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临床试验/NCT04926129
NCT04926129已完成不适用

Natural History of the Progression of X-Linked Retinitis Pigmentosa

NightstaRx Ltd, a Biogen Company1 个研究点 分布在 1 个国家目标入组 201 人开始时间: 2017年9月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
201
试验地点
1
主要终点
Change from Baseline in Early Treatment Diabetic Retinopathy Study (ETDRS) Best-corrected Visual Acuity (BCVA)

研究概览

简要总结

The objective of the study is to gain a better understanding of disease progression over time in participants with X-linked retinitis pigmentosa (XLRP).

详细描述

This study was previously posted by NightstaRx Ltd. In October, 2020, sponsorship of the trial was transferred to Biogen.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
7 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have documentation of a pathogenic mutation in the retinitis pigmentosa GTPase regulator (RPGR) gene.
  • Are willing and able to undergo ophthalmic examinations, as required by protocol, for up to 24 months
  • Have an ETDRS BCVA in at least 1 eye of ≥34 letters (Equivalent to Snellen ≥ 6/60 or 20/200; decimal 0.1; LogMAR 1.0).
  • Mean retinal sensitivity in the eligible eye as assessed by microperimetry:
  • Males with a mean retinal sensitivity of 68 loci ranging from ≥0.1 decibels (dB) and ≤20 dB.
  • Females with a mean retinal sensitivity of 68 loci ranging from ≥0.1 dB and ≤25 dB.
  • If female, have symptomatic disease with impairment of visual function.

排除标准

  • Have a history of amblyopia in the eligible eye.
  • Have any other significant ocular or non-ocular disease/disorder which, in the opinion of the investigator, may put the participant at risk because of participation in the study, may influence the results of the study, may influence the participant's ability to perform study diagnostic tests, or impact the participant's ability to participate in the study. This includes clinically significant cataracts.
  • Have participated in another research study involving an investigational medicinal product in the past 12 weeks or received a gene/cell-based therapy at any time previously (including but not limited to Intelligent Implant System implantation, ciliary neurotrophic factor therapy, nerve growth factor therapy).
  • NOTE: Other protocol defined Inclusion/Exclusion criteria may apply

结局指标

主要结局

Change from Baseline in Early Treatment Diabetic Retinopathy Study (ETDRS) Best-corrected Visual Acuity (BCVA)

时间窗: Up to Month 24

BCVA will be assessed for both eyes using the ETDRS visual acuity (VA) chart. BCVA test should be performed prior to pupil dilation, and distance refraction should be carried out before BCVA is measured. Initially, letters are read at a distance of 4 meters from the chart. If \<20 letters are read at 4 meters, testing at 1 meter should be performed. BCVA is to be reported as number of letters read correctly by the participant.

Change from Baseline in Retinal Sensitivity Assessed with Microperimetry

时间窗: Up to Month 24

Macular analyser integrity assessment (MAIA) microperimetry will be conducted for both eyes to assess changes in retinal sensitivity within the macula.

次要结局

  • Change from Baseline in Contrast Sensitivity(Up to Month 24)
  • Change from Baseline in Low Luminance Visual Acuity (LLVA)(Up to Month 24)
  • Change from Baseline in Health Utilities Index Mark 3 (HUI3)(Up to Month 24)
  • Change from Baseline in Intraocular Pressure as Assessed by Goldmann Applanation Tonometry(Up to Month 24)
  • Change from Baseline in Retinitis Pigmentosa (RP)-Specific Patient-Reported Outcome (PRO) Questionnaire(Up to Month 24)
  • Change from Baseline in Multi-Luminance Mobility Test (MLMT) Readings(Up to Month 24)
  • Change from Baseline in Fundus Autofluorescence (FAF)(Up to Month 24)
  • Change from Baseline in 25-item Visual Function Questionnaire (VFQ-25) Score(Up to Month 24)
  • Change from Baseline in EuroQol-5 Dimension 5-level (EQ-5D-5L)(Up to Month 24)
  • Change from Baseline in Visual Field Readings(Up to Month 24)
  • Change from Baseline in Microperimetry Readings(Up to Month 24)
  • Change from Baseline in Spectral Domain Optical Coherence Tomography (SD-OCT)(Up Month 24)
  • Change from Baseline in Fundus Photography(Up to Month 24)
  • Change from Baseline in Morphology of Eye as Assessed by Slit-lamp Examination(Up to Month 24)
  • Change from Baseline in Adaptive-Optics Scanning Laser Ophthalmoscopy (AO-SLO)(Up to Month 24)
  • Change from Baseline in Morphology of Eye as Assessed by Dilated Ophthalmoscopy(Up to Month 24)
  • Change from Baseline in Morphology of Eye as Assessed by Lens Opacities Classification System (LOCS) III Lens Grading(Up to Month 24)

研究者

发起方
NightstaRx Ltd, a Biogen Company
申办方类型
Other
责任方
Sponsor

研究点 (1)

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