P Winstanley

Summary

Affiliation: University of Liverpool
Country: UK

Publications

  1. ncbi Beyond registration--measuring the public-health potential of new treatments for malaria in Africa
    Trudie Lang
    GlaxoSmithKline, Department for Diseases of the Developing World
    Lancet Infect Dis 6:46-52. 2006
  2. ncbi Chlorproguanil/dapsone for uncomplicated Plasmodium falciparum malaria in young children: pharmacokinetics and therapeutic range
    P Winstanley
    Kenya Medical Research Institute KEMRI, CRC Research Unit, Kilifi, Kenya
    Trans R Soc Trop Med Hyg 91:322-7. 1997
  3. ncbi Therapy of falciparum malaria in sub-saharan Africa: from molecule to policy
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool L69 3GE, United Kingdom
    Clin Microbiol Rev 17:612-37, table of contents. 2004
  4. ncbi The contribution of clinical pharmacology to antimalarial drug discovery and development
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, UK
    Br J Clin Pharmacol 55:464-8. 2003
  5. ncbi Coping with malaria in the face of resistance
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK
    Int J Infect Dis 6:246-52. 2002
  6. ncbi Clinical status and implications of antimalarial drug resistance
    Peter A Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, L69 3GE, Liverpool, UK
    Microbes Infect 4:157-64. 2002
  7. ncbi Modern chemotherapeutic options for malaria
    P Winstanley
    Department of Pharmacology and Therapeutics, and Wellcome Trust Centre for Research in Clinical Tropical Medicine, University of Liverpool, UK
    Lancet Infect Dis 1:242-50. 2001
  8. ncbi Chlorproguanil-dapsone (LAPDAP) for uncomplicated falciparum malaria
    P Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, UK
    Trop Med Int Health 6:952-4. 2001
  9. ncbi Chemotherapy for falciparum malaria: the armoury, the problems and the prospects
    P A Winstanley
    Department of Pharmacology and Therapeutics, The University of Liverpool, UK L69 3GE
    Parasitol Today 16:146-53. 2000
  10. ncbi Population pharmacokinetic and pharmacodynamic modelling of the antimalarial chemotherapy chlorproguanil/dapsone
    Julie A Simpson
    Cancer Epidemiology Centre, The Cancer Council Victoria, Melbourne, Australia
    Br J Clin Pharmacol 61:289-300. 2006

Collaborators

Detail Information

Publications16

  1. ncbi Beyond registration--measuring the public-health potential of new treatments for malaria in Africa
    Trudie Lang
    GlaxoSmithKline, Department for Diseases of the Developing World
    Lancet Infect Dis 6:46-52. 2006
    ....
  2. ncbi Chlorproguanil/dapsone for uncomplicated Plasmodium falciparum malaria in young children: pharmacokinetics and therapeutic range
    P Winstanley
    Kenya Medical Research Institute KEMRI, CRC Research Unit, Kilifi, Kenya
    Trans R Soc Trop Med Hyg 91:322-7. 1997
    ..These data, together with the clinical trial, will be helpful in deciding whether current chlorproguanil/dapsone doses are optimal for the treatment of falciparum malaria...
  3. ncbi Therapy of falciparum malaria in sub-saharan Africa: from molecule to policy
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool L69 3GE, United Kingdom
    Clin Microbiol Rev 17:612-37, table of contents. 2004
    ..The review also discusses the splicing of new drugs into national policy. The various parameters that feed into deliberations on changes in drug policy are discussed...
  4. ncbi The contribution of clinical pharmacology to antimalarial drug discovery and development
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, UK
    Br J Clin Pharmacol 55:464-8. 2003
    ..Although effective drugs are available, they are largely too expensive for routine use. The present article reviews the ways in which clinical pharmacology has contributed to the identification of new drugs and strategies for malaria...
  5. ncbi Coping with malaria in the face of resistance
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK
    Int J Infect Dis 6:246-52. 2002
  6. ncbi Clinical status and implications of antimalarial drug resistance
    Peter A Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, L69 3GE, Liverpool, UK
    Microbes Infect 4:157-64. 2002
    ..Artemisinin combination therapy may offer considerable advantages over alternative therapies, but its introduction faces considerable logistic difficulty...
  7. ncbi Modern chemotherapeutic options for malaria
    P Winstanley
    Department of Pharmacology and Therapeutics, and Wellcome Trust Centre for Research in Clinical Tropical Medicine, University of Liverpool, UK
    Lancet Infect Dis 1:242-50. 2001
    ..The article then examines the challenges faced in the processes of changing policy, and the implementation of that policy shift...
  8. ncbi Chlorproguanil-dapsone (LAPDAP) for uncomplicated falciparum malaria
    P Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, UK
    Trop Med Int Health 6:952-4. 2001
    ..This short paper outlines the current stages that LAPDAP and CDA have reached, and sketches the anticipated public health issues...
  9. ncbi Chemotherapy for falciparum malaria: the armoury, the problems and the prospects
    P A Winstanley
    Department of Pharmacology and Therapeutics, The University of Liverpool, UK L69 3GE
    Parasitol Today 16:146-53. 2000
    ..He then examines some of the current major problems and prospects for the future...
  10. ncbi Population pharmacokinetic and pharmacodynamic modelling of the antimalarial chemotherapy chlorproguanil/dapsone
    Julie A Simpson
    Cancer Epidemiology Centre, The Cancer Council Victoria, Melbourne, Australia
    Br J Clin Pharmacol 61:289-300. 2006
    ....
  11. ncbi Why has the dihydrofolate reductase 164 mutation not consistently been found in Africa yet?
    Alexis Nzila
    Kenya Medical Research Institute Wellcome Trust Collaborative Research Program, Wellcome Trust Research Laboratories, P O Box 43640, 00100 GPO, Nairobi, Kenya
    Trans R Soc Trop Med Hyg 99:341-6. 2005
    ..In this paper, we discuss briefly the reasons why Leu-164 has not yet been selected in Africa and we propose a means that may slow down the selection of this mutation...
  12. ncbi Malaria chemotherapy
    Peter Winstanley
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool L69 3GE, UK
    Adv Parasitol 61:47-76. 2006
    ..We give no apology for placing our emphasis upon the use of antimalarial drugs in endemic populations rather than their use for prophylaxis in travellers...
  13. ncbi Current issues in the treatment of uncomplicated malaria in Africa
    David Bell
    Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool L69 3GE, UK
    Br Med Bull 71:29-43. 2004
    ..This article reviews the rationale behind combination therapy, the drugs available and the available evidence from combination therapy trials in Africa. Treatment of uncomplicated malaria in pregnancy and infants is also discussed...
  14. ncbi Chemosensitization of Plasmodium falciparum by probenecid in vitro
    Alexis Nzila
    Kenya Medical Research Institute Wellcome Trust Collaborative Research Program, Wellcome Trust Research Laboratories, Nairobi, Kenya
    Antimicrob Agents Chemother 47:2108-12. 2003
    ..P. Thompson & Co., Liverpool, United Kingdom] has been filed to protect this intellectual property)...
  15. ncbi The potential for interactions between antimalarial and antiretroviral drugs
    Saye Khoo
    AIDS 19:995-1005. 2005
  16. ncbi Developmental toxicity of artesunate and an artesunate combination in the rat and rabbit
    Robert L Clark
    Safety Assessment, GlaxoSmithKline, King of Prussia, Pa 19406 0939, USA
    Birth Defects Res B Dev Reprod Toxicol 71:380-94. 2004
    ..Investigations of the mechanism of developmental toxicity are ongoing to attempt to determine whether rats and rabbits are more sensitive to artemisinins than humans...