilocybin and LSD, as well as their ability to modulate functional brain connectivity. Moreover, MDMA, a compound belonging to the family of entactogens, has been demonstrated to be useful to treat post-traumatic stress disor- ders. In this review, the pharmacology of hallucinogenic compounds is summarized by underscoring the differences between psychedelic and nonpsychedelic hallucinogens as well as entactogens, and their behavioral effects in both animals and humans are described. Together, these data substantiate the potentials of these compounds in treating mental diseases.
    [Show full text]
  • APSF3502.Pdf
    APSF.ORG NEWSLETTER THE OFFICIAL JOURNAL OF THE ANESTHESIA PATIENT SAFETY FOUNDATION Volume 35, No. 2, 33–68 More than 1,000,000 readers annually worldwide June 2020 Disclaimer: Viewers of this material should review the information contained within it with appropriate medical and legal counsel and make their own determinations as to relevance to their particular practice setting and compliance with state and federal laws and regulations. The APSF has used its best efforts to provide accurate information. However, this material is provided only for informational purposes and does not constitute medical or legal advice. These articles also should not be construed as representing APSF endorsement or policy (unless otherwise stated), making clinical recommendations, or substituting for the judgment of a physician and consultation with independent legal counsel. An Update on the Perioperative Considerations for COVID-19 Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) by Liana Zucco, MD; Nadav Levy, MD; Desire Ketchandji, MD; Michael Aziz, MD; and Satya Krishna Ramachandran, MD INTRODUCTION over 3.1 million people, as of April 29, 2020, with 1,2 The COVID-19 pandemic caused by the over 1 million cases in the United States alone. severe acute respiratory syndrome coronavirus-2 Current estimates suggest a fatality rate (SARS-CoV-2) continues to have a profound ranging from 2 to 20% for hospitalized patients, impact on life across the globe and has placed and up to 88% for those requiring mechanical 3–5 an enormous strain on health care systems and ventilation. SARS-CoV-2 has an estimated basic reproductive number (R0) of 2.2–2.7,6 economies, including with likely untold psycho- which means a single infected person has the logical and social implications.
    [Show full text]
  • Psychedelic Report
    OCEAN WALL PSYCHEDELICS May 2021 EXECUTIVE SUMMARY Psychedelics has seen huge increase in investment focus in the last few years, but for many it remains a misunderstood, much maligned, and extremely niche sector. Here we seek to give you its history, research - past and present, who are the companies involved – established and start-up – big and small – public and private, and who the big investors in this sector are. Investors are now actively investing in psychedelic medicine. Recent reports indicate that the global market for functional mushrooms, is forecasted to reach $34.3 billion by 2024 and continues growing at a respectable CAGR of 8%.1 Unlike cannabis, which remains federally illegal in the U.S., the work psychedelic companies are doing is legal. This creates a greater opportunity to access growth capital from private investors who may not want to touch cannabis. It also sets the industry apart with it also being a more concentrated space because the barriers to entry are much higher.2 The U.S. Food and Drug Administration (USFDA) status on the use of psychedelics appears to be quickly evolving, following the breakthrough therapy status for treatment-resistant depression in 2020 which appears poised to receive approvals in 2021. Back in December 2019, a ketamine-like drug – esketamine – was licenced for use in the UK as a rapid onset treatment for major depression, and in December 2020, regulators approved UK’s Small Pharma to conduct the world’s first clinical trial to explore DMT as a treatment for depression. With mental health becoming a global problem – which has only been exasperated by the COVID pandemic – there is real urgency to find alternative and new treatments.
    [Show full text]