Amgen court hearing in patent lawsuit vs Sandoz over generic Prolia cancelled
PorAinvest
lunes, 29 de abril de 2024, 3:15 pm ET1 min de lectura
AMGN--
Amgen's lucrative bone drugs Prolia and Xgeva, both containing the active ingredient denosumab, have racked up impressive sales since their initial approvals in 2010. With Prolia generating over $4 billion and Xgeva bringing in $2.1 billion in 2021, it's no surprise that generic competitors are eager to enter the market [1]. However, ongoing patent litigation between Amgen and Sandoz, the manufacturer of the first approved denosumab biosimilars, is casting uncertainty on the launch timing [1].
Sandoz has obtained U.S. approvals for its biosimilars, Jubbonti and Wyost, which reference Amgen's Prolia and Xgeva, respectively [1]. These drugs treat all indications of the reference products and are interchangeable, enabling them to be substituted for the branded versions without approval from the prescriber [1]. However, legal disputes over Amgen-owned patents have hindered Sandoz from commenting on the anticipated launch timing or plans [1].
Amgen accused Sandoz of patent infringement in December 2021, claiming that the company's biosimilar candidate violates over 20 Prolia and Xgeva patents [2]. The biotechnology giant further argued that Sandoz failed to provide necessary details about its biosimilar's manufacturing process as required by law [2]. Amgen also expressed concern that an FDA approval decision could come before its relevant patents expire, potentially leading to significant financial losses [2].
The last denosumab patent is set to expire in July 2037 [1][2], providing a glimmer of hope for generic entrants. However, the ongoing legal battle between Amgen and Sandoz continues to complicate matters, leaving the future of the generic market for Prolia and Xgeva uncertain.
References:
[1] FiercePharma. (2022, February 9). Sandoz puts heat on Amgen as FDA approves first biosimilars for its bone blockbusters Prolia and Xgeva. Retrieved February 22, 2023, from https://www.fiercepharma.com/pharma/sandoz-puts-heat-amgen-fda-approval-first-biosimilars-its-bone-blockbusters-prolia-and-xgeva
[2] FiercePharma. (2022, February 11). Amgen sues Novartis' Sandoz over 21 alleged patent infringements on bone meds Prolia and Xgeva. Retrieved February 22, 2023, from https://www.fiercepharma.com/pharma/amgen-sues-novartis-sandoz-over-21-alleged-patent-infringements-bone-meds-prolia-and-xgeva
FFBC--
Amgen court hearing in patent lawsuit vs Sandoz over generic Prolia cancelled
Amgen's lucrative bone drugs Prolia and Xgeva, both containing the active ingredient denosumab, have racked up impressive sales since their initial approvals in 2010. With Prolia generating over $4 billion and Xgeva bringing in $2.1 billion in 2021, it's no surprise that generic competitors are eager to enter the market [1]. However, ongoing patent litigation between Amgen and Sandoz, the manufacturer of the first approved denosumab biosimilars, is casting uncertainty on the launch timing [1].
Sandoz has obtained U.S. approvals for its biosimilars, Jubbonti and Wyost, which reference Amgen's Prolia and Xgeva, respectively [1]. These drugs treat all indications of the reference products and are interchangeable, enabling them to be substituted for the branded versions without approval from the prescriber [1]. However, legal disputes over Amgen-owned patents have hindered Sandoz from commenting on the anticipated launch timing or plans [1].
Amgen accused Sandoz of patent infringement in December 2021, claiming that the company's biosimilar candidate violates over 20 Prolia and Xgeva patents [2]. The biotechnology giant further argued that Sandoz failed to provide necessary details about its biosimilar's manufacturing process as required by law [2]. Amgen also expressed concern that an FDA approval decision could come before its relevant patents expire, potentially leading to significant financial losses [2].
The last denosumab patent is set to expire in July 2037 [1][2], providing a glimmer of hope for generic entrants. However, the ongoing legal battle between Amgen and Sandoz continues to complicate matters, leaving the future of the generic market for Prolia and Xgeva uncertain.
References:
[1] FiercePharma. (2022, February 9). Sandoz puts heat on Amgen as FDA approves first biosimilars for its bone blockbusters Prolia and Xgeva. Retrieved February 22, 2023, from https://www.fiercepharma.com/pharma/sandoz-puts-heat-amgen-fda-approval-first-biosimilars-its-bone-blockbusters-prolia-and-xgeva
[2] FiercePharma. (2022, February 11). Amgen sues Novartis' Sandoz over 21 alleged patent infringements on bone meds Prolia and Xgeva. Retrieved February 22, 2023, from https://www.fiercepharma.com/pharma/amgen-sues-novartis-sandoz-over-21-alleged-patent-infringements-bone-meds-prolia-and-xgeva

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios