Settled: Patent characteristics and litigation outcomes in the pharmaceutical industry

Author:

Ahn KieferORCID,Trujillo Antonio,Gibbons Jason,Bennett Charles L.,Anderson Gerard

Publisher

Elsevier BV

Subject

Law,Economics and Econometrics,Finance

Reference24 articles.

1. Regulation and welfare: evidence from paragraph IV generic entry in the pharmaceutical industry;Branstetter;RAND J. Econ.,2016

2. Drug competitive intelligence and analytics;Cortellis;Clarivate,2022

3. Innovation in the pharmaceutical industry: New estimates of R&D costs;DiMasi;J. Health Econ.,2016

4. FDA (1998) ‘Guidance for Industry 180-Day Generic Drug Exclusivity Under the Hatch-Waxman Amendments to the Federal Food, Drug, and Cosmetic Act’, (June), pp. 1–9. Available at: 〈https://www.fda.gov/regulatory-information/search-fda-guidance-documents/180-day-generic-drug-exclusivity-under-hatch-waxman-amendments-federal-food-drug-and-cosmetic-act〉 (Accessed: 2 March 2022).

5. FDA (2021) Paragraph IV Drug Product Applications: Generic Drug Patent Challenge Notifications. Available at: 〈https://www.fda.gov/drugs/abbreviated-new-drug-application-anda/paragraph-iv-drug-product-applications-generic-drug-patent-challenge-notifications〉 (Accessed: 2 March 2022).

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