Regeneron Q2 rev up 4% to $3.68 bln, Dupixent sales rise 22% to $4.34 bln.
PorAinvest
viernes, 1 de agosto de 2025, 6:34 am ET1 min de lectura
REGN--
Dupixent, a biologic medicine for the treatment of various inflammatory diseases, saw global sales rise by 22% to $4.34 billion. This growth was supported by recent FDA approvals for bullous pemphigoid and chronic spontaneous urticaria, adding to the drug's already extensive list of indications. Meanwhile, EYLEA HD, a high-dose formulation of aflibercept, experienced a 29% surge in U.S. sales to $393 million, despite a 25% decrease in total franchise sales to $1.15 billion.
Regeneron's oncology portfolio also made significant strides. The company received FDA approval for Lynozyfic in relapsed or refractory multiple myeloma, and Libtayo (cemiplimab) secured a priority review acceptance for its use in adjuvant cutaneous squamous cell carcinoma (CSCC). Additionally, the COURAGE trial, investigating obesity treatment, presented interim data demonstrating the drug's effectiveness.
The company's financial performance was bolstered by strategic in-licensing deals and substantial shareholder returns. Regeneron returned over $2.3 billion to shareholders through share repurchases and dividends, reflecting a commitment to capital allocation that supports long-term value creation.
Regeneron's strong Q2 2025 financial results underscore the company's ability to leverage its diverse pipeline and regulatory achievements to drive revenue growth. As the company continues to invest in its manufacturing capabilities and business development, investors can expect to see further progress in its pipeline and potential for future growth.
References:
[1] https://www.stocktitan.net/news/REGN/regeneron-reports-second-quarter-2025-financial-and-operating-dcwkgplv0cqh.html
• Q2 2025 revenues up 4% to $3.68 bln • Dupixent sales rise 22% to $4.34 bln • EYLEA HD sales surge 29% to $393 mln • Lynozyfic approved for relapsed/refractory multiple myeloma • Dupixent gets FDA approval for bullous pemphigoid and CSU • Libtayo sBLA for CSCC accepted for priority review • Regeneron in-licenses dual GLP-1/GIP receptor agonist • COURAGE trial interim data show obesity treatment effectiveness
Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) reported robust financial results for the second quarter of 2025, highlighting significant revenue growth and notable regulatory achievements. The company's total revenues increased by 4% to $3.68 billion, driven by strong sales performance across key product lines.Dupixent, a biologic medicine for the treatment of various inflammatory diseases, saw global sales rise by 22% to $4.34 billion. This growth was supported by recent FDA approvals for bullous pemphigoid and chronic spontaneous urticaria, adding to the drug's already extensive list of indications. Meanwhile, EYLEA HD, a high-dose formulation of aflibercept, experienced a 29% surge in U.S. sales to $393 million, despite a 25% decrease in total franchise sales to $1.15 billion.
Regeneron's oncology portfolio also made significant strides. The company received FDA approval for Lynozyfic in relapsed or refractory multiple myeloma, and Libtayo (cemiplimab) secured a priority review acceptance for its use in adjuvant cutaneous squamous cell carcinoma (CSCC). Additionally, the COURAGE trial, investigating obesity treatment, presented interim data demonstrating the drug's effectiveness.
The company's financial performance was bolstered by strategic in-licensing deals and substantial shareholder returns. Regeneron returned over $2.3 billion to shareholders through share repurchases and dividends, reflecting a commitment to capital allocation that supports long-term value creation.
Regeneron's strong Q2 2025 financial results underscore the company's ability to leverage its diverse pipeline and regulatory achievements to drive revenue growth. As the company continues to invest in its manufacturing capabilities and business development, investors can expect to see further progress in its pipeline and potential for future growth.
References:
[1] https://www.stocktitan.net/news/REGN/regeneron-reports-second-quarter-2025-financial-and-operating-dcwkgplv0cqh.html
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