Skip to main content
Top
Published in: Clinical Pharmacokinetics 9/2020

Open Access 01-09-2020 | Antibiotic | Review Article

Preclinical Pharmacokinetic/Pharmacodynamic Studies and Clinical Trials in the Drug Development Process of EMA-Approved Antibacterial Agents: A Review

Authors: Anselm Jorda, Markus Zeitlinger

Published in: Clinical Pharmacokinetics | Issue 9/2020

Login to get access

Abstract

Development of new antibacterial agents is necessary as drug-resistant bacteria are a threat to global health. In Europe, the European Medicines Agency has been guiding this development process for more than two decades. We investigated preclinical and clinical pre-approval studies to illuminate the current authorization process with emphasis on pharmacokinetic/pharmacodynamic approaches and clinical phases. All centrally authorized systemic antibacterial and antimycobacterial drugs within the European Union were included without any time restriction. Additionally, US Food and Drug Administration-approved antibiotics of the previous 3 years, which were not yet approved by the European Medicines Agency, were included. We focused on preclinical pharmacokinetic/pharmacodynamic studies and phase II and phase III clinical trials. Furthermore, we looked at the recommended dosing regimens and approved indications. In this review, we designed tree diagrams as a new means of illustrating the development process of antibiotics to relate pharmacokinetic/pharmacodynamic phase II and III studies to approved indications. We included 23 (European Medicines Agency, 18; US Food and Drug Administration, 5) antimicrobial agents. Tetracyclines, carbapenems, and cephalosporins were the leading classes. The recommended dosing intervals were significantly shorter in time- vs exposure-dependent drugs (median 8 vs 12, p = 0.006). The majority of approved indications (i.e., acute bacterial skin and soft-tissue infection, community-acquired pneumonia, complicated intra-abdominal infection, complicated urinary tract infection, and complicated skin and soft-tissue infection) used non-inferiority trials. Phase II and III clinical trials investigating community-acquired pneumonia involved the fewest patients. Some promising drugs were marketed in recent years; the individual steps to their authorizations are illuminated. We confirmed the relevance of preclinical pharmacokinetic/pharmacodynamic studies in dosing optimization and decision making in antimicrobial drug development. Non-inferiority clinical trials predominated.
Literature
1.
go back to reference World Health Organization. Global antimicrobial resistance surveillance system (GLASS) report: early implementation 2016–2017. Geneva: World Health Organization; 2017. World Health Organization. Global antimicrobial resistance surveillance system (GLASS) report: early implementation 2016–2017. Geneva: World Health Organization; 2017.
2.
go back to reference Global Health Metrics. Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2017;390(10100):1151–210.CrossRef Global Health Metrics. Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2017;390(10100):1151–210.CrossRef
3.
go back to reference Woods K, Wathion N. European Medicines Agency: 20th anniversary book. London: Core Media Services UK Ltd.; 2015. Woods K, Wathion N. European Medicines Agency: 20th anniversary book. London: Core Media Services UK Ltd.; 2015.
5.
go back to reference EMA-CHMP. Guideline on the evaluation of medicinal products indicated for the treatment of bacterial infections: revision 3 (EMA/844951/2018). London: European Medicines Agency; 2018. EMA-CHMP. Guideline on the evaluation of medicinal products indicated for the treatment of bacterial infections: revision 3 (EMA/844951/2018). London: European Medicines Agency; 2018.
6.
go back to reference EMA-CHMP. Addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections (EMA/CHMP/351889/2013). London: European Medicines Agency; 2013. EMA-CHMP. Addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections (EMA/CHMP/351889/2013). London: European Medicines Agency; 2013.
