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      Injectable anti-malarials revisited: discovery and development of new agents to protect against malaria

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          Abstract

          Over the last 15 years, the majority of malaria drug discovery and development efforts have focused on new molecules and regimens to treat patients with uncomplicated or severe disease. In addition, a number of new molecular scaffolds have been discovered which block the replication of the parasite in the liver, offering the possibility of new tools for oral prophylaxis or chemoprotection, potentially with once-weekly dosing. However, an intervention which requires less frequent administration than this would be a key tool for the control and elimination of malaria. Recent progress in HIV drug discovery has shown that small molecules can be formulated for injections as native molecules or pro-drugs which provide protection for at least 2 months. Advances in antibody engineering offer an alternative approach whereby a single injection could potentially provide protection for several months. Building on earlier profiles for uncomplicated and severe malaria, a target product profile is proposed here for an injectable medicine providing long-term protection from this disease. As with all of such profiles, factors such as efficacy, cost, safety and tolerability are key, but with the changing disease landscape in Africa, new clinical and regulatory approaches are required to develop prophylactic/chemoprotective medicines. An overall framework for these approaches is suggested here.

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          Gamma-globulin and acquired immunity to human malaria.

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            Malaria

            Malaria is caused in humans by five species of single-celled eukaryotic Plasmodium parasites (mainly Plasmodium falciparum and Plasmodium vivax) that are transmitted by the bite of Anopheles spp. mosquitoes. Malaria remains one of the most serious infectious diseases; it threatens nearly half of the world's population and led to hundreds of thousands of deaths in 2015, predominantly among children in Africa. Malaria is managed through a combination of vector control approaches (such as insecticide spraying and the use of insecticide-treated bed nets) and drugs for both treatment and prevention. The widespread use of artemisinin-based combination therapies has contributed to substantial declines in the number of malaria-related deaths; however, the emergence of drug resistance threatens to reverse this progress. Advances in our understanding of the underlying molecular basis of pathogenesis have fuelled the development of new diagnostics, drugs and insecticides. Several new combination therapies are in clinical development that have efficacy against drug-resistant parasites and the potential to be used in single-dose regimens to improve compliance. This ambitious programme to eliminate malaria also includes new approaches that could yield malaria vaccines or novel vector control strategies. However, despite these achievements, a well-coordinated global effort on multiple fronts is needed if malaria elimination is to be achieved.
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              Strategies for extended serum half-life of protein therapeutics.

              With a growing number of protein therapeutics being developed, many of them exhibiting a short plasma half-life, half-life extension strategies find increasing attention by the biotech and pharmaceutical industry. Extension of the half-life can help to reduce the number of applications and to lower doses, thus are beneficial for therapeutic but also economic reasons. Here, a comprehensive overview of currently developed half-life extension strategies is provided including those aiming at increasing the hydrodynamic volume of a protein drug but also those implementing recycling processes mediated by the neonatal Fc receptor. Copyright © 2011 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                wellst@mmv.org
                Journal
                Malar J
                Malar. J
                Malaria Journal
                BioMed Central (London )
                1475-2875
                1 November 2018
                1 November 2018
                2018
                : 17
                : 402
                Affiliations
                [1 ]ISNI 0000 0004 0432 5267, GRID grid.452605.0, Medicines for Malaria Venture, ; Route de Pré Bois 20, 1215 Geneva, Switzerland
                [2 ]ISNI 0000 0004 0623 0341, GRID grid.419619.2, Drug Product Development, , Janssen R&D, Johnson & Johnson, ; Turnhoutseweg 30, 2340 Beerse, Belgium
                [3 ]ISNI 0000 0001 0672 1325, GRID grid.11702.35, Department of Science and Environment, , Roskilde University, ; 4000 Roskilde, Denmark
                [4 ]ISNI 0000 0004 0425 469X, GRID grid.8991.9, Faculty of Infectious and Tropical Diseases, , London School of Hygiene and Tropical Medicine, ; London, UK
                Author information
                http://orcid.org/0000-0002-2261-9424
                Article
                2549
                10.1186/s12936-018-2549-1
                6211409
                30384848
                d6b8b6e1-3538-44ee-b3bd-2251068b22a1
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 September 2018
                : 24 October 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004167, Medicines for Malaria Venture;
                Categories
                Review
                Custom metadata
                © The Author(s) 2018

                Infectious disease & Microbiology
                malaria,plasmodium,chemoprotection,prophylaxis,liver schizont,intra-muscular,target candidate profile,target product profile

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