Daiichi Sankyo Company ((DSKYF)) announced an update on their ongoing clinical study.
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Study Overview: Daiichi Sankyo Company has initiated a multi-national, non-interventional study titled ‘A Study of Bempedoic Acid or Its Single-pill Combination Therapy With Ezetimibe in Patients With Primary Hypercholesterolaemia or Mixed Dyslipidaemia.’ The study aims to evaluate the efficacy and safety of bempedoic acid, alone or in combination with ezetimibe, in real-world clinical settings for patients with primary hypercholesterolaemia or mixed dyslipidaemia, particularly in Asian and Latin American populations.
Intervention/Treatment: The study focuses on the combination of bempedoic acid and ezetimibe, a drug therapy intended to manage cholesterol levels in patients diagnosed with primary hypercholesterolaemia or mixed dyslipidaemia.
Study Design: This is an observational cohort study with a prospective time perspective. It is designed to observe the effects of the drug combination in a routine clinical practice setting without any specific allocation or masking involved.
Study Timeline: The study is not yet recruiting, with the first submission date recorded as September 25, 2025. The last update was also on September 25, 2025. These dates are crucial as they mark the initiation of the study and its current status.
Market Implications: The study’s findings could significantly impact Daiichi Sankyo’s stock performance by potentially validating the effectiveness of their drug combination in new markets. Positive results might enhance investor confidence and position the company favorably against competitors in the cholesterol management sector.
The study is ongoing, with further details available on the ClinicalTrials portal.