Bristol-Myers Squibb Company ((BMY)) announced an update on their ongoing clinical study.
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Study Overview: Bristol-Myers Squibb is conducting a prospective registry study titled ‘Deliver Insights in Hypertrophic Cardiomyopathy and Observational Outcomes in Real World: United States and European Prospective Registry Study.’ The study aims to assess real-world patient characteristics, treatment patterns, and outcomes in patients with symptomatic obstructive hypertrophic cardiomyopathy (oHCM) receiving mavacamten or other treatments. This research is significant as it evaluates both the safety and effectiveness of mavacamten in real-world settings across the US and Europe.
Intervention/Treatment: The study tests the drug mavacamten, designed to treat symptomatic oHCM. Participants may also receive standard care treatments such as beta-blockers, non-dihydropyridine calcium channel blockers, or disopyramide, depending on physician prescription.
Study Design: This is an observational cohort study with a prospective time perspective. It does not involve random allocation or masking, focusing instead on observing real-world outcomes over a five-year period.
Study Timeline: The study began on August 3, 2022, with an estimated completion date in 2025. The latest update was submitted on April 10, 2025. These dates are crucial for tracking the study’s progress and anticipated results.
Market Implications: The study’s findings could significantly impact Bristol-Myers Squibb’s stock performance by demonstrating mavacamten’s real-world effectiveness and safety, potentially increasing investor confidence. The results may also influence the competitive landscape in the treatment of oHCM, affecting other companies in the cardiovascular treatment market.
The study is ongoing, with further details available on the ClinicalTrials portal.