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New approaches to the modulation of inflammatory processes in airway disease models: ATS 2001, May 18-23, San Francisco

机译:调节气道疾病模型中炎症过程的新方法:ATS 2001,5月18日至23日,旧金山

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The 97th American Thoracic Society meeting proved to be an excellent meeting, providing a wealth of new information on inflammatory diseases of the airways. Once again there appeared to be an increased emphasis on chronic obstructive pulmonary disease (COPD) with most of the major drug companies concentrating a large part of their efforts in this field. An assessment of the new British Thoracic Society guidelines, which are designed to promote better management of COPD, was also presented at the meeting. Potential new treatments for inflammatory diseases of the airways including COPD were described, ranging from phase III trial data with GlaxoSmithKline's PDE4 inhibitor, Cilomilast (Ariflo?) to the development of AstraZeneca's novel dual dopamine D2-receptor/β2-adrenoreceptor agonist, Viozan?. Of particular interest was Byk Gulden's Ciclesonide, a new corticosteroid with equivalent efficacy to the market leaders but with an improved safety profile. The same company also presented data on their PDE4 inhibitor, Roflumilast, which is now in phase II/III. Bayer presented data on their PDE4 inhibitor, BAY 19-8004, in a smoking animal model and claimed greater anti-inflammatory efficacy than with a steroid. Asta Medica (now known as Elbion) also described a new potent PDE4 inhibitor, AWD 12-281, with anti-inflammatory activity. In the bronchodilator field, an analysis of data from a one-year trial with Boehringer Ingelheim's Tiotropium revealed a possible improvement in lung function in COPD patients; this needs to be confirmed in a specifically designed study. Inhibitors of p38 (c-Jun NH2-terminal kinase and syk kinase) were also discussed as anti-inflammatory agents with potential in the treatment of COPD and asthma. GlaxoSmithKline's p38 kinase inhibitor, SB 239063, appeared to be the most advanced of these with clinical data expected in two to three years. Lyn kinase was also discussed as a novel target for inflammatory airway diseases.Keywords: airway diseases, animal models, chronic obstructive pulmonary disease, new approaches, new treatments
机译:事实证明,第97届美国胸科学会是一次极好的会议,它提供了有关呼吸道炎性疾病的大量新信息。再次出现了对慢性阻塞性肺疾病(COPD)的越来越重视,大多数主要的制药公司都将大部分精力集中在这一领域。会议上还对新的英国胸科学会指南进行了评估,该指南旨在促进对COPD的更好管理。描述了潜在的包括COPD在内的气道炎性疾病的新治疗方法,从使用葛兰素史克(GlaxoSmithKline)的PDE4抑制剂Cilomilast(Ariflo?)进行的III期试验数据,到阿斯利康(AstraZeneca)新型双多巴胺D2-受体/β2-肾上腺素能受体激动剂Viozan?的开发。尤为引人关注的是Byk Gulden的Ciclesonide,一种新型皮质类固醇,其功效与市场领导者相当,但安全性得到改善。该公司还提供了其PDE4抑制剂Roflumilast的数据,该药物目前处于II / III期。拜耳在吸烟动物模型中提供了有关其PDE4抑制剂BAY 19-8004的数据,并声称其抗炎功效高于类固醇。 Asta Medica(现称为Elbion)也描述了一种新型的有效PDE4抑制剂AWD 12-281,具有抗炎活性。在支气管扩张剂领域,对勃林格殷格翰公司的噻托溴铵的一项为期一年的试验数据进行的分析显示,COPD患者的肺功能可能得到改善。这需要在专门设计的研究中得到证实。还讨论了p38的抑制剂(c-Jun NH2末端激酶和syk激酶)作为抗炎药,在治疗COPD和哮喘方面具有潜力。葛兰素史克(GlaxoSmithKline)的p38激酶抑制剂SB 239063似乎是其中最先进的,预计在两到三年内可得到临床数据。还讨论了Lyn激酶作为炎症性气道疾病的新靶标。关键词:气道疾病,动物模型,慢性阻塞性肺疾病,新方法,新疗法

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