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PRIORITIZATION OF PATHOGENS TO GUIDE DISCOVERY, RESEARCH AND DEVELOPMENT OF NEW ANTIBIOTICS FOR DRUG-RESISTANT BACTERIAL INFECTIONS, INCLUDING TUBERCULOSIS 1 PRIORITIZATION OF PATHOGENS TO GUIDE DISCOVERY, RESEARCH AND DEVELOPMENT OF NEW ANTIBIOTICS FOR DRUG-RESISTANT BACTERIAL INFECTIONS, INCLUDING TUBERCULOSIS PRIORITIZATION OF PATHOGENS TO GUIDE DISCOVERY, RESEARCH AND DEVELOPMENT OF NEW ANTIBIOTICS FOR DRUG-RESISTANT BACTERIAL INFECTIONS, INCLUDING TUBERCULOSIS WHO/EMP/IAU/2017.12 © World Health Organization 2017 Some rights reserved. This work is available under the Creative Commons Attribution- NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons. org/licenses/by-nc-sa/3.0/igo). Under the terms of this licence, you may copy, redistribute and adapt the work for non-commercial purposes, provided the work is appropriately cited, as indicated below. In any use of this work, there should be no suggestion that WHO endorses any specific organization, products or services. The use of the WHO logo is not permitted. If you adapt the work, then you must license your work under the same or equivalent Creative Commons licence. If you create a translation of this work, you should add the following disclaimer along with the suggested citation: “This translation was not created by the World Health Organization (WHO). WHO is not responsible for the content or accuracy of this translation. The original English edition shall be the binding and authentic edition”. Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization. Suggested citation. Prioritization of pathogens to guide discovery, research and development of new antibiotics for drug-resistant bacterial infections, including tuberculosis. Geneva: World Health Organization; 2017(WHO/EMP/IAU/2017.12). ( Licence: CC BY-NC-SA 3.0 IGO.. Cataloguing-in-Publication (CIP) data. CIP data are available at http://apps.who.int/iris. Sales, rights and licensing. To purchase WHO publications, see http://apps.who.int/bookorders. To submit requests for commercial use and queries on rights and licensing, see http://www.who. int/about/licensing. Third-party materials. If you wish to reuse material from this work that is attributed to a third party, such as tables, figures or images, it is your responsibility to determine whether permission is needed for that reuse and to obtain permission from the copyright holder. The risk of claims resulting from infringement of any third-party-owned component in the work rests solely with the user. General disclaimers. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of WHO concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by WHO in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by WHO to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader. In no event shall WHO be liable for damages arising from its use. Printed in Geneva, Switzerland Foreword further increases the burden of infectious diseases. Low-income countries are particularly vulnerable because of conditions that enable the spread of these diseases, such as poor sanitation, lack of control of and guidance on antibiotic use, inadequate health- care services and systems, and limited or inadequate infection control measures. Middle- and upper-middle-income countries are not free of the burden of drug resistance, however. BRICS countries (Brazil, Russian Federation, India, China and South Africa) and several European countries face major epidemics of multidrug-resistant infections caused by common Gram-negative bacteria and multidrug-resistant-TB (MDR-TB), with devastating public health and economic consequences. Sadly, the pipeline for new antibiotics currently includes only a small number of novel compounds in development. In the past 20 years, only two new antibiotic classes, both active only against Gram-positive bacteria, have received global regulatory approval by international regulatory agencies. In the same time period, no new Infectious diseases are among the top 10 causes of antibiotics against Gram-negative bacteria have been death and the leading cause of disability-adjusted life approved. In addition, only two completely new drugs years worldwide. Among these, acute lower respiratory for MDR-TB treatment (bedaquiline and delamanid) tract infections, diarrhoeal diseases and tuberculosis have reached the market in over 70 years. (TB) are responsible for significant global morbidity and mortality. The overall burden of communicable In 2016, at the high-level meeting of the UN General diseases is strongly linked to poverty and, as a result, Assembly on antimicrobial resistance, Heads of State the African continent still suffers from the highest directed an unprecedented level of attention to curbing mortality from infectious diseases. the spread of infections that are resistant