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2024

Favipiravir pharmacokinetics in Thai adults with mild <scp>COVID</scp>‐19: A sub‐study of interpatient variability and ethnic differences in exposure

Prasanchaimontri, I., Manosuthi, W., Pertinez, H., Owen, A., Niyomnaitham, S., Sirijatuphat, R., . . . Chokephaibulkit, K. (2024). Favipiravir pharmacokinetics in Thai adults with mild <scp>COVID</scp>‐19: A sub‐study of interpatient variability and ethnic differences in exposure. Pharmacology Research &amp; Perspectives, 12(6). doi:10.1002/prp2.1233

DOI
10.1002/prp2.1233
Journal article

Population pharmacokinetic modeling of paired plasma-breast milk lamivudine data for estimation of infant exposure in breastfeeding mother-infant pairs.

Ojara, F. W., Kawuma, A. N., Nakalema, S., Kyohairwe, I., Nakijoba, R., Lamorde, M., . . . Waitt, C. (2024). Population pharmacokinetic modeling of paired plasma-breast milk lamivudine data for estimation of infant exposure in breastfeeding mother-infant pairs.. CPT: pharmacometrics & systems pharmacology. doi:10.1002/psp4.13274

DOI
10.1002/psp4.13274
Journal article

Ronapreve (REGN-CoV; casirivimab and imdevimab) reduces the viral burden and alters the pulmonary response to the SARS-CoV-2 Delta variant (B.1.617.2) in K18-hACE2 mice using an experimental design reflective of a treatment use case.

Tatham, L., Kipar, A., Sharp, J., Kijak, E., Herriott, J., Neary, M., . . . Owen, A. (2024). Ronapreve (REGN-CoV; casirivimab and imdevimab) reduces the viral burden and alters the pulmonary response to the SARS-CoV-2 Delta variant (B.1.617.2) in K18-hACE2 mice using an experimental design reflective of a treatment use case.. Microbiology spectrum, 12(8), e0391623. doi:10.1128/spectrum.03916-23

DOI
10.1128/spectrum.03916-23
Journal article

Hyaluronidase impacts exposures of long-acting injectable paliperidone palmitate in rodent models.

DOI
10.1101/2024.03.03.583160
Preprint

2023

Using Dynamic Oral Dosing of Rifapentine and Rifabutin to Simulate Exposure Profiles of Long-Acting Formulations in a Mouse Model of Tuberculosis Preventive Therapy

Chang, Y. S., Li, S. -Y., Pertinez, H., Betoudji, F., Lee, J., Rannard, S. P., . . . Ammerman, N. C. (2023). Using Dynamic Oral Dosing of Rifapentine and Rifabutin to Simulate Exposure Profiles of Long-Acting Formulations in a Mouse Model of Tuberculosis Preventive Therapy. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 67(7). doi:10.1128/aac.00481-23

DOI
10.1128/aac.00481-23
Journal article

Using dynamic oral dosing of rifapentine and rifabutin to simulate exposure profiles of long-acting formulations in a mouse model of tuberculosis preventive therapy.

DOI
10.1101/2023.04.12.536604
Preprint

Ronapreve (REGN-CoV; casirivimab and imdevimab) reduces the viral burden and alters the pulmonary response to the SARS-CoV-2 Delta variant (B.1.617.2) in K18-hACE2 mice using an experimental design reflective of a treatment use case.

DOI
10.1101/2022.01.23.477397
Preprint

2022

Determination of the Pharmacokinetics and Pharmacodynamics of Isoniazid, Rifampicin, Pyrazinamide and Ethambutol in a Cross-Over Cynomolgus Macaque Model of <i>Mycobacterium tuberculosis</i> Infection

Sibley, L., White, A. D., Sarfas, C., Gullick, J., Gleeson, F., Lanni, F., . . . Sharpe, S. (2022). Determination of the Pharmacokinetics and Pharmacodynamics of Isoniazid, Rifampicin, Pyrazinamide and Ethambutol in a Cross-Over Cynomolgus Macaque Model of <i>Mycobacterium tuberculosis</i> Infection. PHARMACEUTICS, 14(12). doi:10.3390/pharmaceutics14122666

DOI
10.3390/pharmaceutics14122666
Journal article

High Intrapulmonary Rifampicin and Isoniazid Concentrations Are Associated With Rapid Sputum Bacillary Clearance in Patients With Pulmonary Tuberculosis

McCallum, A. D., Pertinez, H. E., Chirambo, A. P., Sheha, I., Chasweka, M., Malamba, R., . . . Mwandumba, H. C. (2022). High Intrapulmonary Rifampicin and Isoniazid Concentrations Are Associated With Rapid Sputum Bacillary Clearance in Patients With Pulmonary Tuberculosis. CLINICAL INFECTIOUS DISEASES, 75(9), 1520-1528. doi:10.1093/cid/ciac228

DOI
10.1093/cid/ciac228
Journal article

Lack of antiviral activity of probenecid in Vero E6 cells and Syrian golden hamsters: a need for better understanding of inter-lab differences in preclinical assays.

