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Ensifentrine (RPL554): an investigational PDE3/4 inhibitor for the treatment of COPD

机译:Ensifentrine(RPL554):治疗COPD的研究PDE3 / 4抑制剂

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ABSTRACT Introduction: A compound that simultaneously inhibits PDE3 and PDE4 should increase airway caliber by relaxing the smooth muscle and, simultaneously, suppress airway inflammatory responses. Ensifentrine (RPL554) is considered a PDE3/4 inhibitor, although its affinity for PDE3 is 3,440 times higher than that for PDE4, that is under clinical development for the treatment of asthma and COPD and, potentially, cystic fibrosis. Areas covered: We analyze the development of this molecule from its basic pharmacology to the present clinical Phase II studies. Expert opinion: Ensifentrine is an interesting drug but there is a lack of solid studies that still does not allow us to correctly allocate this molecule in the current COPD and even asthma therapeutic armamentarium. Furthermore, apparently ensifentrine has not yet entered Phase III clinical development and, in any case, there is no reliable evidence of its ability to elicit an anti-inflammatory activity in patients with COPD or asthma. Therefore, the real anti-inflammatory profile of ensifentrine must be clarified with new studies of basic pharmacology and adequate clinical studies specifically designed. However, at present the most intriguing perspective is linked to its possible use in the treatment of cystic fibrosis, also considering the lack of valid therapeutic options for this disease.
机译:摘要介绍:同时抑制PDE3和PDE4的化合物应通过放松平滑肌,同时抑制气道炎症反应来增加气道口径。 Ensifentrine(RPL554)被认为是PDE3 / 4抑制剂,尽管其对PDE3的亲和力比PDE4的亲和力为3,440倍,这是在临床开发中用于治疗哮喘和COPD,并且可能是囊性纤维化。所涵盖的地区:我们将该分子从其基本药理学分析到本临床期II研究的发展。专家意见:Ensifentrine是一个有趣的药物,但缺乏良好的研究,仍然仍然不允许我们在目前的COPD甚至哮喘治疗骨笼中正确分配该分子。此外,显然恩森州尚未进入III期临床开发,并且在任何情况下,没有可靠的证据证明其引发COPD或哮喘患者的抗炎活动。因此,必须通过对基本药理学的新研究和专门设计的适当临床研究,阐明Ensifentrine的真正抗炎谱。然而,目前最有趣的角度与其可能在治疗囊性纤维化的情况下联系起来,考虑到缺乏这种疾病的有效治疗选择。

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