to antimicrobial medicines. They reaffirmed their commitment to The reasons for the emergence and re-emergence stopping the misuse of antimicrobial medicines of infectious diseases worldwide include a in human health, animal health and agriculture, breakdown of public health measures in the face of and recognized the need for stronger systems to epidemic transitions, increasing international travel, monitor drug-resistant infections and the amounts immigration for political, social and economic of antimicrobials used in humans and animals. In the reasons, microbe adaptation and ability to change, wake of the increasing global awareness of the need and transmission of several pathogens between for new antibiotics, Member States highlighted market animals and humans. Of great concern is the global failures, and called for new incentives for investment emergence of resistance of infectious pathogens to in research and development of new, effective and many first-line medicines. affordable medicines, rapid diagnostic tests, and other important therapies to replace those that are losing Equitable access to medicines is another major concern their effectiveness. In response to this and in line with in many low- and middle-income countries where the Global Action Plan on Antimicrobial Resistance to common, treatable infections like pneumonia and TB support the identification of pathogens of greatest are still associated with high numbers of deaths, often in concern, WHO developed a priority list of antibiotic- children. The emergence of pathogenic microbes with resistant bacteria to underpin renewed efforts for the drug resistance, not only to the most commonly used research and development of new antibiotics. antibiotics but also to second-line, “reserve” medicines, 2016 was also the first year of implementation of development of new antibiotics to treat drug-resistant the WHO End TB Strategy, which was adopted by bacterial infections and TB. It is acknowledged that the World Health Assembly in 2014 and aimed at viral, fungal and parasitic infections may well need a attaining universal access to TB prevention, diagnosis similar strategy in the near future. The development and treatment. Global TB care and control measures of new antibiotics to tackle the serious problem of saved an estimated 49 million lives between 2000 and drug-resistant infections needs to be prioritized 2015, yet widespread MDR-TB threatens to reverse in the global political agenda of world leaders and the gains made from decades of effort to contain the health policy-makers. It also needs to be linked to TB epidemic. MDR-TB was declared a global crisis by the development of appropriate health-care delivery WHO in 2014, 21 years after TB had been declared services and to proper stewardship to safeguard the a global emergency (in 1993) and despite greatly use of current and future medicines. This challenge improved cure rates in patients with drug-susceptible cannot be simplified in a “one size fits all” approach. TB. The TB emergency prompted the establishment The only possible defence against the threat of of new financing mechanisms to support countries antimicrobial resistance and the (very real) possibility in tackling the TB epidemic, most notably the Global of a post-antibiotic era is a global and coordinated Fund and Unitaid. However, investment in research effort by all stakeholders. This document reflects and development for TB has major gaps in the funding the commitment and contribution of WHO and needed to develop new tools that would help achieve its partners to help establish priorities for critically the targets of the WHO End TB Strategy. needed research and development on new antibiotics against drug-resistant bacterial infections and TB, in The overall goal of the following report is to present line with our mission of ensuring health for all. the priority pathogens to be targeted for research and Dr Tedros Adhanom Ghebreyesus WHO Director-General Contents Acknowledgements 8 Executive summary 10 Introduction 14 Section 1: Tuberculosis 15 1.1 A top infectious disease killer 15 1.2 MDR-TB: a global public health crisis and health security threat 17 1.3 Arduous, toxic and limited treatment options 21 1.4 Profound human suffering and health service dilemmas 21 1.5 Critical gaps in investment in research and development 22 Section 2: Ranking of other drug-resistant bacterial infections 25 2.1 Background 25 2.2 Selection of prioritization methodology 29 2.3 Multi-criteria decision analysis: methodology for the prioritization exercise 39 2.3.1 Expert group selection 40 2.3.2 Selection of antibiotic-resistant bacteria to be prioritized 40 2.3.3 Selection of criteria for prioritization 44 2.3.4 Data extraction and criteria synthesis into the MCDA model 46 2.3.5 Summary of the evidence assessment methods: 