The safety and efficacy of relebactam/imipenem/cilastatin in Japanese patients with complicated intra-abdominal infection or complicated urinary tract infection: A multicenter, open-label, noncomparative phase 3 study

被引:16
|
作者
Kohno, Shigeru [1 ]
Bando, Hiroyuki [2 ]
Yoneyama, Fumihiko [3 ]
Kikukawa, Hiroaki [4 ]
Kawahara, Kazuya [5 ]
Shirakawa, Masayoshi [6 ]
Aoyama, Norihiro [6 ]
Brown, Michelle [7 ]
Paschke, Amanda [7 ]
Takase, Akiko [6 ]
机构
[1] Nagasaki Univ, 1-14 Bunkyou Machi, Nagasaki, Nagasaki 8528521, Japan
[2] Ishikawa Prefectural Cent Hosp, 2-1 Kuratsukihigashi, Kanazawa, Ishikawa 9208530, Japan
[3] Nagoya Ekisaikai Hosp, Nakagawa Ku, 4-66 Shonen Cho, Nagoya, Aichi 4548502, Japan
[4] Natl Hosp Org Kumamoto Med Ctr, Chuo Ku, I-5 Ninomaru, Kumamoto, Kumamoto 8600008, Japan
[5] Kawahara Clin, 73-3 Nishimochida, Kagoshima 8995431, Japan
[6] MSD KK, Japan Dev, Chiyoda Ku, 1-13-12 Kudan Kita, Tokyo 1028667, Japan
[7] Merck & Co Inc, Global Clin Dev, Kenilworth, NJ USA
关键词
Complicated intra-abdominal infection; Complicated urinary tract infection; Japanese patient; Relebactam/imipenem/cilastatin; BETA-LACTAMASE INHIBITOR; MEROPENEM-VABORBACTAM; CEFTAZIDIME-AVIBACTAM; KLEBSIELLA-PNEUMONIAE; IN-VITRO; RELEBACTAM; COMBINATION; IMIPENEM;
D O I
10.1016/j.jiac.2020.09.032
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Relebactam, a novel class A/C beta-lactamase inhibitordeveloped as a fixed-dose combinationwith imipenem/cilastatin, restores imipenemactivity against imipenem-nonsusceptible gram-negative pathogens. Methods: This phase 3, multicenter, open-label, noncomparative study (NCT03293485) evaluated relebactam/imipenem/cilastatin (250 mg/500 mg/500 mg) dosed every 6 h for 5-14 days in Japanese patients with complicated intra-abdominal infections (cIAIs) or complicated urinary tract infections (cUTIs), including those with secondary sepsis. Sepsis was defined as an infection-induced systemic inflammatory response syndrome, with a documented positive blood culture; patients meeting these protocoldefined criteria were evaluated for efficacy against sepsis. Results: Of 83 patients enrolled, 81 patients (cIAI, n = 37; cUTI, n = 44) received >= 1 dose of study treatment. Escherichia coli was the most common baseline pathogen isolated in both patients with cIAI and cUTI. Adverse events (AEs) were reported in 74.1% (n = 60/81) of patients, and drug-related AEs occurred in 18.5% (n = 15/81). The most common AEs were diarrhea and nausea (8.6%). Serious AEs occurred in nine patients, including one death, but none were considered treatment related. The primary efficacy endpoint for patients with cIAI was clinical response at end of treatment (EOT) in the microbiologically evaluable (ME) population, and for patients with cUTI was microbiological response at EOT in the ME population. The proportion of cIAI and cUTI patients achieving favorable responses were 85.7% (n = 24/28) and 100.0% (n = 39/39), respectively. All patients with sepsis (cIAI, n = 1; cUTI, n = 5) achieved a favorable composite clinical and microbiological response at EOT. Conclusions: A favorable safety and efficacy profile for relebactam/imipenem/cilastatin was observed in Japanese patients with cIAI and cUTI. (C) 2020 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd.
引用
收藏
页码:262 / 270
页数:9
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