2016-23年美国批准的仿制药上市趋势及其对口服固体药物市场竞争的影响

Keith M Drake, Gered Dunne, Aime Mason, Thomas G McGuire, Amie Price
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引用次数: 0

摘要

授权仿制药是品牌制造商的药品作为仿制药销售。这是第一个传统仿制药进入者在180天仿制药独占期内唯一的潜在竞争对手。然而,品牌制造商保留其授权仿制药的能力代表了一个有价值的谈判筹码,制造商可以提供第一个传统仿制药进入者,以换取更晚的仿制药竞争开始日期。通过2016-23年期间首次申请仿制药的146种口服固体药物的数据,我们发现了授权仿制药对竞争的积极和消极影响的证据。当获得授权的仿制药可用时,药店为新仿制药支付的发票价格降低了13- 18%。然而,曾经很常见的授权仿制药上市在最近几年明显下降,这可能部分是由于在品牌仿制专利诉讼和解中没有授权仿制药协议。削减这些协议可以极大地有利于药品购买者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trends In Authorized Generic Drug Launches And Their Effects On Competition In Oral-Solid Drug Markets In The US, 2016-23.

An authorized generic is a brand manufacturer's drug marketed as a generic product. It is the first traditional generic entrant's only potential competition during the 180-day generic exclusivity period. However, the brand manufacturer's ability to withhold its authorized generic represents a valuable bargaining chip that the manufacturer can offer the first traditional generic entrant in exchange for a later start date for generic competition. With data on 146 oral-solid drugs experiencing first generic entry during the period 2016-23, we found evidence for both positive and negative effects of authorized generics on competition. On-invoice prices that pharmacies paid for new generics were 13-18 percent lower when an authorized generic was available. However, authorized generic launches, which were once common, declined markedly in more recent years, which may be partly explained by no-authorized-generic agreements in brand-generic patent litigation settlements. Curtailing these agreements could greatly benefit drug purchasers.

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