62 strengths and limitations 2.3.6 Summary of the evidence 64 2.3.7 Ranking 75 2.4 Survey results 76 2.5 Ranking of other drug-resistant bacterial infections: overall results 79 2.6 Conclusions 80 References 83 Acknowledgements The development of this report was a collaborative Advisory group process between the WHO Department of Essential ∞ Marco Cavaleri: European Medicines Agency, Medicines and Health Products (EMP) and the WHO London, UK Global Tuberculosis Programme (GTB), overseen by ∞ Edward M. Cox: US Food and Drug Suzanne Hill (Director, EMP) and Mario Raviglione Administration, Washington, USA (Director, GTB). ∞ Paul Hansen: University of Otago, Dunedin, New The report comprises two main sections. Zealand Section 1 describes the current situation with respect ∞ Chris R. Houchens: Antibacterials Program to TB and was prepared by Karin Weyer (WHO, GTB). Biomedical Advanced Research and Development Authority, Washington, USA Sections 2 reports the methods and results of the ∞ M. Lindsay Grayson: Austin Health, University of multi-criteria decision analysis used to prioritize other Melbourne, Melbourne, Australia antibiotic-resistant bacteria and was prepared by ∞ Dominique L. Monnet: European Centre for Evelina Tacconelli (Tübingen University Hospital, DZIF Disease Prevention and Control, Stockholm, Partner Center, Germany), and Nicola Magrini (WHO Sweden EMP) in collaboration with members of the WHO Priority Pathogens List (PPL) coordinating, advisory and ∞ Marc Ouellette: Laval University and Canadian working groups. The contributions of the following Institutes for Health Research, Québec, Canada individuals are gratefully acknowledged: ∞ Kevin Outterson: Combating Antibiotic Resistant Bacteria Biopharmaceutical Accelerator, Boston University, Boston, USA Coordinating group ∞ Jean Patel: Centers for Disease Control and ∞ Yehuda Carmeli: Tel Aviv University, Tel Aviv, Israel Prevention, Atlanta, USA ∞ Elena Carrara: Tübingen University Hospital, DZIF Center, Tübingen, Germany Working group ∞ Stephan Harbarth: Geneva University Hospitals Aaron O. Aboderin (Nigeria), Seif S. Al-Abri (Oman), and Faculty of Medicine, Geneva, Switzerland Nordiah Awang Jalil (Malaysia), Nur Benzonana ∞ Gunnar Kahlmeter: Central Hospital, Växjö, (Turkey), Sanjay Bhattacharya (India), Adrian John Brink Sweden (South Africa), Francesco Robert Burkert (Germany), ∞ Jan Kluytmans: University Medical Center, Otto Cars (Sweden), Giuseppe Cornaglia (Italy), Oliver Utrecht, Amphia Hospital, Breda, the Netherlands James Dyar (Sweden), Alexander W. Friedrich (the Netherlands), Ana C. Gales (Brazil), Sumanth Gandra ∞ Marc Mendelson: Groote Schuur Hospital, University of Cape Town, Cape Town, South (India), Christian G. Giske (Sweden), Debra A. Goff Africa (USA), Herman Goossens (Belgium), Thomas Gottlieb (Australia), Manuel Guzman Blanco (Venezuela), ∞ Céline Pulcini: Nancy University Hospital, Lorraine Waleria Hryniewicz (Poland), Deepthi Kattula (India), University, EA 4360 APEMAC, Nancy, France Timothy Jinks (UK), Souha S. Kanj (Lebanon), Lawrence ∞ Alessia Savoldi: Tübingen University Hospital, DZIF Kerr (USA), Marie-Paule Kieny (WHO), Yang Soo Center, Tübingen, Germany Kim (South Korea), Roman S. Kozlov (Russia), Jaime ∞ Nalini Singh: Children’s National Health System, Labarca (Chile), Ramanan Laxminarayan (USA), Karin George Washington University, Washington, USA Leder (Australia), Leonard Leibovici (Israel), Gabriel Levy Hara (Argentina), Jasper Littman (Germany), ∞ Ursula Theuretzbacher: Center for Anti-infective Surbhi Malothra-Kumar (Belgium), Vikas Manchanda Agents, Vienna, Austria 8 (India), Lorenzo Moja (WHO), Babacar Ndoye (Senegal), For all experts, advice was provided in their personal Angelo Pan (Italy), David Paterson (Australia), Mical Paul capacity. The views in this report do not necessarily (Israel), Haibo Qiu (China), Pilar Ramon-Pardo (USA), reflect and should not be interpreted as being the Jesús Rodríguez-Baño (Spain), Maurizio Sanguinetti official position of any agency or institution. (Italy), Sharmila Sengupta (India), Mike Sharland (UK), Funding provided by the Government of Germany Massinissa Si-Mehand (WHO), Lynn L. Silver (USA), for the development of the Priority Pathogens List is Wonkeung Song (South Korea), Martin Steinbakk gratefully acknowledged. (Norway), Jens Thomsen (United Arab Emirates), Guy E. Thwaites (UK), Jos van der Meer (the Netherlands), Nguyen Van Kinh (Vietnam), Silvio Vega (Panama), Maria Virginia Villegas (Colombia), Agnes Wechsler-Fördös (Austria), Heiman F. L. Wertheim (the Netherlands), Evelyn Wesangula (Kenya), Neil Woodford (UK), Fidan O. Yilmaz (Azerbaijan), Anna Zorzet (Sweden). 