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晚期生物制药研发产品线的特点与趋势

Characteristics of and trends in the late-stage biopharmaceutical pipeline.

作者信息

Nagle Paul C, Nicita Christopher A, Gerdes Leslie A, Schmeichel Cynthia J

机构信息

BioMedical Insights, Inc., San Francisco, CA, USA.

出版信息

Am J Manag Care. 2008 Apr;14(4):226-9.

Abstract

OBJECTIVE

To quantify and characterize biopharmaceutical agents and new indications in late-stage development in the United States as of May 2006.

STUDY DESIGN

Review of drug development databases and other secondary sources.

METHODS

Biopharmaceutical was defined as "any biology-based therapeutic that structurally mimics compounds found within the body." Unique biopharmaceuticals, including new molecular entities or new indications in phase 2 or higher development, were identified and characterized through reviews of the literature, 5 drug development databases, a clinical trial database, and telephone inquiries with manufacturers.

RESULTS

As of May 2006, there were 111 unique biopharmaceuticals in late-stage development for 190 indications. Of 111 unique agents in the pipeline, 87 are new molecular entities, and 24 are already approved for other indications. Overall, 38 disease categories were targeted, and at least 33 physician specialties are likely to be affected. The greatest proportion of agents (43 biopharmaceuticals and 83 indications) target cancer. More than 70% of agents in the pipeline will require administration by a healthcare provider. More than 50% of the indications in the pipeline will require long-term (chronic) treatment (defined as >1 year and excludes cancer).

CONCLUSIONS

The steady growth of the US biopharmaceutical pipeline and consequent anticipated near-term approvals will increasingly affect third-party portfolio decision making. Cost of therapy, identifying the right drug for the right patient, and outcomes-based value should drive that decision process.

摘要

目的

对截至2006年5月美国处于后期研发阶段的生物制药制剂及新适应症进行量化和特征描述。

研究设计

对药物研发数据库及其他二手资料进行回顾。

方法

生物制药被定义为“任何基于生物学的治疗药物,其结构模拟体内发现的化合物”。通过文献回顾、5个药物研发数据库、一个临床试验数据库以及与制造商的电话问询,识别并描述独特的生物制药制剂,包括处于2期或更高研发阶段的新分子实体或新适应症。

结果

截至2006年5月,有111种独特的生物制药制剂处于后期研发阶段,用于190种适应症。在研发中的111种独特制剂中,87种是新分子实体,24种已被批准用于其他适应症。总体而言,涉及38个疾病类别,至少33个医师专业可能会受到影响。最大比例的制剂(43种生物制药制剂和83种适应症)针对癌症。研发中的制剂超过70%需要由医疗保健提供者给药。研发中的适应症超过50%需要长期(慢性)治疗(定义为>1年且不包括癌症)。

结论

美国生物制药研发产品线的稳步增长以及随之而来的近期预期批准将越来越多地影响第三方投资组合决策。治疗成本、为合适的患者选择合适的药物以及基于结果的价值应推动该决策过程。

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