遗传性眼科疾病的临床试验研究现状。

IF 1.2 4区 医学 Q4 GENETICS & HEREDITY Ophthalmic Genetics Pub Date : 2024-12-01 Epub Date: 2024-07-24 DOI:10.1080/13816810.2024.2378013
Vincent Ng, Cheuk Ying Li, Paul Cornes, Marcela Votruba
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引用次数: 0

摘要

目的:描述遗传性眼病临床试验的现状,并确定未来研究领域的分子靶点:描述遗传性眼病临床试验的现状,确定未来研究领域的分子靶点:方法:在2021年3月20日至2023年12月31日期间,对clinicaltrials.gov上的临床试验数据库进行数据分析,关键词为八种常见的遗传性眼病及其常见的分子靶点:结果:共发现 288 项涉及我们的关键词的试验,其中不包括 25 项(8.7%)未知试验(验证过期且无更新)、14 项(4.9%)提前终止的试验和 6 项(2.1%)撤销的试验。总共有 243 项(84.4%)试验被纳入其中。在这 243 项试验中,120 项试验已经完成,76 项试验仍在进行中并仍在招募人员,44 项试验仍在进行中但没有招募人员。只有 32 项(13.2%)试验公布了结果:结论:已完成试验公布结果的比例较低。结论:已完成的临床试验公布结果的比例较低,但目前和未来的遗传性眼病临床试验已确定分子靶点,前景广阔。这些试验的结果将有助于更好地了解这些疾病的治疗潜力。
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The landscape of clinical trials research in inherited ophthalmic disease.

Objective: To describe the current status of clinical trials of genetic eye diseases with identified molecular targets for future areas of research.

Method: Data analysis of the clinical trials database on clinicaltrials.gov with keywords for eight common, genetically tractable inherited eye diseases and their common molecular targets was performed during the period from 20 March 2021 to 31 December 2023.

Results: Two hundred and eighty-eight trials involving our keywords have been identified, excluding 25 (8.7%) trials which were unknown (verification expired with no update), 14 (4.9%) trials which were terminated early and 6(2.1%) trials which were withdrawn. In total there were 243 (84.4%) trials included. Out of the 243 trials, 120 trials were completed, 76 trials were active and still open to recruitment and 44 trials were active without any more recruitment on the way. There were only 32 (13.2%) trials with posted results.

Conclusions: A low percentage of results were posted for completed trials. However, current and future clinical trials in the genetic eye diseases with molecular targets identified, have a promising future. The results of these trials will enhance and allow a better understanding of the potential to develop treatments for these conditions.

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来源期刊
Ophthalmic Genetics
Ophthalmic Genetics 医学-眼科学
CiteScore
2.40
自引率
8.30%
发文量
126
审稿时长
>12 weeks
期刊介绍: Ophthalmic Genetics accepts original papers, review articles and short communications on the clinical and molecular genetic aspects of ocular diseases.
期刊最新文献
A novel frameshift variant in BCOR causes congenital nuclear cataract. Single-cell somatic copy number alteration profiling of vitreous humor seeds in retinoblastoma. Usher syndrome in the United Arab Emirates. Monoallelic missense variants in MAB21L1 cause a novel autosomal dominant microphthalmia. The landscape of clinical trials research in inherited ophthalmic disease.
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