DOI
10.1101/2022.03.03.482788
Preprint

2021

Optimal dose and safety of molnupiravir in patients with early SARS-CoV-2: a Phase I, open-label, dose-escalating, randomized controlled study

Khoo, S. H., Fitzgerald, R., Fletcher, T., Ewings, S., Jaki, T., Lyon, R., . . . Griffiths, G. (2021). Optimal dose and safety of molnupiravir in patients with early SARS-CoV-2: a Phase I, open-label, dose-escalating, randomized controlled study. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 76(12), 3286-3295. doi:10.1093/jac/dkab318

DOI
10.1093/jac/dkab318
Journal article

An open label, adaptive, phase 1 trial of high-dose oral nitazoxanide in healthy volunteers: an antiviral candidate for SARS-CoV-2

DOI
10.1101/2021.09.10.21263376
Preprint

Optimal dose and safety of molnupiravir in patients with early SARS-CoV-2: a phase 1, dose-escalating, randomised controlled study

DOI
10.1101/2021.05.03.21256309
Preprint

Pharmacokinetic modelling to estimate intracellular favipiravir ribofuranosyl-5'-triphosphate exposure to support posology for SARS-CoV-2.

Pertinez, H., Rajoli, R. K., Khoo, S. H., & Owen, A. (2021). Pharmacokinetic modelling to estimate intracellular favipiravir ribofuranosyl-5'-triphosphate exposure to support posology for SARS-CoV-2.. medRxiv. doi:10.1101/2021.01.03.21249159

DOI
10.1101/2021.01.03.21249159
Journal article

2020

Prioritisation of Anti-SARS-Cov-2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics.

Arshad, U., Pertinez, H., Box, H., Tatham, L., Rajoli, R. K., Curley, P., . . . Owen, A. (2020). Prioritisation of Anti-SARS-Cov-2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics.. Clinical pharmacology and therapeutics. doi:10.1002/cpt.1909

DOI
10.1002/cpt.1909
Journal article

Modelling of Systemic versus Pulmonary Chloroquine Exposure in Man for COVID-19 Dose Selection

Aljayyoussi, G., Rajoli, R. K. R., Pertinez, H., Pennington, S., Hong, D., O’Neill, P., . . . Biagini, G. (2020). Modelling of Systemic versus Pulmonary Chloroquine Exposure in Man for COVID-19 Dose Selection. doi:10.1101/2020.04.24.20078741

DOI
10.1101/2020.04.24.20078741
Journal article

Prioritisation of potential anti-SARS-CoV-2 drug repurposing opportunities based on ability to achieve adequate plasma and target site concentrations derived from their established human pharmacokinetics

Arshad, U., Pertinez, H., Box, H., Tatham, L., Rajoli, R. K. R., Curley, P., . . . Owen, A. (2020). Prioritisation of potential anti-SARS-CoV-2 drug repurposing opportunities based on ability to achieve adequate plasma and target site concentrations derived from their established human pharmacokinetics. doi:10.1101/2020.04.16.20068379

DOI
10.1101/2020.04.16.20068379
Journal article

2019

Regrowth of Mycobacterium tuberculosis Populations Exposed to Antibiotic Combinations Is Due to the Presence of Isoniazid and Not Bacterial Growth Rate

Hendon-Dunn, C. L., Pertinez, H., Marriott, A. A. N., Hatch, K. A., Allnutt, J. C., Davies, G., & Bacon, J. (2019). Regrowth of <i>Mycobacterium</i> <i>tuberculosis</i> Populations Exposed to Antibiotic Combinations Is Due to the Presence of Isoniazid and Not Bacterial Growth Rate. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 63(12). doi:10.1128/AAC.00570-19

DOI
10.1128/AAC.00570-19
Journal article

2018

Moxifloxacin Replacement in Contemporary Tuberculosis Drug Regimens Is Ineffective against Persistent<i> Mycobacterium tuberculosis</i> in the Cornell Mouse Model

Liu, Y., Pertinez, H., Davies, G. R., Gillespie, S. H., Coates, A. R., & Hua, Y. (2018). Moxifloxacin Replacement in Contemporary Tuberculosis Drug Regimens Is Ineffective against Persistent<i> Mycobacterium tuberculosis</i> in the Cornell Mouse Model. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 62(7). doi:10.1128/AAC.00190-18

DOI
10.1128/AAC.00190-18
Journal article

Optimal doses of rifampicin in the standard drug regimen to shorten tuberculosis treatment duration and reduce relapse by eradicating persistent bacteria

