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Antimicrob Agents Chemother. 2015 Aug;59(8):4379-86. doi: 10.1128/AAC.04652-14. Epub 2015 Apr 13.

Safety and Pharmacokinetics of Solithromycin in Subjects with Hepatic Impairment.

Author information

1
Cempra, Inc., Chapel Hill, North Carolina, USA bjamieson@cempra.com.
2
Celerion, Montreal, Quebec, Canada.
3
Cempra, Inc., Chapel Hill, North Carolina, USA.

Abstract

Solithromycin, a new macrolide and the first fluoroketolide, is in late-stage clinical development and, like older macrolides, is primarily metabolized and excreted through liver-dependent mechanisms. This study evaluated the safety and pharmacokinetics of solithromycin in patients with chronic liver disease. This open-label, multiple-dose study in subjects with hepatic impairment and in healthy control subjects (matched for age, weight, and sex) enrolled 8 Child-Pugh class A (mild), 8 class B (moderate), and 8 class C (severe) patients and 9 healthy controls. Subjects (n = 33) received one 800-mg dose on day 1 followed by once-daily doses of 400 mg on days 2 through 5. The most commonly reported adverse events were mild diarrhea and mild headache, and no significant differences were noted between hepatically impaired subjects and healthy controls. The pharmacokinetics of plasma solithromycin in subjects with mild and moderate impairment was similar to that in control subjects. In subjects with severe impairment, total exposure to solithromycin at steady state (area under the plasma concentration-time curve [AUC0-tau]) was decreased compared to that in control subjects, which may have been related to the higher body mass index of individuals in this group. No greater accumulation was noted in any hepatically impaired cohort on day 5 compared to that in control subjects. No decrease in dosage is therefore needed when administering solithromycin to patients with mild, moderate, or severe hepatic impairment. Solithromycin was well tolerated in this patient population, and no significant differences in safety, compared to healthy controls, were noted.

PMID:
25870056
PMCID:
PMC4505280
DOI:
10.1128/AAC.04652-14
[Indexed for MEDLINE]
Free PMC Article

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