Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, District of Columbia, USA.
J Eval Clin Pract. 2022 Dec;28(6):1119-1126. doi: 10.1111/jep.13695. Epub 2022 May 11.
Branded drugs contribute disproportionately to high prescription drug spending. Pharmaceutical companies utilize patent extension "evergreening" techniques that contribute to high drug costs.
This article describes various patent extension techniques and analyzes the tactic of combining generic drugs with branded drugs, using metformin combinations for diabetes treatment as a case study. It examines the argument that FDCs enhance adherence and compares the cost of several branded fixed-dose combinations with the cost of their individual constituents.
MATERIALS & METHODS: We reviewed literature on patent extension techniques in both medical and marketing literature, supplemented by our own extensive files. We performed a price analysis of several branded pharmaceuticals and generically available equivalents. Prescription drug prices were determined using GoodRx.com, and prices of over-the-counter products were established based on the prices of two chain wholesalers. Patent and formulation information was taken from the FDA Orange Book: Approved Drugs with Therapeutic Equivalence Evaluations database.
"Evergreening" patent extension tactics include the sequential release of different formulations, minor dosing changes, and fixed-dose combinations (FDCs). A "new use" provides an opportunity for a company to re-patent, rebrand, and remarket one drug for multiple indications. It is unclear whether or not FDCs enhance adherence. Branded fixed-dose combinations generally cost far more than their individual constituents. FDCs that combine metformin with other drugs are an exception, often costing the same as the non-metformin component.
Patent extension tactics increase drug costs while providing little additional benefit to patients. Minor alterations in formulations or dosing may provide no clinical benefits. Many FDCs are expensive and fail to provide cost-justified improvements in clinical outcomes, compared to equivalent generic drugs that would save money while delivering an equal standard of care. Combining newer hypoglycemic drugs with metformin, a gold-standard, generic, inexpensive drug, does not appear to cost more than individual constituents but offers no clinical advantage over metformin alone.
Evergreening tactics should be reined in, as they represent significant cost to the healthcare system and to patients. Physicians and other prescribers should avoid prescribing FDCs, or slightly tweaked "new" drugs. Patented drug combinations generate profit without innovation.
品牌药物在高处方药支出中所占比例不成比例。制药公司利用专利延期“常青”技术来增加药品成本。
本文描述了各种专利延期技术,并分析了将仿制药与品牌药结合使用的策略,以糖尿病治疗中的二甲双胍组合为例。本文探讨了固定剂量复方制剂增强依从性的观点,并比较了几种品牌固定剂量复方制剂与其单一成分的成本。
我们查阅了医学和营销文献中关于专利延期技术的文献,并补充了我们自己的广泛文件。我们对几种品牌药物和可获得的等效仿制药进行了价格分析。处方药价格通过 GoodRx.com 确定,非处方药价格根据两家连锁批发商的价格确定。专利和配方信息取自 FDA 橙皮书:批准的具有治疗等效评价的药物数据库。
“常青”专利延期策略包括不同配方的顺序释放、小剂量变化和固定剂量复方制剂(FDCs)。“新用途”为公司提供了重新专利、重新品牌化和重新营销一种药物用于多种适应症的机会。FDC 是否增强了依从性还不清楚。品牌固定剂量复方制剂的价格通常远高于其单一成分。将二甲双胍与其他药物结合的 FDC 是一个例外,其价格通常与非二甲双胍成分相同。
专利延期策略增加了药物成本,而对患者的额外益处有限。配方或剂量的微小改变可能没有临床益处。许多 FDC 价格昂贵,与可节省成本并提供同等护理标准的等效仿制药相比,在改善临床结果方面没有成本效益。将新型降血糖药物与二甲双胍(一种标准、廉价的通用药物)结合使用,似乎并不比单一成分更昂贵,但与单独使用二甲双胍相比,并没有临床优势。
应限制常青策略,因为它们会给医疗保健系统和患者带来巨大成本。医生和其他处方者应避免开 FDC 或略有调整的“新药”。专利药物组合在没有创新的情况下产生利润。