申请人:Lyotropic Therapeutics, Inc.
公开号:US10314822B2
公开(公告)日:2019-06-11
Provided are low-volume, safe for injection formulations of dantrolene yielding significant advantages over the currently approved and marketed dantrolene for malignant hyperthermia (MH) threatening anesthetic crisis. Once dantrolene can be made immediately available to patients triggered of MH, the anesthesiologist will be able to focus exclusively on the management of the patient's physiologic status in this complex and evolving crisis, not on the laborious and time consuming reconstitution process of the rescue agent. The low volume, safe for injection formulations of dantrolene have significant advantages over currently used approaches to the prevention and treatment of pumphead, and other neurological, cognitive and motor dysfunction incident to iatrogenically or trauma induced situations of altered blood flow, including those incurred during surgical procedures involving CPB or related procedures, as well as those incurred during non-normothermic episodes caused iatrogenically or by disease.
与目前已获批准并在市场上销售的用于治疗恶性高热(MH)危及麻醉危机的丹曲林相比,我们提供的小剂量、安全注射型丹曲林制剂具有显著优势。一旦丹曲林可以立即用于触发恶性高热的患者,麻醉医师就能在这种复杂多变的危机中专注于患者生理状态的管理,而不是费力费时的解救剂重组过程。丹曲林的注射剂量小、安全性高,与目前使用的预防和治疗泵头及其他因先天性或外伤引起的血流改变导致的神经、认知和运动功能障碍的方法相比具有显著优势,包括在涉及 CPB 或相关程序的手术过程中发生的泵头及其他因先天性或疾病引起的非正常体温事件中发生的泵头及其他神经、认知和运动功能障碍。