Liu, Y., Pertinez, H., Ortega-Muro, F., Alameda-Martin, L., Harrison, T., Davies, G., . . . Hu, Y. (2018). Optimal doses of rifampicin in the standard drug regimen to shorten tuberculosis treatment duration and reduce relapse by eradicating persistent bacteria. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 73(3), 724-731. doi:10.1093/jac/dkx467

DOI
10.1093/jac/dkx467
Journal article

2017

Assessment of treatment response by colony forming units, time to culture positivity and the molecular bacterial load assay compared in a mouse tuberculosis model

de Knegt, G. J., Dickinson, L., Pertinez, H., Evangelopoulos, D., McHugh, T. D., Bakker-Woudenberg, I. A. J. M., . . . de Steenwinkel, J. E. M. (2017). Assessment of treatment response by colony forming units, time to culture positivity and the molecular bacterial load assay compared in a mouse tuberculosis model. TUBERCULOSIS, 105, 113-118. doi:10.1016/j.tube.2017.05.002

DOI
10.1016/j.tube.2017.05.002
Journal article

A longitudinal modelling study estimates acute symptoms of community acquired pneumonia recover to baseline by 10 days

Wootton, D. G., Dickinson, L., Pertinez, H., Court, J., Eneje, O., Keogan, L., . . . Diggle, P. J. (2017). A longitudinal modelling study estimates acute symptoms of community acquired pneumonia recover to baseline by 10 days. European Respiratory Journal, 49(6). doi:10.1183/13993003.02170-2016

DOI
10.1183/13993003.02170-2016
Journal article

2016

A combination of clinical and genetic covariates significantly influence the metabolism of carbamazepine: potential implications for carbamazepine hypersensitivity

Yip, V. L. M., Meng, X., Maggs, J. L., Pertinez, H., Carr, D. F., Marson, A. G., . . . Pirmohamed, M. (2016). A combination of clinical and genetic covariates significantly influence the metabolism of carbamazepine: potential implications for carbamazepine hypersensitivity. London, UK.

Presentation material

Investigation of Elimination Rate, Persistent Subpopulation Removal, and Relapse Rates of Mycobacterium tuberculosis by Using Combinations of First-Line Drugs in a Modified Cornell Mouse Model

Hu, Y., Pertinez, H., Ortega-Muro, F., Alameda-Martin, L., Liu, Y., Schipani, A., . . . Coates, A. (2016). Investigation of Elimination Rate, Persistent Subpopulation Removal, and Relapse Rates of Mycobacterium tuberculosis by Using Combinations of First-Line Drugs in a Modified Cornell Mouse Model. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 60(8), 4778-4785. doi:10.1128/AAC.02548-15

DOI
10.1128/AAC.02548-15
Journal article

2015

Empirical and semi-mechanistic modelling of double-peaked pharmacokinetic profile phenomenon due to gastric emptying.

Ogungbenro, K., Pertinez, H., & Aarons, L. (2015). Empirical and semi-mechanistic modelling of double-peaked pharmacokinetic profile phenomenon due to gastric emptying.. The AAPS journal, 17(1), 227-236. doi:10.1208/s12248-014-9693-5

DOI
10.1208/s12248-014-9693-5
Journal article

2013

A physiologically based pharmacokinetic model for strontium exposure in rat.

Pertinez, H., Chenel, M., & Aarons, L. (2013). A physiologically based pharmacokinetic model for strontium exposure in rat.. Pharmaceutical research, 30(6), 1536-1552. doi:10.1007/s11095-013-0991-x

DOI
10.1007/s11095-013-0991-x
Journal article

2012

Progress curve mechanistic modeling approach for assessing time-dependent inhibition of CYP3A4.

Burt, H. J., Pertinez, H., Säll, C., Collins, C., Hyland, R., Houston, J. B., & Galetin, A. (2012). Progress curve mechanistic modeling approach for assessing time-dependent inhibition of CYP3A4.. Drug metabolism and disposition: the biological fate of chemicals, 40(9), 1658-1667. doi:10.1124/dmd.112.046078

DOI
10.1124/dmd.112.046078
Journal article

2011

Simulation of human intravenous and oral pharmacokinetics of 21 diverse compounds using physiologically based pharmacokinetic modelling.

Jones, H. M., Gardner, I. B., Collard, W. T., Stanley, P. J., Oxley, P., Hosea, N. A., . . . Cole, S. (2011). Simulation of human intravenous and oral pharmacokinetics of 21 diverse compounds using physiologically based pharmacokinetic modelling.. Clinical pharmacokinetics, 50(5), 331-347. doi:10.2165/11539680-000000000-00000

DOI
10.2165/11539680-000000000-00000
Journal article

2010