Johnson & Johnson Ends Development of Investigational Therapy Imaavy in Rheumatoid Arthritis Due to Study Failure
PorAinvest
viernes, 29 de agosto de 2025, 12:18 pm ET1 min de lectura
JNJ--
Imaavy, a potential key driver of top-line growth, was being studied in combination with anti-TNFα therapy. The mid-stage trial, which included difficult-to-treat patients with rheumatoid arthritis, did not show a significant improvement in outcomes when compared to the anti-TNFα therapy alone. Rheumatoid arthritis is an autoimmune disease that causes pain, swelling, and stiffness in the joints [1].
Despite the setback, Imaavy remains under evaluation for several other indications, including chronic inflammatory demyelinating polyneuropathy (CIDP), hemolytic anemia due to high-dose intravenous immunoglobulin (HDFN), wAIHA (warm autoimmune hemolytic anemia), and Sjogren's disease. The company is continuing to conduct late-stage studies for these conditions, which could potentially open up new revenue streams [1].
The discontinuation of Imaavy for rheumatoid arthritis is a strategic move by J&J, focusing its resources on more promising areas. The company's commitment to immunology and neuroscience indications underscores its long-term growth strategy. The peak sales for Imaavy, if successful in other indications, are expected to reach $5 billion [1].
References:
[1] https://www.reuters.com/business/healthcare-pharmaceuticals/jj-drops-development-combination-arthritis-drug-after-trial-setback-2025-08-28/
Johnson & Johnson has discontinued the development of Imaavy in rheumatoid arthritis due to phase IIa study failure. The combination therapy with anti-TNFα did not show sufficient evidence of a significant added benefit. Imaavy remains a potential key driver of top-line growth, with peak sales expected to reach $5 billion. J&J is evaluating the drug in several immunology and neuroscience indications, including late-stage studies for CIDP, HDFN, wAIHA, and Sjogren's disease.
Johnson & Johnson (JNJ.N) has announced that it will discontinue the development of its combination drug, Imaavy, in patients with rheumatoid arthritis. The decision follows the failure of a phase IIa trial to demonstrate sufficient evidence of a significant added benefit over existing anti-tumor necrosis factor alpha (anti-TNFα) therapy [1].Imaavy, a potential key driver of top-line growth, was being studied in combination with anti-TNFα therapy. The mid-stage trial, which included difficult-to-treat patients with rheumatoid arthritis, did not show a significant improvement in outcomes when compared to the anti-TNFα therapy alone. Rheumatoid arthritis is an autoimmune disease that causes pain, swelling, and stiffness in the joints [1].
Despite the setback, Imaavy remains under evaluation for several other indications, including chronic inflammatory demyelinating polyneuropathy (CIDP), hemolytic anemia due to high-dose intravenous immunoglobulin (HDFN), wAIHA (warm autoimmune hemolytic anemia), and Sjogren's disease. The company is continuing to conduct late-stage studies for these conditions, which could potentially open up new revenue streams [1].
The discontinuation of Imaavy for rheumatoid arthritis is a strategic move by J&J, focusing its resources on more promising areas. The company's commitment to immunology and neuroscience indications underscores its long-term growth strategy. The peak sales for Imaavy, if successful in other indications, are expected to reach $5 billion [1].
References:
[1] https://www.reuters.com/business/healthcare-pharmaceuticals/jj-drops-development-combination-arthritis-drug-after-trial-setback-2025-08-28/

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