7.
go back to reference EMA-CHMP. Guideline on the use of pharmacokinetics and pharmacodynamics in the development of antimicrobial medicinal products (EMA/CHMP/594085/2015). London: European Medicines Agency; 2016. EMA-CHMP. Guideline on the use of pharmacokinetics and pharmacodynamics in the development of antimicrobial medicinal products (EMA/CHMP/594085/2015). London: European Medicines Agency; 2016.
24.
go back to reference EMA-ICH. E8: general considerations for clinical trials: Step 5 (CPMP/ICH/291/95). London: European Medicines Agency; 1998. EMA-ICH. E8: general considerations for clinical trials: Step 5 (CPMP/ICH/291/95). London: European Medicines Agency; 1998.
27.
go back to reference Projan SJ. Why is big Pharma getting out of antibacterial drug discovery? Curr Opin Microbiol. 2003;6(5):427–30.CrossRef Projan SJ. Why is big Pharma getting out of antibacterial drug discovery? Curr Opin Microbiol. 2003;6(5):427–30.CrossRef
33.
go back to reference EMA. Applications for new human medicines under evaluation by the Committee for Medicinal Products for Human Use. Amsterdam: European Medicines Agency; 2019. EMA. Applications for new human medicines under evaluation by the Committee for Medicinal Products for Human Use. Amsterdam: European Medicines Agency; 2019.
38.
go back to reference Hidalgo JA, Vinluan CM, Antony N. Ceftazidime/avibactam: a novel cephalosporin/nonbeta-lactam beta-lactamase inhibitor for the treatment of complicated urinary tract infections and complicated intra-abdominal infections. Drug Des Dev Ther. 2016;10:2379–86. https://doi.org/10.2147/DDDT.S110946.CrossRef Hidalgo JA, Vinluan CM, Antony N. Ceftazidime/avibactam: a novel cephalosporin/nonbeta-lactam beta-lactamase inhibitor for the treatment of complicated urinary tract infections and complicated intra-abdominal infections. Drug Des Dev Ther. 2016;10:2379–86. https://​doi.​org/​10.​2147/​DDDT.​S110946.CrossRef
42.
go back to reference Daniel GW, McClellan MB, Schneider M, Qian J, Lavezzari G, deGraffenreid E. Value-based strategies for encouriging new development of antimicrobial drugs. Washington, D.C.: Duke-Margolis Center for Health Policy; 2017. Daniel GW, McClellan MB, Schneider M, Qian J, Lavezzari G, deGraffenreid E. Value-based strategies for encouriging new development of antimicrobial drugs. Washington, D.C.: Duke-Margolis Center for Health Policy; 2017.
45.
47.
go back to reference Kosov M, Riefler J, Belotserkovskiy M. Community-acquired bacterial pneumonia: a challenging diagnosis in clinical trials. J Clin Stud. 2015;7:38–40. Kosov M, Riefler J, Belotserkovskiy M. Community-acquired bacterial pneumonia: a challenging diagnosis in clinical trials. J Clin Stud. 2015;7:38–40.
52.
go back to reference WHO. Model list of essential medicines, 21st list. Geneva: World Health Organization; 2019. WHO. Model list of essential medicines, 21st list. Geneva: World Health Organization; 2019.
54.
go back to reference Carmeli Y, Armstrong J, Laud PJ, Newell P, Stone G, Wardman A, et al. Ceftazidime-avibactam or best available therapy in patients with ceftazidime-resistant Enterobacteriaceae and Pseudomonas aeruginosa complicated urinary tract infections or complicated intra-abdominal infections (REPRISE): a randomised, pathogen-directed, phase 3 study. Lancet Infect Dis. 2016;16(6):661–73. https://doi.org/10.1016/S1473-3099(16)30004-4.CrossRefPubMed Carmeli Y, Armstrong J, Laud PJ, Newell P, Stone G, Wardman A, et al. Ceftazidime-avibactam or best available therapy in patients with ceftazidime-resistant Enterobacteriaceae and Pseudomonas aeruginosa complicated urinary tract infections or complicated intra-abdominal infections (REPRISE): a randomised, pathogen-directed, phase 3 study. Lancet Infect Dis. 2016;16(6):661–73. https://​doi.​org/​10.​1016/​S1473-3099(16)30004-4.CrossRefPubMed
55.
