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GTI - 2501。洛鲁斯治疗公司。

GTI-2501. Lorus Therapeutics.

作者信息

Tu G C, Tu X

机构信息

Department of Pathology, Cell Biology and Anatomy, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Curr Opin Investig Drugs. 2001 Oct;2(10):1467-70.

Abstract

Lorus Therapeutics (formerly GeneSense Technologies) is developing GTI-2501, directed against the R1 component of ribonucleotide reductase, for the potential treatment of cancer [348928]. In November 2000, the company filed an IND with the FDA in preparation to begin a phase I trial in the US in the first quarter of 2001 [389975], [396537], [397960]. In March 2001, the FDA approved the IND application [402350], and in June 2001, a phase I, dose-escalating trial in patients with lymphomas or solid tumors which have not responded to standard therapy commenced in the US [412225]. The company expected the phase I trial of GTI-2501 to be completed within 12 to 15 months [420582]. In November 1999, the company reported that in preclinical trials, GTI-2501 was an effective anticancer agent when tested in standard mouse models bearing a variety of different human cancer lines including tumor cells derived from lung, breast, colon, kidney, ovary pancreas and skin cancers [348928]. Lorus received a patent from the US PTO in January 2000, covering the design and use of unique anitisense anticancer drugs, including GTI-2501 and GTI-2040 [353538]. In June 2000, the USPTO allowed a patent to specifically protect GTI-2501 [370810].

摘要

洛鲁斯治疗公司(前身为基因传感技术公司)正在研发针对核糖核苷酸还原酶R1成分的GTI-2501,用于潜在的癌症治疗[348928]。2000年11月,该公司向美国食品药品监督管理局(FDA)提交了一份研究性新药申请(IND),准备于2001年第一季度在美国开展I期试验[389975]、[396537]、[397960]。2001年3月,FDA批准了该IND申请[402350],2001年6月,一项针对对标准治疗无反应的淋巴瘤或实体瘤患者的I期剂量递增试验在美国启动[412225]。该公司预计GTI-2501的I期试验将在12至15个月内完成[420582]。1999年11月,该公司报告称,在临床前试验中,当在携带多种不同人类癌症细胞系(包括源自肺癌、乳腺癌、结肠癌、肾癌、卵巢癌、胰腺癌和皮肤癌的肿瘤细胞)的标准小鼠模型中进行测试时,GTI-2501是一种有效的抗癌药物[348928]。洛鲁斯于2000年1月获得了美国专利商标局(PTO)的一项专利,涵盖独特的反义抗癌药物(包括GTI-2501和GTI-2040)的设计和用途[353538]。2000年6月,美国专利商标局授予一项专利以专门保护GTI-2501[370810]。

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