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Platelet profile in patients with acute bacterial skin and skin structure infections receiving tedizolid or linezolid: Findings from the phase 3 establish clinical trials

机译:接受替硝唑或利奈唑胺治疗的急性细菌性皮肤和皮肤结构感染患者的血小板谱:3期临床研究结果

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Tedizolid, the active moiety of tedizolid phosphate, is a recently approved oxazolidinone antibacterial with activity against a wide range of Gram-positive pathogens, including resistant strains such as methicillin-resistant Staphylococcus aureus. To date, 6 days of 200 mg tedizolid once daily has been shown to be noninferior to 10 days of 600 mg linezolid twice daily in two randomized, double-blind phase 3 trials (ESTABLISH-1 and ESTABLISH-2) for the treatment of patients with acute bacterial skin and skin structure infections (ABSSSIs). The intent of this study was to characterize the platelet profiles of patients receiving tedizolid relative to linezolid over the course of treatment using pooled data from these two trials. The occurrences of clinically defined and statistical analysis plan-specified reduced platelet counts were assessed at the study days 7 to 9 visit, the study days 11 to 13 visit, and the posttherapy evaluation (PTE) visit. At the study days 7 to 9 visit, incidences of reduced platelet counts were low and largely similar between the groups. The only notable difference was a lower incidence of thrombocytopenia (platelet counts, <150,000 cells/mm3) among patients who received tedizolid (3.2%) relative to those who received linezolid (5.6%). At the study days 11 to 13 visit, patients who received tedizolid had lower incidences of platelet counts of <150,000 cells/mm3 (-5.9%), <112,500 cells/mm3 (-2.4%), and <100,000 cells/mm3 (-1.9%) than patients in the linezolid group. Similar differences were noted at the PTE visit. Findings across the two phase 3 ABSSSI trials suggest that 6 days of 200 mg tedizolid daily confers a low potential for reduced platelet counts among patients with ABSSSIs. (The ESTABLISH-1 and ESTABLISH-2 trials have been registered at ClinicalTrials.gov under registration numbers NCT01170221 and NCT01421511, respectively.)
机译:替硝唑酯是磷酸替硝唑的活性部分,是最近批准的恶唑烷酮抗菌剂,对多种革兰氏阳性病原体具有活性,包括诸如耐甲氧西林金黄色葡萄球菌的耐药菌株。迄今为止,在两项随机,双盲的3期临床试验(ESTABLISH-1和ESTABLISH-2)中,每天一次200 mg替硝唑的6天每天两次优于10天600 mg利奈唑胺的10天并不差于两次患有急性细菌性皮肤和皮肤结构感染(ABSSSI)。这项研究的目的是使用这两项试验的汇总数据,对在治疗过程中接受替佐利特相对于利奈唑胺治疗的患者的血小板特征进行表征。在研究第7至9天,研究第11至13天以及治疗后评估(PTE)访问中评估了临床定义和统计分析计划指定的血小板减少的发生率。在研究的第7至9天,血小板计数降低的发生率很低,并且两组之间基本相似。唯一显着的差异是接受替佐利特治疗的患者(3.2%)的血小板减少症发生率(血小板计数,<150,000个细胞/ mm3)低于接受利奈唑胺治疗的患者(5.6%)。在研究的第11至13天,接受替佐利德的患者血小板计数的发生率较低,分别为<150,000个细胞/ mm3(-5.9%),<112,500个细胞/ mm3(-2.4%)和<100,000个细胞/ mm3(- 1.9%)。在PTE访问中发现了类似的差异。两项3期ABSSSIs试验的发现表明,每天200 mg替硝唑治疗6天,ABSSSIs患者降低血小板计数的可能性很小。 (ESTABLISH-1和ESTABLISH-2试验已分别在ClinicalTrials.gov上注册,注册号分别为NCT01170221和NCT01421511。)

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