Bradley John, Roilides Emmanuel, Tawadrous Margaret, Yan Jean Li, Soto Elena, Stone Gregory G, Kamat Shweta, Irani Paurus, England Richard
Department of Pediatrics, Rady Children's Hospital, University of California San Diego School of Medicine, San Diego, CA, USA.
3rd Department of Pediatrics, Aristotle University and Hippokration Hospital, Thessaloniki, Greece.
J Pediatric Infect Dis Soc. 2025 May 13;14(5). doi: 10.1093/jpids/piaf028.
This phase 2a study evaluated pharmacokinetics and safety of ceftazidime-avibactam (CAZ/AVI; combination dosed as fixed 4:1 ratio) in neonates and young infants with suspected/confirmed infections due to Gram-negative pathogens requiring intravenous antibiotics.
Hospitalized neonates and infants (gestational age ≥ 26 weeks to < 3 months), enrolled sequentially into 3 age cohorts, received CAZ/AVI single dose (Part A) or multiple dose every 8 h (Part B) by 2-h intravenous infusions. Infants > 28 days (Cohort 1) received CAZ/AVI 37.5 mg/kg/dose (CAZ 30 mg/kg and AVI 7.5 mg/kg). Full-term neonates ≤ 28 days (Cohort 2) and preterm neonates ≤ 28 days (Cohort 3) received 25 mg/kg/dose (CAZ 20 mg/kg and AVI 5 mg/kg). Pharmacokinetics, safety, and clinical and microbiological outcomes (Part B only) were assessed descriptively.
Forty-six patients received CAZ/AVI, 25 in Part A and 21 in Part B. Sepsis (39.1%) and urinary tract infection (15.2%) were the predominant diagnoses. Observed drug plasma-concentration time profiles were generally similar across cohorts. Overall, 23 patients (50%) had ≥ 1 adverse event (AE), 8 patients (17.4%) had ≥ 1 serious AE (SAE), and 2 patients (4.3%) died; no SAE or death was treatment related. In Part B, ≥ 80% of patients had favorable clinical and microbiological responses.
Plasma exposures after single and multiple CAZ/AVI doses in neonates and young infants < 3 months old (37.5 [30/7.5] mg/kg/dose for > 28 days; 25 [20/5] mg/kg/dose for ≤ 28 days) were similar to approved doses for older children. The safety profile of CAZ/AVI was as expected based on previous observations. Study funded by Pfizer. Trial registration: NCT04126031.
这项2a期研究评估了头孢他啶-阿维巴坦(CAZ/AVI;按4:1固定比例联合给药)在因革兰氏阴性病原体感染而疑似/确诊且需要静脉使用抗生素的新生儿和小婴儿中的药代动力学和安全性。
住院的新生儿和婴儿(胎龄≥26周至<3个月),按顺序纳入3个年龄队列,通过2小时静脉输注接受CAZ/AVI单剂量(A部分)或每8小时多次剂量(B部分)给药。>28天的婴儿(队列1)接受CAZ/AVI 37.5mg/kg/剂量(CAZ 30mg/kg和AVI 7.5mg/kg)。≤28天的足月儿(队列2)和≤28天的早产儿(队列3)接受25mg/kg/剂量(CAZ 20mg/kg和AVI 5mg/kg)。对药代动力学、安全性以及临床和微生物学结果(仅B部分)进行描述性评估。
46例患者接受了CAZ/AVI治疗,A部分25例,B部分21例。脓毒症(39.1%)和尿路感染(15.2%)是主要诊断。各队列中观察到的药物血浆浓度-时间曲线总体相似。总体而言,23例患者(50%)发生≥1次不良事件(AE),8例患者(17.4%)发生≥1次严重不良事件(SAE),2例患者(4.3%)死亡;无SAE或死亡与治疗相关。在B部分,≥80%的患者有良好的临床和微生物学反应。
3个月以下的新生儿和小婴儿单次和多次给予CAZ/AVI剂量后(>28天为37.5[30/7.5]mg/kg/剂量;≤28天为25[20/5]mg/kg/剂量)的血浆暴露量与较大儿童的批准剂量相似。基于先前观察,CAZ/AVI的安全性符合预期。由辉瑞公司资助的研究。试验注册号:NCT04126031。