hIL-13-PE38QQR. NeoPharm.

S Barth
{"title":"hIL-13-PE38QQR. NeoPharm.","authors":"S Barth","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>NeoPharm, under license from the NIH and the FDA, is developing a chimeric human IL-13 fused in frame to a genetically engineered truncated Pseudomonas exotoxin (PE38QQR) molecule, for its potential as an antitumor agent [266296], [281418], [290480]. NeoPharm filed an IND in 1999 for renal cell carcinoma (RCC) and glioma [319690], [325001]; an additional IND was filed in March 2000 for the treatment of glioblastoma. In December 2000, NeoPharm initiated phase I/II trials of IL-13-PE38QQR involving patients with refractory glioblastoma multiforme. This trial was being conducted by the New Approaches to Brain Tumor Therapy, a research consortium sponsored by the NCI. At that time, the first patient with brain cancer had completed treatment with IL-13-PE38QQR [393197]. In October 1999, NeoPharm initiated phase I trials of hIL-13-PE38QQR for the treatment of patients with RCC [343878]. In February 2000, Dirks & Co estimated the potential US market for hIL-13-PE38QQR to be $5.8 billion [414515].</p>","PeriodicalId":101403,"journal":{"name":"Current opinion in investigational drugs (London, England : 2000)","volume":"2 9","pages":"1309-13"},"PeriodicalIF":0.0000,"publicationDate":"2001-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in investigational drugs (London, England : 2000)","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

NeoPharm, under license from the NIH and the FDA, is developing a chimeric human IL-13 fused in frame to a genetically engineered truncated Pseudomonas exotoxin (PE38QQR) molecule, for its potential as an antitumor agent [266296], [281418], [290480]. NeoPharm filed an IND in 1999 for renal cell carcinoma (RCC) and glioma [319690], [325001]; an additional IND was filed in March 2000 for the treatment of glioblastoma. In December 2000, NeoPharm initiated phase I/II trials of IL-13-PE38QQR involving patients with refractory glioblastoma multiforme. This trial was being conducted by the New Approaches to Brain Tumor Therapy, a research consortium sponsored by the NCI. At that time, the first patient with brain cancer had completed treatment with IL-13-PE38QQR [393197]. In October 1999, NeoPharm initiated phase I trials of hIL-13-PE38QQR for the treatment of patients with RCC [343878]. In February 2000, Dirks & Co estimated the potential US market for hIL-13-PE38QQR to be $5.8 billion [414515].

hIL-13-PE38QQR。NeoPharm.
NeoPharm 公司获得了美国国立卫生研究院(NIH)和美国食品和药物管理局(FDA)的许可,正在开发一种与基因工程截短的假单胞菌外毒素(PE38QQR)分子框架融合的嵌合人 IL-13 蛋白,以挖掘其作为抗肿瘤药物的潜力 [266296]、[281418]、[290480]。1999 年,NeoPharm 公司提交了治疗肾细胞癌(RCC)和胶质瘤的 IND 申请 [319690], [325001];2000 年 3 月又提交了治疗胶质母细胞瘤的 IND 申请。2000 年 12 月,NeoPharm 启动了 IL-13-PE38QQR 的 I/II 期试验,涉及难治性多形性胶质母细胞瘤患者。该试验由 NCI 赞助的研究联盟 "脑肿瘤治疗新方法 "进行。当时,第一位脑癌患者已经完成了 IL-13-PE38QQR [393197] 的治疗。1999 年 10 月,NeoPharm 启动了治疗 RCC 患者的 hIL-13-PE38QQR I 期试验 [343878]。2000 年 2 月,Dirks & Co 公司估计 hIL-13-PE38QQR 在美国的潜在市场价值为 58 亿美元 [414515]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信