Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects
Abstract Gonorrhea is a sexually transmitted infection for which antibiotic treatment options have declined due to increasing antibiotic resistance. Zoliflodacin, an investigational oral spiropyrimidinetrione antibiotic with activity against Neisseria gonorrhoeae strains that are multidrug‐resistant...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
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Wiley
2023-05-01
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Series: | Clinical and Translational Science |
Online Access: | https://doi.org/10.1111/cts.13487 |
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author | Alison Luckey Emilie Alirol Sophie Delhomme John O'Donnell Esther Bettiol John Mueller Seamus O'Brien Jean‐Yves Gillon |
author_facet | Alison Luckey Emilie Alirol Sophie Delhomme John O'Donnell Esther Bettiol John Mueller Seamus O'Brien Jean‐Yves Gillon |
author_sort | Alison Luckey |
collection | DOAJ |
description | Abstract Gonorrhea is a sexually transmitted infection for which antibiotic treatment options have declined due to increasing antibiotic resistance. Zoliflodacin, an investigational oral spiropyrimidinetrione antibiotic with activity against Neisseria gonorrhoeae strains that are multidrug‐resistant, including to third‐generation cephalosporins, is in phase III development for uncomplicated gonorrhea. This phase I, parallel, open‐label, randomized, crossover study in healthy adults evaluated the effect of food on the pharmacokinetics of single 3 or 4 g doses of zoliflodacin administered as granules for oral suspension in the fasted state or after consumption of a standardized high‐fat meal. Forty‐seven out of 48 randomized subjects completed the study. Oral administration of zoliflodacin with food delayed the absorption rate, compared with fasted state, with time to maximum concentration (Tmax) increasing from 3 to 6 h for the 3 g dose, and 2.5 to 4 h for the 4 g dose, but had no impact on the elimination of zoliflodacin. The maximum concentration (Cmax) and area under the plasma concentration‐time curve from time 0 to 24 h (AUC(0–24)) significantly increased with food by 52% and 94% for the 3 g dose, and by 89% and 108% for the 4 g dose. Forty‐two percent of participants reported a total of 34 treatment‐emergent adverse events (TEAEs), which were all considered mild in severity. Headache was the most common TEAE (22/48 subjects, 45.8%) and the only TEAE reported in more than one subject. In conclusion, administration of single 3 and 4 g doses of zoliflodacin as granules for oral suspension, with a high‐fat meal was well‐tolerated and resulted in statistically significant increases in peak and overall systemic exposure to zoliflodacin. |
first_indexed | 2024-04-09T13:10:51Z |
format | Article |
id | doaj.art-06e6f3f90fcb4202b94a93a19b09741c |
institution | Directory Open Access Journal |
issn | 1752-8054 1752-8062 |
language | English |
last_indexed | 2024-04-09T13:10:51Z |
publishDate | 2023-05-01 |
publisher | Wiley |
record_format | Article |
series | Clinical and Translational Science |
spelling | doaj.art-06e6f3f90fcb4202b94a93a19b09741c2023-05-12T07:05:38ZengWileyClinical and Translational Science1752-80541752-80622023-05-0116577078010.1111/cts.13487Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjectsAlison Luckey0Emilie Alirol1Sophie Delhomme2John O'Donnell3Esther Bettiol4John Mueller5Seamus O'Brien6Jean‐Yves Gillon7GARDP Geneva SwitzerlandGARDP Geneva SwitzerlandDNDi Geneva SwitzerlandEntasis Therapeutics Waltham Massachusetts USAGARDP Geneva SwitzerlandEntasis Therapeutics Waltham Massachusetts USAGARDP Geneva SwitzerlandDNDi Geneva SwitzerlandAbstract Gonorrhea is a sexually transmitted infection for which antibiotic treatment options have declined due to increasing antibiotic resistance. Zoliflodacin, an investigational oral spiropyrimidinetrione antibiotic with activity against Neisseria gonorrhoeae strains that are multidrug‐resistant, including to third‐generation cephalosporins, is in phase III development for uncomplicated gonorrhea. This phase I, parallel, open‐label, randomized, crossover study in healthy adults evaluated the effect of food on the pharmacokinetics of single 3 or 4 g doses of zoliflodacin administered as granules for oral suspension in the fasted state or after consumption of a standardized high‐fat meal. Forty‐seven out of 48 randomized subjects completed the study. Oral administration of zoliflodacin with food delayed the absorption rate, compared with fasted state, with time to maximum concentration (Tmax) increasing from 3 to 6 h for the 3 g dose, and 2.5 to 4 h for the 4 g dose, but had no impact on the elimination of zoliflodacin. The maximum concentration (Cmax) and area under the plasma concentration‐time curve from time 0 to 24 h (AUC(0–24)) significantly increased with food by 52% and 94% for the 3 g dose, and by 89% and 108% for the 4 g dose. Forty‐two percent of participants reported a total of 34 treatment‐emergent adverse events (TEAEs), which were all considered mild in severity. Headache was the most common TEAE (22/48 subjects, 45.8%) and the only TEAE reported in more than one subject. In conclusion, administration of single 3 and 4 g doses of zoliflodacin as granules for oral suspension, with a high‐fat meal was well‐tolerated and resulted in statistically significant increases in peak and overall systemic exposure to zoliflodacin.https://doi.org/10.1111/cts.13487 |
spellingShingle | Alison Luckey Emilie Alirol Sophie Delhomme John O'Donnell Esther Bettiol John Mueller Seamus O'Brien Jean‐Yves Gillon Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects Clinical and Translational Science |
title | Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects |
title_full | Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects |
title_fullStr | Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects |
title_full_unstemmed | Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects |
title_short | Effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension: Phase I open‐label randomized cross‐over study in healthy subjects |
title_sort | effect of food on the pharmacokinetics of zoliflodacin granules for oral suspension phase i open label randomized cross over study in healthy subjects |
url | https://doi.org/10.1111/cts.13487 |
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