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纽普瑞克斯XOMA公司

Neuprex XOMA Corp.

作者信息

Mackin W M

机构信息

Alpha-Beta Technology Inc, One Innovation Drive, Worcester, MA 01605, USA.

出版信息

IDrugs. 1998 Oct;1(6):715-23.

PMID:18465627
Abstract

XOMA is developing Neuprex, an injectable recombinant protein fragment (rBPI-21) of the naturally-occurring bactericidal/permeability increasing (BPI) protein, for serious infections and infectious complications of trauma and surgery. Neuprex is the most advanced compound from XOMA's BPI platform. Neuprex is planning to commence a clinical trial for at least one additional indication in 1998 [293193]. Meningococcemia The lead indication for Neuprex is meningococcemia, for which phase III trials are expected to be completed in the second half of 1998 [275644]. In June 1998, Neuprex received Orphan Drug designation from the FDA for the treatment of severe meningococcal disease. XOMA is preparing components of a BLA to be submitted to the FDA as soon as the ongoing phase III trial is complete [290059]. In an open-label pilot study in 26 patients, completed in 1996, the mortality rate was 3.8% (one death) compared with 22% (12 deaths in 55 patients) of patients treated at the same medical centers from the previous two years [264164]. A 200-patient phase III trial, testing Neuprex in children with severe meningococcemia, is being carried out in the UK and North America. An independent Data Safety Monitoring Board recommended continuation of the trial following an interim analysis of the data [264164]. Post hepatectomy A phase II trial in partial hepatectomy patients has stopped enrollment at 35 patients (due to the slow rate; XOMA intends to make progress in other hepatic studies). Data from the first interim safety analysis, on twelve patients (low-dose group), suggested that patients receiving Neuprex spent less time on respirator, in the ICU and in the hospital [282257]. Antibiotic-resistant infections In vitro studies have shown that rBPI-21 can make resistant bacteria more antibiotic-susceptible and enhance the potency of a broad range of traditional antibiotics. Hence, XOMA has commenced studies to examine Neuprex in situations where infections may be resistant to antibiotics. A 21-patient open-label trial of Neuprex as an adjuvant to antibiotics in the treatment of severe intra-abdominal infections has been completed. The results showed a consistent, dose-related improvement in patient outcome as measured by time to improvement and time to fever-free status, but few resistant bacterial strains were found in this study and none that were resistant to all three antibiotics used in the study [282257]. In November 1997, XOMA began a clinical trial evaluating Neuprex as an adjunctive therapy with conventional antibiotics in bacterial lung infections in cystic fibrosis (CF) patients. A second study site was added in January 1998. The pilot study will enroll up to 24 CF patients hospitalized for acute bacterial exacerbations [264398]. Post-hemorrhagic trauma The company is initiating a phase III clinical trial to evaluate Neuprex as a treatment to prevent infections and infectious complications in patients suffering from hemorrhagic trauma [268444]. A 401-patient, phase II hemorrhagic trauma trial showed a positive overall benefit in patients receiving Neuprex versus placebo [282257]. A follow-on study in 169 patients confirmed the original dosing regimen [282257]. Bactericidal/permeability increasing protein platform BPI is a human host-defense protein discovered in 1978 by Drs Peter Elsbach & Gerrold Weiss, at New York University (NYU) Medical School. BPI occurs in neutrophils. XOMA scientists have discovered three active areas (functional domains) within the N-terminal fragment of human BPI (the amino-terminal 199 amino acid fragment). Many peptides, derived from these domains, have been identified and characterized. Five classes of bioactivity have been shown: antifungal, antibacterial, endotoxin-neutralizing, heparinneutralizing and anti-angiogenic [282257]. XOMA has succeeded in producing recombinant versions of BPI proteins but has also modified them to fine-tune their function and improve their pharmacodynamic profile [162407,183566, 184024]. XOMA is New York University's exclusive licensee for patents relating to human therapeutic and diagnostic uses of rBPI. XOMA has also built a broad patent position related to its own work with BPI [282257]. In addition, in July 1998, XOMA licensed all of Incyte's BPI-related intellectual property, adding seven patents to XOMA's portfolio, which now includes worldwide rights to all existing BPI patents [293193].

