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Usability of a novel disposable autoinjector device for ixekizumab: results from a qualitative study and an open-label clinical trial, including patient-reported experience

机译:新型一次性自动注射器用于ixekizumab的可用性:定性研究和开放标签临床试验的结果,包括患者报告的经验

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Background: Most biologic therapies for psoriasis are delivered via subcutaneous injection. Ixekizumab, an anti-interleukin 17A monoclonal antibody approved for patients with moderate-to-severe plaque psoriasis, is delivered subcutaneously via prefilled syringe or autoinjector. Here we report the results of an ixekizumab autoinjector usability study as well as the patient-reported experience with the autoinjector in a clinical trial. Methods: The usability study enrolled 49 subjects (patients with a range of autoimmune conditions or their caregivers). Subjects were randomized to a trained or untrained group and were evaluated for their ability to perform an injection successfully when provided the device and the instructions for use. In the clinical trial, 102 subjects (patients with psoriasis or their caregivers) used the autoinjector to deliver injections of ixekizumab (80 mg every 2 weeks after a starting dose of 160 mg). At weeks 0, 4, and 8, subjects completed the subcutaneous administration assessment questionnaire, which assesses the ease of use and confidence with using an injection device. Results: In the usability study, all subjects in the untrained arm performed successful injections, while two subjects in the trained arm had an injection failure. These incidences were not consistent with any pattern of issues with the device or the instructions for use. In the clinical trial, there were two injection failures of 674 total self-injections performed over 12 weeks. At the first use of the device, 95% of subjects either agreed or strongly agreed that the device was “overall easy to use”, and they felt “confident the dose was complete” according to the subcutaneous administration assessment questionnaire. Conclusion: The ixekizumab autoinjector was used successfully by patients and caregivers with or without training. Subjects using the autoinjector in a clinical trial felt it was easy to use and felt confident while using it. Trial Registration: NCT01777191.
机译:背景:大多数牛皮癣的生物疗法都是通过皮下注射进行的。 Ixekizumab是一种抗白细胞介素17A单克隆抗体,已被批准用于中度至重度斑块状牛皮癣患者,可通过预装注射器或自动注射器皮下注射。在这里,我们报告ixekizumab自动注射器可用性研究的结果,以及在临床试验中患者报告的使用自动注射器的经验。方法:可用性研究招募了49名受试者(患有各种自身免疫性疾病或其护理人员的患者)。将受试者随机分为训练有素或未经训练的组,并在提供设备和使用说明时评估其成功进行注射的能力。在临床试验中,有102位受试者(牛皮癣患者或他们的看护者)使用自动注射器进行了ixekizumab的注射(起始剂量为160 mg后,每2周注射80 mg)。在第0、4和8周,受试者完成了皮下给药评估问卷,该问卷评估了使用注射装置的易用性和信心。结果:在可用性研究中,未经训练的手臂中的所有受试者均注射成功,而经过训练的手臂中的两名受试者注射失败。这些事件与设备或使用说明中的任何问题都不符。在临床试验中,在12周内两次注射失败,共进行674次自我注射。根据皮下给药评估问卷,首次使用该设备时,有95%的受试者同意或强烈同意该设备“总体上易于使用”,并且他们感到“确信剂量已完成”。结论:ixekizumab自动注射器已在患者和护理人员中接受或未经培训而成功使用。在临床试验中使用自动注射器的受试者感到它易于使用,并且在使用时充满信心。试用注册:NCT01777191。

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