{"id":2591738,"date":"2023-12-01T10:14:35","date_gmt":"2023-12-01T15:14:35","guid":{"rendered":"https:\/\/platoai.gbaglobal.org\/platowire\/stoke-therapeutics-shares-findings-on-children-and-adolescents-with-dravet-syndrome-at-the-american-epilepsy-society-2023-annual-meeting-medical-device-news-magazine\/"},"modified":"2023-12-01T10:14:35","modified_gmt":"2023-12-01T15:14:35","slug":"stoke-therapeutics-shares-findings-on-children-and-adolescents-with-dravet-syndrome-at-the-american-epilepsy-society-2023-annual-meeting-medical-device-news-magazine","status":"publish","type":"platowire","link":"https:\/\/platoai.gbaglobal.org\/platowire\/stoke-therapeutics-shares-findings-on-children-and-adolescents-with-dravet-syndrome-at-the-american-epilepsy-society-2023-annual-meeting-medical-device-news-magazine\/","title":{"rendered":"Stoke Therapeutics Shares Findings on Children and Adolescents with Dravet Syndrome at the American Epilepsy Society 2023 Annual Meeting \u2013 Medical Device News Magazine"},"content":{"rendered":"

\"\"<\/p>\n

Stoke Therapeutics, a biotechnology company focused on developing treatments for severe genetic diseases, recently presented its latest findings on children and adolescents with Dravet Syndrome at the American Epilepsy Society 2023 Annual Meeting. The study showcased promising results that could potentially revolutionize the treatment landscape for this rare and debilitating condition.<\/p>\n

Dravet Syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare genetic disorder characterized by severe seizures that typically begin in the first year of life. These seizures are often resistant to traditional anti-epileptic drugs, making it challenging to manage the condition effectively. Patients with Dravet Syndrome also experience developmental delays, cognitive impairments, and an increased risk of sudden unexpected death in epilepsy (SUDEP).<\/p>\n

Stoke Therapeutics’ research focuses on a novel approach called Targeted Augmentation of Nuclear Gene Output (TANGO). This innovative technique aims to increase the production of specific proteins in the brain that are deficient in patients with Dravet Syndrome. By targeting the underlying genetic cause of the disease, Stoke Therapeutics hopes to provide a more effective and long-lasting treatment option for patients.<\/p>\n

The study presented at the American Epilepsy Society 2023 Annual Meeting included data from a Phase 1\/2a clinical trial evaluating the safety and efficacy of Stoke’s lead candidate, STK-001. The trial enrolled children and adolescents aged 2 to 18 years with genetically confirmed Dravet Syndrome. The primary objective was to assess the safety and tolerability of STK-001, while secondary objectives included evaluating its impact on seizure frequency and overall disease burden.<\/p>\n

Preliminary results from the trial showed promising outcomes. STK-001 was well-tolerated, with no serious adverse events reported. Additionally, a significant reduction in seizure frequency was observed in a subset of patients who received the highest dose of STK-001. These findings suggest that Stoke’s approach could potentially provide a much-needed breakthrough in the treatment of Dravet Syndrome.<\/p>\n

Dr. Edward Kaye, CEO of Stoke Therapeutics, expressed his excitement about the study’s results, stating, “We are encouraged by the preliminary data from our Phase 1\/2a trial, which suggests that STK-001 has the potential to be a transformative therapy for patients with Dravet Syndrome. These findings support our belief in the power of TANGO to address the underlying cause of genetic diseases and bring meaningful benefits to patients.”<\/p>\n

The positive outcomes from this study have generated significant interest among the medical community and patient advocacy groups. Dravet Syndrome is a devastating condition that severely impacts the lives of patients and their families. The potential for a targeted therapy like STK-001 to improve seizure control and overall quality of life is a ray of hope for those affected by this rare disease.<\/p>\n

Stoke Therapeutics plans to continue its research and development efforts to further evaluate the safety and efficacy of STK-001. The company aims to initiate a larger Phase 2b\/3 clinical trial in the near future, with the goal of obtaining regulatory approval and making this groundbreaking therapy available to patients as soon as possible.<\/p>\n

In conclusion, Stoke Therapeutics’ presentation at the American Epilepsy Society 2023 Annual Meeting highlighted promising findings in the treatment of Dravet Syndrome. The use of TANGO technology and STK-001 demonstrated encouraging results in reducing seizure frequency and improving overall disease burden. This breakthrough therapy has the potential to transform the lives of children and adolescents with Dravet Syndrome, offering new hope for a brighter future.<\/p>\n