摘要

索马公司(XOMA)正在研发纽普瑞克(Neuprex),它是一种可注射的重组蛋白片段(rBPI - 21),来源于天然存在的杀菌/通透性增强蛋白(BPI),用于治疗严重感染以及创伤和手术引起的感染并发症。纽普瑞克是索马公司BPI平台中最先进的化合物。纽普瑞克计划于1998年针对至少一项额外适应症开展临床试验[293193]。

脑膜炎球菌血症

纽普瑞克的主要适应症是脑膜炎球菌血症,预计针对该适应症的III期试验将于1998年下半年完成[275644]。1998年6月,纽普瑞克获得美国食品药品监督管理局(FDA)授予的孤儿药认定,用于治疗严重的脑膜炎球菌疾病。索马公司正在准备一份生物制品许可申请(BLA)的组件,一旦正在进行的III期试验完成,就尽快提交给FDA[290059]。在1996年完成的一项针对26名患者的开放标签试验性研究中,死亡率为3.8%(1例死亡),而前两年在同一医疗中心接受治疗的患者死亡率为22%(55例患者中有12例死亡)[264164]。一项有200名患者参与的III期试验正在英国和北美进行,该试验在患有严重脑膜炎球菌血症的儿童中测试纽普瑞克。一个独立的数据安全监测委员会在对数据进行中期分析后建议继续进行该试验[264164]。

肝切除术后

一项针对部分肝切除患者的II期试验在招募了35名患者后停止(由于入组速度缓慢;索马公司打算在其他肝脏研究方面取得进展)。对12名患者(低剂量组)进行的首次中期安全性分析数据表明,接受纽普瑞克治疗的患者在使用呼吸机、入住重症监护病房(ICU)和住院的时间较短[282257]。

抗生素耐药感染

体外研究表明,rBPI - 21可使耐药细菌对抗生素更敏感,并增强多种传统抗生素的效力。因此,索马公司已开始研究在感染可能对抗生素耐药的情况下使用纽普瑞克。一项有21名患者参与的开放标签试验已完成,该试验将纽普瑞克作为抗生素辅助药物用于治疗严重的腹腔内感染。结果显示,以病情改善时间和无发热状态时间衡量,患者的治疗结果有持续的、与剂量相关的改善,但在该研究中发现的耐药菌株很少,且没有对研究中使用的所有三种抗生素都耐药的菌株[282257]。1997年11月,索马公司开始一项临床试验,评估纽普瑞克作为传统抗生素的辅助疗法用于治疗囊性纤维化(CF)患者的细菌性肺部感染。1998年1月增加了第二个研究地点。该试验性研究将招募多达24名因急性细菌性病情加重而住院的CF患者[264398]。

出血性创伤后

该公司正在启动一项III期临床试验,以评估纽普瑞克作为一种治疗方法,用于预防出血性创伤患者的感染和感染并发症[268444]。一项有401名患者参与的II期出血性创伤试验表明,接受纽普瑞克治疗的患者与接受安慰剂治疗的患者相比,总体受益呈阳性[282257]。一项针对169名患者的后续研究证实了最初的给药方案[282257]。

杀菌/通透性增强蛋白平台

BPI是一种人类宿主防御蛋白,1978年由纽约大学医学院的彼得·埃尔斯巴赫博士和杰罗尔德·韦斯博士发现。BPI存在于中性粒细胞中。索马公司的科学家在人类BPI的N端片段(氨基末端199个氨基酸片段)内发现了三个活性区域(功能域)。已鉴定并表征了许多源自这些区域的肽。已显示出五类生物活性:抗真菌、抗菌、内毒素中和、肝素中和以及抗血管生成[282257]。索马公司已成功生产出BPI蛋白的重组版本,但也对其进行了修饰,以微调其功能并改善其药效学特性[162407,183566,184024]。索马公司是纽约大学关于rBPI人类治疗和诊断用途专利的独家被许可方。索马公司还就其自身在BPI方面的工作建立了广泛的专利地位[282257]。此外,1998年7月,索马公司获得了因赛特公司(Incyte)所有与BPI相关的知识产权许可,为索马公司的专利组合增加了七项专利,该专利组合现在包括所有现有BPI专利的全球权利[293193]。

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