Gene-Therapy Clinical-Trial Candidate Screening for Ophthalmology enabled by Low-Cost Widefield Fundus Camera
Gene-Therapy Clinical-Trial Candidate Screening for Ophthalmology enabled by Low-Cost Widefield Fundus Camera
批准号:
10076107
负责人:
金额:
$6.28万
依托单位国家:
英国
项目类别:
Grant for R&D
财政年份:
2023
资助国家:
英国
项目状态:
已结题
起止时间:
2023 至 --
中文摘要
工程生物学的一个非常令人兴奋的应用是细胞和基因治疗的最新发展和进展。在这里,我们提出了一种破坏性的监测设备,以显著减少和简化针对眼科应用的基因治疗中临床试验患者的选择过程。基于基因治疗的眼科治疗为预防和扭转一系列无法治疗的疾病的失明提供了重要的前景。这包括更常见的疾病,如干性老年性黄斑病变和糖尿病视网膜病变(发达国家最常见的老年和工作年龄致盲原因),也包括更罕见的疾病,如脉络膜血症。实现这些基因疗法的一个关键挑战是确定合适的临床试验患者,以收集足够的数据来批准他们的使用。这是我们的项目将克服的工程生物学挑战。筛选合适的临床试验患者是一个主要挑战。即使在资源丰富的发达国家,医疗保健系统中训练有素的眼科专业知识通常也不足,无法对眼睛护理进行可靠的筛查。在选择临床试验患者时,这一问题更加严重;选择需要在适当的时间窗口确定合适的候选人,然后持续监测他们的进展。这些方法带来了重大限制,剑桥远景技术公司应该通过这个项目来避免这些限制。我们正在开发一种低成本的成像设备,它不需要训练有素的医疗专业人员的专业知识。实际上,我们正在提出一种解决方案,使基因疗法的临床试验候选选择过程自动化并显著降低经济成本。这将提供一个关键的基础设施,并在为眼科应用开发一系列基因疗法方面具有变革性。
英文摘要
An extremely exciting application of engineering biology is the recent development and advancement of cellular and gene therapy treatments. Here, we are proposing a disruptive monitoring device to significantly reduce and streamline the selection process for clinical trial patients in gene-therapy treatments targeting Ophthalmological applications.Gene-therapy based Ophthalmic treatments offer significant promise for preventing and reversing blindness in a range of untreatable disorders. This encompasses more common disorders such as Dry Age-Related Macular Disorder and Diabetic Retinopathy (most common old-age and working age causes of blindness in the developed world) to rarer diseases such as Choroideremia. A key challenge to the realisation of these gene-therapy treatments is identifying suitable clinical-trial patients to collect sufficient data to approve their use. This is the engineering biology challenge our project shall overcome.Screening for suitable clinical-trial patients is a major challenge. Even in resource-rich developed countries, there is typically insufficient bandwidth of trained Ophthalmic expertise in the healthcare system to enable reliable screening of eye-care. This issue is exacerbated for the selection of clinical-trial patients; selection requires identifying suitable candidates in appropriate time-window and then continuously monitoring their progression.These approaches present significant limitations which Cambridge Vision Technology shall obviate with this project. We are developing a low-cost imaging device which does not require the expertise of a trained medical professional. Effectively, we are proposing a solution to automate and dramatically reduce the economic cost of the clinical-trial candidate selection process for gene-therapies. This would provide a key piece of infrastructure and be transformative in enabling the development of a host of gene-therapies for Ophthalmological applications.
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