Corey Ralph, Naderer Odin J, O'Riordan William D, Dumont Etienne, Jones Lori S, Kurtinecz Milena, Zhu John Z
Duke University Medical Center, Durham, North Carolina, USA.
GlaxoSmithKline, Research Triangle Park, North Carolina, USA
Antimicrob Agents Chemother. 2014 Nov;58(11):6518-27. doi: 10.1128/AAC.03360-14. Epub 2014 Aug 18.
GSK1322322 represents a new class of antibiotics that targets an essential bacterial enzyme required for protein maturation, peptide deformylase. This multicenter, randomized, phase IIa study compared the safety, tolerability, and efficacy of GSK1322322 at 1,500 mg twice daily (b.i.d.) with that of linezolid at 600 mg b.i.d. in patients suspected of having Gram-positive acute bacterial skin and skin structure infections (ABSSSIs). The primary endpoint was assessment of the safety of GSK1322322, and a key secondary endpoint was the number of subjects with a ≥20% decrease in lesion area from the baseline at 48 and 72 h after treatment initiation. GSK1322322 administration was associated with mild-to-moderate drug-related adverse events, most commonly, nausea, vomiting, diarrhea, and headache. Adverse events (86% versus 74%) and withdrawals (28% versus 11%) were more frequent in the GSK1322322-treated group. Treatment with GSK1322322 and linezolid was associated with ≥20% decreases from the baseline in the lesion area in 73% (36/49) and 92% (24/26) of the patients, respectively, at the 48-h assessment and in 96% (44/46) and 100% (25/25) of the patients, respectively, at the 72-h assessment. Reductions in exudate/pus, pain, and skin infection scores were comparable between the GSK1322322 and linezolid treatments. The clinical success rates within the intent-to-treat population and the per-protocol population that completed this study were 67 and 91%, respectively, in the GSK1322322-treated group and 89 and 100%, respectively, in the linezolid-treated group. These results will be used to guide dose selection in future studies with GSK1322322 to optimize its tolerability and efficacy in patients with ABSSSIs. (This study has been registered at ClinicalTrials.gov under registration no. NCT01209078 and at http://www.gsk-clinicalstudyregister.com [PDF113414].).
GSK1322322代表了一类新型抗生素,其作用靶点是蛋白质成熟所必需的一种关键细菌酶——肽脱甲酰基酶。这项多中心、随机、IIa期研究比较了每天两次服用1500毫克GSK1322322与每天两次服用600毫克利奈唑胺,对疑似革兰氏阳性急性细菌性皮肤和皮肤结构感染(ABSSSI)患者的安全性、耐受性和疗效。主要终点是评估GSK1322322的安全性,一个关键次要终点是治疗开始后48小时和72小时时,病变面积较基线减少≥20%的受试者数量。服用GSK1322322与轻度至中度药物相关不良事件有关,最常见的是恶心、呕吐、腹泻和头痛。在接受GSK1322322治疗的组中,不良事件(86%对74%)和退出研究的情况(28%对11%)更为频繁。在48小时评估时,接受GSK1322322和利奈唑胺治疗的患者中,分别有73%(36/49)和92%(24/26)的患者病变面积较基线减少≥20%;在72小时评估时,分别有96%(44/46)和100%(25/25)的患者病变面积较基线减少≥20%。GSK13