Efficacy and Safety of Single-Dose Oral Delafloxacin Compared With Intramuscular Ceftriaxone for Uncomplicated Gonorrhea Treatment: An Open-Label, Noninferiority, Phase 3, Multicenter, Randomized Study

被引:33
作者
Hook, Edward W., III [1 ]
Golden, Matthew R. [2 ]
Taylor, Stephanie N. [3 ]
Henry, Eugenia [4 ]
Tseng, Carol [4 ]
Workowski, Kimberly A. [5 ]
Swerdlow, Terri [6 ]
Nenninger, Ashley [6 ]
Cammarata, Sue [6 ]
机构
[1] Univ Alabama Birmingham, Birmingham, AL USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Louisiana State Univ, Hlth Sci Ctr, New Orleans, LA USA
[4] Firma Clin Res, Chicago, IL USA
[5] Emory Univ, Atlanta, GA 30322 USA
[6] Melinta Therapeut, 300 Tristate Int Suite 272, Lincolnshire, IL 60069 USA
关键词
DISEASES-TREATMENT-GUIDELINES; SKIN-STRUCTURE INFECTIONS; ACUTE BACTERIAL SKIN; NEISSERIA-GONORRHOEAE; ANTIMICROBIAL SUSCEPTIBILITY; DOUBLE-BLIND; RESISTANCE; WOMEN;
D O I
10.1097/OLQ.0000000000000971
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background We evaluated single oral dose of delafloxacin versus single intramuscular ceftriaxone in participants with uncomplicated urogenital gonorrhea (primary objective). Secondary objectives included the efficacy, safety, and tolerability of delafloxacin versus ceftriaxone for uncomplicated urogenital, rectal, and/or pharyngeal gonorrhea. Methods In this open-label, multicenter study, 460 participants at 25 study centers were randomized (2:1) to receive a single 900-mg oral dose of delafloxacin or 250-mg intramuscular ceftriaxone. Neisseria gonorrhoeae culture, nucleic acid amplification test, and clinical responses were evaluated. The primary efficacy end point was the urogenital microbiological cure in the urogenital microbiological intention-to-treat population; noninferiority (NI) was assessed using a 10% NI margin. Results In the urogenital microbiological intention-to-treat population, urogenital cure rates for delafloxacin were 85.1% (194/228) versus 91.0% (91/100) for ceftriaxone (95% confidence interval, -13.18% to 1.36%). Because the lower bound of the confidence interval exceeded the prespecified -10% NI margin, delafloxacin did not demonstrate NI to ceftriaxone. Treatment failures were more often associated with N. gonorrhoeae with higher delafloxacin minimum inhibitory concentration (MIC) values. In microbiologically evaluable participants, failure occurred in 1 (0.6%) of 177 urogenital infections caused by isolates with delafloxacin MICs <0.008 g/mL and 31 (64.6%) of 48 infections caused by isolates with delafloxacin MICs 0.008 g/mL. Gastrointestinal adverse events were common with 900-mg of delafloxacin and typically included mild to moderate diarrhea, flatulence, nausea, and vomiting. The most common adverse event was diarrhea in both treatment groups. Conclusions A single 900-mg dose of delafloxacin is not a reliable treatment of uncomplicated urogenital gonorrhea. Treatment failures were common in infections caused by N. gonorrhoeae with delafloxacin MICs 0.008 g/mL. Additional testing with alternative dosing regimens could be considered. ClinicalTrials.gov Identifier: NCT02015637.
引用
收藏
页码:279 / 286
页数:8
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