Genmab's 15-minute chart: MACD Death Cross and KDJ Death Cross observed.
PorAinvest
lunes, 20 de octubre de 2025, 9:49 am ET1 min de lectura
GMAB--
Petosemtamab, Genmab’s drug, reported a 36% response rate, 6.2-month duration of response, and 4.9-month median progression-free survival in its corresponding study. However, Truist Securities noted that the OrigAMI-4 study excluded HPV-positive patients, while about 20% of those in the petosemtamab study were HPV-positive, a group that typically shows limited response to EGFR-targeted therapies. When adjusted for similar patient populations, both therapies demonstrated comparable efficacy.
The new data prompted Janssen, the pharmaceutical arm of Johnson & Johnson, to announce plans to initiate the Phase 3 OrigAMI-5 trial, which will test a combination of amivantamab, pembrolizumab, and carboplatin in first-line HPV-unrelated recurrent or metastatic head and neck squamous cell carcinoma. Truist described the new amivantamab data as a potential competitive challenge to petosemtamab but maintained its “buy” rating on Genmab with a price target of $49, unchanged from prior coverage, according to the Investing.com article.
Technically, the 15-minute chart for Genmab indicates a bearish trend. The MACD indicator crossed below its signal line, and the KDJ indicator reached a point of convergence with the 20-day moving average, both occurring at 09:45 on October 20, 2025. This configuration suggests that the stock price has the potential to continue trending downwards, with a shift in momentum towards the downside .
JNJ--
MRUS--
Based on the 15-minute chart for Genmab, the MACD indicator has recently crossed below its signal line, while the KDJ indicator has also reached a point of convergence with the 20-day moving average, both occurring at 09:45 on October 20, 2025. This technical configuration suggests that the stock price has the potential to continue trending downwards, with a shift in momentum towards the downside. Furthermore, there is a possibility that the stock price may experience a further decrease in value.
Genmab A/S (CSE:GMAB) shares fell more than 3% on Monday after new data from Johnson & Johnson’s amivantamab suggested the drug could rival Genmab and Merus N.V.’s petosemtamab in head and neck cancer treatment. The data, released as part of Johnson & Johnson’s Phase 1 OrigAMI-4 trial, showed amivantamab achieved an overall response rate of 44.7%, a duration of response of 7.2 months, and a median progression-free survival of 6.8 months in patients with second-line or later recurrent or metastatic HPV-negative head and neck squamous cell carcinoma, as reported by Investing.com.Petosemtamab, Genmab’s drug, reported a 36% response rate, 6.2-month duration of response, and 4.9-month median progression-free survival in its corresponding study. However, Truist Securities noted that the OrigAMI-4 study excluded HPV-positive patients, while about 20% of those in the petosemtamab study were HPV-positive, a group that typically shows limited response to EGFR-targeted therapies. When adjusted for similar patient populations, both therapies demonstrated comparable efficacy.
The new data prompted Janssen, the pharmaceutical arm of Johnson & Johnson, to announce plans to initiate the Phase 3 OrigAMI-5 trial, which will test a combination of amivantamab, pembrolizumab, and carboplatin in first-line HPV-unrelated recurrent or metastatic head and neck squamous cell carcinoma. Truist described the new amivantamab data as a potential competitive challenge to petosemtamab but maintained its “buy” rating on Genmab with a price target of $49, unchanged from prior coverage, according to the Investing.com article.
Technically, the 15-minute chart for Genmab indicates a bearish trend. The MACD indicator crossed below its signal line, and the KDJ indicator reached a point of convergence with the 20-day moving average, both occurring at 09:45 on October 20, 2025. This configuration suggests that the stock price has the potential to continue trending downwards, with a shift in momentum towards the downside .
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