Daiichi Sankyo Company ((DSKYF)) announced an update on their ongoing clinical study.
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Study Overview: Daiichi Sankyo Company is conducting a study titled ‘A Prospective, Observational, Multicenter Study to Evaluate the Safety and Effectiveness of Mirogabalin in Chinese Adult Patients With Diabetic Peripheral Neuropathic Pain (DPNP) in Real-world Clinical Practice Setting (ReMIssion Study)’. The study aims to assess the safety and effectiveness of mirogabalin, a treatment for DPNP, in a real-world setting in China. This research is significant as it seeks to provide insights into the practical application of mirogabalin, potentially influencing treatment protocols for DPNP.
Intervention/Treatment: The study focuses on mirogabalin, although it is observational and non-interventional, meaning no drug will be provided as part of the study protocol. Participants already on mirogabalin will be observed to gather data on its real-world effectiveness and safety.
Study Design: This is an observational cohort study with a prospective time perspective. The study does not involve any allocation or masking, as it aims to observe the natural course of treatment in patients already receiving mirogabalin for DPNP.
Study Timeline: The study began on January 31, 2025, and the latest update was submitted on February 5, 2025. These dates are crucial as they mark the commencement of data collection and the most recent update, indicating the study’s progress and current status.
Market Implications: The ongoing study could have significant implications for Daiichi Sankyo’s stock performance, as positive results may boost investor confidence and market share in the treatment of diabetic peripheral neuropathic pain. The study’s outcomes could also influence the competitive landscape, particularly if mirogabalin proves to be a superior treatment option.
The study is currently recruiting, and further details are available on the ClinicalTrials portal.