Sanofi (SNYNF) announced an update on their ongoing clinical study.
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Sanofi recently completed a study titled ‘National, Multicenter, Non-interventional, Prospective Study to Explore the Quality of Life of Patients With Severe Asthma Starting Treatment With Dupilumab (Dupixent®) in a Real-world Setting.’ The study aimed to evaluate the health-related quality of life (HRQoL) in adults with severe asthma treated with Dupilumab over 52 weeks, with additional assessments at 12 and 24 weeks, and to ensure safety in a real-world context.
The intervention tested was Dupilumab, a medication designed to improve the quality of life for individuals suffering from severe asthma by reducing symptoms and enhancing overall health outcomes.
This observational study followed a cohort model with a prospective time perspective, focusing on real-world effectiveness and safety without any specific allocation or masking procedures.
The study began on August 24, 2023, and was completed with the last update submitted on December 8, 2025. These dates are crucial as they mark the timeline of data collection and analysis, impacting the release of results and subsequent market reactions.
The completion of this study could positively influence Sanofi’s stock performance by demonstrating the effectiveness of Dupilumab, potentially increasing investor confidence. In the competitive landscape of asthma treatments, this could position Sanofi favorably against its peers.
The study is now completed, with further details available on the ClinicalTrials portal.
To learn more about SNYNF’s potential, visit the Sanofi drug pipeline page.