Viscofan SA ((GB:0MKW)) announced an update on their ongoing clinical study.
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Viscofan SA has initiated a groundbreaking clinical study titled ‘First in Human Open Label Multicentre Clinical Trial to Evaluate the Safety and Efficacy of Epicardial Implantation of Collagen Membranes With Allogeneic Adipose Derived Stem Cells in Patients With Ischaemic Left Ventricular Dysfunction Scheduled to Undergo Coronary Revascularisation Surgery.’ The study aims to assess the safety and efficacy of a novel treatment for patients at high risk of heart failure, focusing on reducing scar size and improving ventricular function.
The intervention under investigation is the VB-C01 cellularised patch, a combination product designed for surgical epicardial implantation. This patch is seeded with allogeneic adipose tissue-derived stem cells, intended to aid patients undergoing coronary revascularisation surgery.
This phase I study adopts an open-label, single-group assignment model with no masking, primarily targeting treatment outcomes. The study’s primary goal is to ensure the safety of the VB-C01 patch, with secondary objectives focusing on its efficacy.
Key dates for the study include its initial submission on April 15, 2025, and the latest update on April 24, 2025. These dates are crucial for tracking the study’s progress and ensuring transparency in its development.
For investors, this study represents a potential shift in Viscofan’s market positioning, as successful outcomes could enhance its stock performance and investor confidence. The innovative nature of the treatment could set Viscofan apart from competitors in the cardiovascular treatment space.
The study is ongoing, with further details available on the ClinicalTrials portal.