Novartis Vaccines and Diagnostics, Cambridge, MA 02139, USA.
Expert Rev Vaccines. 2013 Jan;12(1):13-30. doi: 10.1586/erv.12.140.
The first clinical trial of an MF59(®)-adjuvanted influenza vaccine (Novartis) was conducted 20 years ago in 1992. The product that emerged (Fluad(®), Novartis) was licensed first in Italy in 1997 and is now licensed worldwide in 30 countries. US licensure is expected in the coming years. By contrast, many alternative adjuvanted vaccines have failed to progress. The key decisions that allowed MF59 to succeed in such a challenging environment are highlighted here and the lessons that were learned along the way are discussed. MF59 was connected to vaccines that did not succeed and was perceived as a 'failure' before it was a success. Importantly, it never failed for safety reasons and was always well tolerated. Even when safety issues have emerged for alternative adjuvants, careful analysis of the substantial safety database for MF59 have shown that there are no significant concerns with widespread use, even in more 'sensitive' populations.
1992 年,首例 MF59(®)佐剂流感疫苗(诺华公司)的临床试验开展。该产品(Fluad(®),诺华公司)于 1997 年首先在意大利获得许可,目前在全球 30 个国家获得许可。预计未来几年将在美国获得许可。相比之下,许多其他佐剂疫苗未能取得进展。本文重点介绍了在如此具有挑战性的环境中使 MF59 取得成功的关键决策,并讨论了一路走来所获得的经验教训。MF59 最初与未能成功的疫苗相关联,并在取得成功之前被视为“失败”。重要的是,它从未因安全原因而失败,并且一直耐受性良好。即使对于替代佐剂出现了安全性问题,对 MF59 大量安全性数据的仔细分析表明,即使在更“敏感”的人群中,广泛使用也没有明显的担忧。