Bright Minds Biosciences Inc. ((TSE:DRUG)) announced an update on their ongoing clinical study.
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Bright Minds Biosciences Inc. is conducting an open-label Phase 2 study titled ‘An Open-Label Phase 2 Study to Evaluate the Efficacy, Safety and Tolerability of BMB-101 in Adults With Either Classic Absence Epilepsy (With or Without Eyelid Myoclonia (EEM; Jeavons Syndrome), OR Developmental Epileptic Encephalopathy (DEE)’. The study aims to assess the safety and effectiveness of BMB-101 in reducing seizure frequency in individuals with specific types of epilepsy, marking a significant step in addressing these challenging neurological conditions.
The intervention being tested is BMB-101, an experimental drug administered in liquid form at a dosage of 10 mg/ml. It is intended to be taken orally twice daily over a three-month period, targeting the reduction of seizure occurrences in the study participants.
The study follows an interventional design with a single-group assignment and no masking, focusing primarily on treatment. This straightforward approach allows for direct observation of the drug’s effects on the participants.
Key timelines for the study include a start date of May 2, 2024, with the latest update submitted on August 7, 2025. These dates are crucial as they provide a framework for the study’s progress and anticipated milestones.
The market implications of this study update could be significant for Bright Minds Biosciences Inc., potentially influencing its stock performance positively if the results demonstrate efficacy and safety. This development is also noteworthy in the context of the broader industry, where advancements in epilepsy treatment are highly competitive.
The study is currently ongoing, with further details available on the ClinicalTrials portal.