Approval status of essential therapeutic drugs for systemic sclerosis versus that of drugs for rheumatoid arthritis

Ki Won Moon, Soo-Hee Hwang, Jieun Yun, E. Lee
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Abstract

Systemic sclerosis, a rare disease characterized by chronic multisystem fibrosis, requires lifelong management, necessitating enough insurance coverage for the patient. Official drug approval is the first step to ensuring that the drug is covered by insurance. In this study, we investigated the approval status of essential therapeutic drugs for systemic sclerosis across eight countries and compared it with that of drugs for rheumatoid arthritis. The essential therapeutic drug lists for systemic sclerosis and rheumatoid arthritis were taken from the guidelines of the American College of Rheumatology and the European Alliance of Associations for Rheumatology. Official drug approval status for the selected drugs was confirmed by searching representative Internet databases from eight countries: the United States, the United Kingdom, Germany, France, Italy, Switzerland, Japan, and the Republic of Korea. A total of 21 and 16 drugs were selected for systemic sclerosis and rheumatoid arthritis, respectively. The drug approval rates of the 21 drugs for systemic sclerosis varied among countries. Most drugs used to treat pulmonary arterial hypertension, which were developed recently and are expensive, are approved by most countries; however, most older drugs—which are still essential for management of Raynaud’s phenomenon, digital ulcers, interstitial lung disease, and skin fibrosis—are not approved by most countries. By contrast, almost all of the 16 drugs used to treat rheumatoid arthritis, whether old or new, are approved by most countries. Approval rates for drugs used to treat systemic sclerosis, a rare disease, are much lower than those for drugs used to treat rheumatoid arthritis. Thus, approval rates of essential therapeutic drugs for systemic sclerosis need to improve, which will benefit patients by increasing the number of drugs covered by insurance.
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系统性硬化症基本治疗药物与类风湿关节炎药物的审批情况对比
系统性硬化症是一种以慢性多系统纤维化为特征的罕见疾病,需要终身治疗,因此必须为患者提供足够的保险。正式的药物审批是确保药物在保险范围内的第一步。在这项研究中,我们调查了八个国家系统性硬化症基本治疗药物的审批情况,并与类风湿关节炎药物的审批情况进行了比较。系统性硬化症和类风湿性关节炎的基本治疗药物清单来自美国风湿病学会和欧洲风湿病学协会联盟的指南。通过搜索八个国家(美国、英国、德国、法国、意大利、瑞士、日本和韩国)具有代表性的互联网数据库,确认了所选药物的官方药物批准状态。系统性硬化症和类风湿性关节炎分别共有 21 种和 16 种药物入选。治疗系统性硬化症的 21 种药物的批准率因国家而异。大多数用于治疗肺动脉高压的药物都获得了大多数国家的批准,这些药物开发不久,价格昂贵;然而,大多数老药--它们仍然是治疗雷诺现象、数字溃疡、间质性肺病和皮肤纤维化的必需药物--却未获得大多数国家的批准。相比之下,用于治疗类风湿性关节炎的 16 种药物,无论是老药还是新药,几乎都获得了大多数国家的批准。治疗系统性硬化症这种罕见疾病的药物的批准率远远低于治疗类风湿关节炎的药物。因此,系统性硬化症基本治疗药物的批准率需要提高,这将使更多的药物被纳入保险范围,从而使患者受益。
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CiteScore
4.10
自引率
0.00%
发文量
31
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