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Time required for approval of new drugs in Canada Australia Sweden the United Kingdom and the United States in 1996-1998

机译:1996-1998年在加拿大澳大利亚瑞典英国和美国批准新药所需的时间

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摘要

BACKGROUND: The timeliness with which national regulatory agencies approve new drugs for marketing affects health care professionals and patients. An unnecessarily long approval process delays access to new medications that may improve patients' health status. The author compared drug approval times in Canada, Australia, Sweden, the United Kingdom and the United States. METHODS: Application and approval dates of new chemical or biological substances (excluding diagnostic products, and new salts, esters, dosage forms and combinations of previously approved substances) approved for marketing in the 5 countries from January 1996 to December 1998 were requested from the relevant pharmaceutical companies. Data on new drug approvals during the study period were also obtained from the national drug regulatory agencies in Canada, Australia and Sweden and from publications of the US Food and Drug Administration. RESULTS: A total of 219 new drugs were identified as being approved in at least one of the countries during the study period: 23 (10.5%) in all 5 countries, 23 (10.5%) in 4, 27 (12.3%) in 3, 42 (19.2%) in 2, and 104 (47.5%) in 1 country. By individual nation, 97 drugs were identified as being approved in Canada, 94 in Australia, 107 in Sweden, 55 in the UK and 123 in the US. Approval times in Canada and Australia were similar (medians 518 and 526 days respectively), but both countries had significantly longer approval times than Sweden (median 371 days), the UK (median 308 days) and the US (median 369 days). This pattern was consistent across all 3 years and for the 23 new drugs approved in all 5 countries during the 3-year period. Median approval times in Canada were similar in all of the reviewing divisions of Health Canada's Therapeutic Product Program (539-574 days) except the Central Nervous System Division (428 days) and the Bureau of Biologics and Radiopharmaceuticals (698 days). INTERPRETATION: Median drug approval times during 1996-1998 decreased by varying amounts from the 1995 values in all 5 countries. However, the median approval time in Canada continues to be significantly longer than the times achieved in Sweden, the UK and the US, and it remains considerably longer than Canada's own target of 355 days for all new drugs.
机译:背景:国家监管机构批准新药上市的及时性影响了医疗保健专业人员和患者。不必要的漫长审批流程会延迟使用新药,从而改善患者的健康状况。作者比较了加拿大,澳大利亚,瑞典,英国和美国的药品批准时间。方法:要求相关国家要求1996年1月至1998年12月在五个国家/地区批准销售的新化学或生物物质(不包括诊断产品,新盐,酯,剂型和先前批准的物质的组合)的申请和批准日期。制药公司。在研究期间,有关新药批准的数据也从加拿大,澳大利亚和瑞典的国家药品监管机构以及美国食品和药物管理局的出版物中获得。结果:在研究期间,至少有一个国家/地区确认了总共219种新药被批准:所有5个国家中的23种(10.5%),4种中的23种(10.5%),3种中的27种(12.3%) ,2个国家/地区中的42个(19.2%)和1个国家/地区中的104个(47.5%)。在每个国家/地区中,有97种药物在加拿大得到批准,在澳大利亚有94种,在瑞典为107种,在英国为55种,在美国为123种。加拿大和澳大利亚的批准时间相似(分别为518天和526天),但是两个国家的批准时间比瑞典(中位数371天),英国(中位数308天)和美国(中位数369天)长得多。在过去的3年中,以及在3年中所有5个国家/地区批准的23种新药,这种模式都是一致的。在加拿大卫生部治疗产品计划的所有审核部门中,加拿大的中位批准时间(539-574天)相似,除了中枢神经系统司(428天)以及生物和放射性药物局(698天)。解释:1996年至1998年期间,这5个国家的中位药物批准时间与1995年相比有所减少。但是,加拿大的平均批准时间仍比瑞典,英国和美国的批准时间长得多,并且仍比加拿大自己设定的所有新药的355天目标要长得多。

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