Novo Nordisk ((DE:NOVA)) announced an update on their ongoing clinical study.
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Study Overview: Novo Nordisk has completed a study titled Open-label Safety Study in Adults and Adolescents With Haemophilia A With and Without FVIII Inhibitors Switching Directly From Emicizumab Prophylaxis to NNC0365-3769 (Mim8) Prophylaxis. The study aimed to assess the safety of switching patients from emicizumab to Mim8, a new treatment designed to prevent bleeding episodes in people with haemophilia A by replacing the function of the missing clotting factor VIII.
Intervention/Treatment: The study tested Mim8, a drug administered via a pen-injector under the skin. Participants could choose to receive injections weekly, biweekly, or monthly, depending on their preference and current treatment regimen.
Study Design: This Phase 3 interventional study followed a single-group model without masking, focusing on treatment as its primary purpose. Participants received Mim8 injections over a period of 6-12 months, with the number of injections varying based on dosing frequency.
Study Timeline: The study began on June 26, 2023, and was completed with the last update submitted on July 18, 2025. These dates are crucial for tracking the study’s progress and ensuring timely updates for stakeholders.
Market Implications: With the completion of this study, Novo Nordisk may see positive impacts on its stock performance and investor sentiment, as successful results could enhance its competitive position in the haemophilia treatment market. Investors will be keen to see how Mim8 compares to existing treatments and its potential to capture market share.
The study is now completed, and further details are available on the ClinicalTrials portal.