9 Executive summary Antimicrobial resistance is one of the most complex for new antibiotics, and to support the implementation global health challenges today. The world has long of the Global Action Plan on Antimicrobial Resistance, ignored warnings that antibiotics and other medicines WHO developed a priority pathogens list (PPL) of are losing their effectiveness after decades of overuse antibiotic-resistant bacteria to support research and and misuse in human medicine, animal health and development into new and effective drugs. This action agriculture. Common illnesses like pneumonia, post- also followed recommendations in the 2016 United operative infections, diarrhoeal and sexually transmitted Nations report of a high-level panel on the global diseases, as well as the world’s largest infectious response to health crises, which emphasized the disease killers – tuberculosis (TB), HIV and malaria – threat posed to humanity from a number of under- are increasingly becoming untreatable because of the researched antibiotic-resistant bacteria that urgently emergence and spread of drug resistance. require enhanced and focused investment in research and development. Worsening antimicrobial resistance could have serious public health, economic and social implications. The 2016 was also the first year of implementation of the threat of antimicrobial resistance is also becoming WHO End TB strategy, which was adopted by the World a key consideration for programmes addressing Health Assembly in 2014. The End TB Strategy serves maternal and child health, sexual and reproductive as the core strategic document for all WHO Member health, foodborne diseases, water and sanitation, and States on TB prevention, control and elimination, infection prevention and control. The World Bank including the prevention and management of TB drug has warned that antimicrobial resistance could cause resistance. The End TB strategy is an evolution of the more economic damage than the 2008 financial crisis. 2006 WHO Stop TB Strategy and its predecessor, And although the 21st century is being shaped by the 1995 WHO DOTS Strategy, which Member States technology and innovation, humans could soon find started to implement after WHO declared TB a global themselves in an era where simple infections once health emergency in 1993. Twenty-one years later, in again kill millions every year. 2014, multidrug-resistant TB (MDR-TB) was declared a global public health crisis by WHO, with a call urging The past three years have seen unprecedented increased investment in research and development, global political momentum to address antimicrobial especially for new drugs and diagnostics. resistance: in 2015, governments adopted a global action plan at the World Health Assembly and in 2016 Prioritization of pathogens for research and passed a political declaration at the United Nations development is highly challenging given the absence General Assembly. Antimicrobial resistance has made of established criteria defining the impact of pathogens it onto the agendas of the G7 and G20 groups and is a on human health. As a result, no consensus exists core component of the Global Health Security Agenda. on the most effective methodology to develop prioritization in infectious diseases. Ranking antibiotic- WHO is working closely with the Food and Agriculture resistant organisms to direct future research and Organization of the United Nations and the World development requires a detailed identification and Organization for Animal Health in leading global efforts integration of extensive information that defines the against antimicrobial resistance and ensuring that the burden of antimicrobial resistance (microbiological, necessary momentum is consolidated and sustained. epidemiological, and clinical). Moreover, communicable These efforts are guided by an ad-hoc interagency diseases differ in clinical presentation and duration coordination group established in 2017. A global (e.g. acute versus chronic), treatment approaches (e.g. development and stewardship framework to combat multidrug versus single drug therapy), and etiology (e.g. antimicrobial resistance is being drafted to support bacterial, viral, fungal). the development of new antimicrobial medicines, diagnostics, vaccines and other tools. The diversity of communicable diseases is a major challenge for prioritization of pathogens. As a One of the gravest global concerns about antimicrobial result, the scope and focus of the work underlying resistance currently is that antibiotic resistance has this document was agreed beforehand to allow emerged in so many pathogens, including TB. In 2016, in the deliverables requested by Member States to be the wake of the increasing global awareness of the need 10

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new antibiotics for drug-resistant bacterial infections, including tuberculosis. Geneva: World .. Antimicrobial resistance is one of the most complex.
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