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1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers

BACKGROUND: Tedizolid is an oxazolidinone used to treat skin and soft-tissue infections. Rifampicin is a rifamycin antibiotic which can also treat skin and soft-tissue infections, such as those caused by Staphylococcus aureus. Tedizolid and rifampicin could be therefore used concurrently to treat in...

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Autores principales: Lee, Lawrence, Hor Hee, Kim, Paton, Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809180/
http://dx.doi.org/10.1093/ofid/ofz360.1442
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author Lee, Lawrence
Hor Hee, Kim
Paton, Nicholas
author_facet Lee, Lawrence
Hor Hee, Kim
Paton, Nicholas
author_sort Lee, Lawrence
collection PubMed
description BACKGROUND: Tedizolid is an oxazolidinone used to treat skin and soft-tissue infections. Rifampicin is a rifamycin antibiotic which can also treat skin and soft-tissue infections, such as those caused by Staphylococcus aureus. Tedizolid and rifampicin could be therefore used concurrently to treat infections. There is currently no clinical data on whether rifampicin affects tedizolid concentrations. Rifampicin is known to be an inducer of cytochrome P450s and transporters. Tedizolid is not known to be cleared by cytochrome P450s, but could be affected by other clearance mechanisms. Therefore we conducted a pharmacokinetic drug-drug interaction study to investigate whether 2 weeks of rifampicin can affect tedizolid concentrations. METHODS: We conducted a healthy volunteer study in 8 subjects. Subjects were first given linezolid 600 mg on day 1, tedizolid 200 mg on day 4, rifampicin 600 mg daily from days 5 to 19 (2 weeks of rifampicin), and an additional dose of tedizolid 200 mg on day 19. Blood was obtained at pre-dose, 1, 2, 3, 4, 5, 6, 8, and 24 hours post dose on days 4 and 19. Concentrations of tedizolid were measured using a validated liquid chromatography / mass spectrometry method. Pharmacokinetic parameters were calculated by Non-Compartmental Analyses using Phoenix WinNonLin version 8.0. The bioequivalence module was used to obtain ratios of PK parameters pre- and post-rifampicin. RESULTS: Eight subjects were included in the study. Median age (range) and weight were 34.5 (29–44) years and 64 (58.4–90.8) kg, respectively. Tedizolid was well tolerated in the study. Tedizolid AUC (0–24 hours) was reduced after 2 weeks of rifampicin (GMR 0.80, 90% confidence interval 0.73–0.88), as was Cmin (0.54, 0.44–0.66) and Cmax (0.85, 0.79–0.91). Clearance/F of tedizolid was significantly increased after rifampicin (1.35, 1.21–1.50). CONCLUSION: Rifampicin given for 2 weeks has the potential to reduce tedizolid concentrations, especially trough levels, which was reduced by 46%. Caution is recommended when using tedizolid together with rifampicin, especially when tedizolid MIC is high or treating difficult infections. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68091802019-10-28 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers Lee, Lawrence Hor Hee, Kim Paton, Nicholas Open Forum Infect Dis Abstracts BACKGROUND: Tedizolid is an oxazolidinone used to treat skin and soft-tissue infections. Rifampicin is a rifamycin antibiotic which can also treat skin and soft-tissue infections, such as those caused by Staphylococcus aureus. Tedizolid and rifampicin could be therefore used concurrently to treat infections. There is currently no clinical data on whether rifampicin affects tedizolid concentrations. Rifampicin is known to be an inducer of cytochrome P450s and transporters. Tedizolid is not known to be cleared by cytochrome P450s, but could be affected by other clearance mechanisms. Therefore we conducted a pharmacokinetic drug-drug interaction study to investigate whether 2 weeks of rifampicin can affect tedizolid concentrations. METHODS: We conducted a healthy volunteer study in 8 subjects. Subjects were first given linezolid 600 mg on day 1, tedizolid 200 mg on day 4, rifampicin 600 mg daily from days 5 to 19 (2 weeks of rifampicin), and an additional dose of tedizolid 200 mg on day 19. Blood was obtained at pre-dose, 1, 2, 3, 4, 5, 6, 8, and 24 hours post dose on days 4 and 19. Concentrations of tedizolid were measured using a validated liquid chromatography / mass spectrometry method. Pharmacokinetic parameters were calculated by Non-Compartmental Analyses using Phoenix WinNonLin version 8.0. The bioequivalence module was used to obtain ratios of PK parameters pre- and post-rifampicin. RESULTS: Eight subjects were included in the study. Median age (range) and weight were 34.5 (29–44) years and 64 (58.4–90.8) kg, respectively. Tedizolid was well tolerated in the study. Tedizolid AUC (0–24 hours) was reduced after 2 weeks of rifampicin (GMR 0.80, 90% confidence interval 0.73–0.88), as was Cmin (0.54, 0.44–0.66) and Cmax (0.85, 0.79–0.91). Clearance/F of tedizolid was significantly increased after rifampicin (1.35, 1.21–1.50). CONCLUSION: Rifampicin given for 2 weeks has the potential to reduce tedizolid concentrations, especially trough levels, which was reduced by 46%. Caution is recommended when using tedizolid together with rifampicin, especially when tedizolid MIC is high or treating difficult infections. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6809180/ http://dx.doi.org/10.1093/ofid/ofz360.1442 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Lee, Lawrence
Hor Hee, Kim
Paton, Nicholas
1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title_full 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title_fullStr 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title_full_unstemmed 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title_short 1578. Rifampicin Reduces Tedizolid Concentrations When Co-Administered in Healthy Volunteers
title_sort 1578. rifampicin reduces tedizolid concentrations when co-administered in healthy volunteers
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809180/
http://dx.doi.org/10.1093/ofid/ofz360.1442
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