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Timeliness of review and approval of new drugs in Canada from 1999 through 2001: Is progress being made?

机译:从1999年到2001年在加拿大进行新药审查和批准的及时性:是否正在取得进展?

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BACKGROUND: The median time to approval of new drugs in Canada decreased considerably in the mid-1990s, although it continued to be longer than in such countries as Australia, Sweden, the United Kingdom, and the United States. Ongoing concern about approval times pointed to a need for a further international comparison.OBJECTIVE: This study was designed to assess whether there have been continuing improvements in drug approval times in Canada relative to these other countries.METHODS: Application and approval dates of new chemical or biological substances approved for marketing from 1999 through 2001 were requested from the Canadian, Australian, and Swedish regulatory agencies. Information for the United States was derived from publications of the Pharmaceutical Research and Manufacturers of America. The regulatory agency for the United Kingdom does not release application dates, although these were the same as the Swedish application dates for most drugs approved in both countries through the centralized European Union (EU) review procedure. Application dates for drugs licensed under the EU mutual-recognition arrangement or in the United Kingdom only were requested from the relevant pharmaceutical companies.RESULTS: One hundred eighty-six new drugs were approved in >/=1 of the countries studied between January 1999 and December 2001: 17 (9.1%) in all 5 countries, 25 (13.4%) in 4, 27 (14.5%) in 3, 39 (21.0%) in 2, and 78 (41.9%) in 1. Approval times were longer in Canada than in Australia, although not significantly so (median time, 645 and 551 days, respectively). Canadian and Australian approval times were significantly longer than those in Sweden (431 days), the United Kingdom (479 days), and the United States (371 days) (P < 0.001). The annual median approval time in Canada increased in each of the 3 years. The approval times of priority-reviewed drugs in Canada were significantly longer than in the United States (median 317 vs 232 days) but significantly shorter than in Australia (509 days) (both comparisons, P < 0.001).CONCLUSIONS: Overall approval times of new drugs in Canada were longer than those in Australia, Sweden, the United Kingdom, and the United States in the period studied. The findings warrant ongoing monitoring of Canadian drug approval times.
机译:背景:在1990年代中期,加拿大批准新药的平均时间大大减少,尽管持续时间比澳大利亚,瑞典,英国和美国等国家长。目的:这项研究旨在评估加拿大相对于其他国家/地区的药物批准时间是否持续改善。方法:新化学品的申请和批准日期加拿大,澳大利亚和瑞典的监管机构要求从1999年至2001年批准将其销售的生物或生物物质。美国的信息来自《美国药物研究与制造商》的出版物。英国的监管机构未发布申请日期,尽管这些日期与瑞典通过欧盟集中审核程序在两国批准的大多数药品的申请日期相同。结果是:从1999年1月至2007年1月间,在> / = 1个研究国家/地区中批准了186种新药,这些药物是根据欧盟共同承认协议或仅在英国许可的药物的申请日期。 2001年12月:在所有5个国家中占17(9.1%),在4个国家中占25(13.4%),在3中占27(14.5%),在2中占39(21.0%),在1中占78(41.9%)。加拿大的情况比澳大利亚的情况要差得多(中位数分别为645天和551天)。加拿大和澳大利亚的批准时间明显长于瑞典(431天),英国(479天)和美国(371天)(P <0.001)。在加拿大,每年的平均批准时间在3年中每年都增加。在加拿大,优先审评药物的批准时间明显长于美国(中位时间为317天与232天),但明显短于澳大利亚(509天)(两者均比较,P <0.001)。在研究期间,加拿大的新药比澳大利亚,瑞典,英国和美国的新药更长。该发现需要对加拿大药品批准时间进行持续监控。

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