go back to reference Cadwell J. The hollow fiber infection model for antimicrobial pharmacodynamics and pharmacokinetics. Adv Pharmacoepidem Drug Safety. 2012;S1:007. Cadwell J. The hollow fiber infection model for antimicrobial pharmacodynamics and pharmacokinetics. Adv Pharmacoepidem Drug Safety. 2012;S1:007.
58.
go back to reference WHO. Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics. Geneva: World Health Organization; 2017. WHO. Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics. Geneva: World Health Organization; 2017.
62.
go back to reference US FDA. Guidance for industry: acute bacterial skin and skin structure infections: developing drugs for treatment. Silver Spring: US Food and Drug Administration; 2013. US FDA. Guidance for industry: acute bacterial skin and skin structure infections: developing drugs for treatment. Silver Spring: US Food and Drug Administration; 2013.
63.
go back to reference File TM Jr, Low DE, Eckburg PB, Talbot GH, Friedland HD, Lee J, et al. FOCUS 1: a randomized, double-blinded, multicentre, phase III trial of the efficacy and safety of ceftaroline fosamil versus ceftriaxone in community-acquired pneumonia. J Antimicrob Chemother. 2011;66(Suppl. 3):iii19–iii32. https://doi.org/10.1093/jac/dkr096.CrossRefPubMed File TM Jr, Low DE, Eckburg PB, Talbot GH, Friedland HD, Lee J, et al. FOCUS 1: a randomized, double-blinded, multicentre, phase III trial of the efficacy and safety of ceftaroline fosamil versus ceftriaxone in community-acquired pneumonia. J Antimicrob Chemother. 2011;66(Suppl. 3):iii19–iii32. https://​doi.​org/​10.​1093/​jac/​dkr096.CrossRefPubMed
64.
go back to reference Low DE, File TM Jr, Eckburg PB, Talbot GH, David Friedland H, Lee J, et al. FOCUS 2: a randomized, double-blinded, multicentre, phase III trial of the efficacy and safety of ceftaroline fosamil versus ceftriaxone in community-acquired pneumonia. J Antimicrob Chemother. 2011;66(Suppl. 3):iii33–iii44. https://doi.org/10.1093/jac/dkr097.CrossRefPubMed Low DE, File TM Jr, Eckburg PB, Talbot GH, David Friedland H, Lee J, et al. FOCUS 2: a randomized, double-blinded, multicentre, phase III trial of the efficacy and safety of ceftaroline fosamil versus ceftriaxone in community-acquired pneumonia. J Antimicrob Chemother. 2011;66(Suppl. 3):iii33–iii44. https://​doi.​org/​10.​1093/​jac/​dkr097.CrossRefPubMed
65.
go back to reference Ortiz-Ruiz G, Caballero-Lopez J, Friedland IR, Woods GL, Carides A, Protocol 018 Ertapenem Community-Acquired Pneumonia Study G. A study evaluating the efficacy, safety, and tolerability of ertapenem versus ceftriaxone for the treatment of community-acquired pneumonia in adults. Clin Infect Dis. 2002;34(8):1076–83. https://doi.org/10.1086/339543.CrossRefPubMed Ortiz-Ruiz G, Caballero-Lopez J, Friedland IR, Woods GL, Carides A, Protocol 018 Ertapenem Community-Acquired Pneumonia Study G. A study evaluating the efficacy, safety, and tolerability of ertapenem versus ceftriaxone for the treatment of community-acquired pneumonia in adults. Clin Infect Dis. 2002;34(8):1076–83. https://​doi.​org/​10.​1086/​339543.CrossRefPubMed
66.
67.
72.
go back to reference Pullman J, Champlin J, Vrooman PS Jr. Efficacy and tolerability of once-daily oral therapy with telithromycin compared with trovafloxacin for the treatment of community-acquired pneumonia in adults. Int J Clin Pract. 2003;57(5):377–84.PubMed Pullman J, Champlin J, Vrooman PS Jr. Efficacy and tolerability of once-daily oral therapy with telithromycin compared with trovafloxacin for the treatment of community-acquired pneumonia in adults. Int J Clin Pract. 2003;57(5):377–84.PubMed
Metadata
Title
Preclinical Pharmacokinetic/Pharmacodynamic Studies and Clinical Trials in the Drug Development Process of EMA-Approved Antibacterial Agents: A Review
Authors
Anselm Jorda
Markus Zeitlinger
Publication date
01-09-2020
Publisher
Springer International Publishing
Published in
Clinical Pharmacokinetics / Issue 9/2020
Print ISSN: 0312-5963
Electronic ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-020-00892-0

Other articles of this Issue 9/2020

Clinical Pharmacokinetics 9/2020 Go to the issue