Satellos Bioscience Inc. ((MSCLF)) announced an update on their ongoing clinical study.
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Satellos Bioscience Inc. is conducting a study titled An Open-Label Long-Term Follow-up Study of SAT-3247 in Patients With Duchenne Muscular Dystrophy (DMD) That Participated in SAT-3247-CL-101. The study aims to evaluate the long-term safety, tolerability, and potential efficacy of SAT-3247, an AAK1 inhibitor, in patients with DMD who completed a previous study (SAT-3247-CL-101). This research is significant as it seeks to provide insights into the long-term effects of SAT-3247, potentially offering a new therapeutic option for DMD patients.
The intervention being tested is SAT-3247, a drug administered orally at a dose of 60 mg in a 5-days on/2-days off regimen. Its purpose is to assess the long-term safety and efficacy in treating Duchenne Muscular Dystrophy.
The study follows an interventional design with a single-group assignment. It is open-label, meaning there is no masking, and its primary purpose is treatment. Up to 10 participants from the previous study will be enrolled.
The study began on March 4, 2025, with the latest update submitted on September 3, 2025. These dates are crucial as they indicate the study’s progress and the timeline for potential results that could impact the market.
This clinical update could influence Satellos Bioscience Inc.’s stock performance by boosting investor confidence if the results are positive. The study’s progress might also affect competitors in the DMD treatment space, potentially shifting market dynamics.
The study is ongoing, with further details available on the ClinicalTrials portal.